Abstract
The pathological hallmarks of Parkinson's disease (PD) are the progressive loss of dopaminergic neurons in the substantia nigra and the formation of Lewy bodies (LBs) in remaining neurons. LBs primarily consist of aggregated α-Synuclein (α-Syn). However, accumulating evidence suggests that Tau, which is associated with tauopathies such as Alzheimer’s disease (AD), progressive supranuclear palsy (PSP), and argyrophilic grain disease, is also involved in the pathophysiology of PD. A genome-wide association study (GWAS) identified MAPT, the gene encoding the Tau protein, as a risk gene for PD. Autopsy of PD patients also revealed the colocalization of Tau and α-Syn in LBs. Experimental evidence has shown that Tau interacts with α-Syn and influences the pathology of α-Syn in PD. In this review, we discuss the structure and function of Tau and provide a summary of the current evidence supporting Tau’s involvement as either an active or passive element in the pathophysiology of PD, which may provide novel targets for the early diagnosis and treatment of PD.
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Background
Parkinson’s disease (PD), one of the most common neurodegenerative diseases, is currently incurable. The prevalence and incidence of PD in industrialized countries are 1.0% in those over 60 years old and 8 to 18 per 100,000 person-years, respectively. Age is the strongest risk factor for PD (Balestrino and Schapira 2020). With global aging, PD is taking an increasing toll on medical resources, but its etiology remains unclear. Age and male sex are also independent risk factors for PD, and exposure to pesticides and traumatic brain injury increases the risk of PD. In contrast, reduced risk of PD is associated with smoking, caffeine consumption, higher serum urate concentrations, and physical activity (Ascherio and Schwarzschild 2016). In addition to environmental risk factors, genetic factors also play an important role in PD. Approximately 15% of PD patients have a family history, whereas 5–10% have monogenic forms of the disease. At least 23 loci and 19 disease-causing genes and various genetic risk factors have been identified to date (Deng et al. 2018). Variants in genes such as SNCA (synuclein alpha, encoding α-Syn), GBA (glucosylceramidase beta, encoding GBA protein), LRRK2 (leucine-rich repeat kinase 2, encoding LRRK2 protein), and MAPT (microtubule associated protein, encoding Tau) have been found to increase the risk of PD (Bras and Singleton 2009).
The progressive loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) and the formation of Lewy bodies (LBs) in the remaining neurons are pathological characteristics of PD (Arima et al. 1999; Kaur et al. 2019). The clinical features of PD manifest as motor as well as nonmotor symptoms. Resting tremor, bradykinesia, rigidity, and postural instability are the primary motor symptoms of PD (Sveinbjornsdottir 2016). Nonmotor symptoms such as depression, constipation, sleep disorders, and dementia can appear earlier and significantly affect quality of life (Chaudhuri et al. 2006). Levodopa is the mainstay treatment to alleviate motor symptoms (Reich and Savitt 2019). In recent years, deep brain stimulation (DBS) has become an optional therapeutic method for patients with advanced PD (Hacker et al. 2020; Krack et al. 2003).
Currently, several issues remain in the field of PD. First, the etiology and pathogenesis of PD remain elusive. Second, the diagnosis of PD relies on its motor symptoms. However, it is difficult to establish clinical acumen to make an early accurate diagnosis, though pathological lesions may appear decades before the onset of clinical symptoms. The establishment of early biological markers can facilitate the early diagnosis of PD. Third, pharmacologic treatment at the late stage of the disease has intractable side effects. Accordingly, there is an urgent need for disease-modifying drugs that can halt or slow the development of PD. To solve these problems, more research on the mechanisms underlying the pathophysiology of PD needs to be conducted.
LBs are mainly composed of aggregated forms of the presynaptic protein α-Synuclein (α-Syn), which is an abundant neuronal protein that localizes predominantly to presynaptic terminals (Kaur et al. 2019; Teravskis et al. 2018). α-Syn aggregates into fibrillary assemblies during the onset of PD, and the aberrant aggregation of α-Syn is considered to contribute to the pathogenesis of PD (Wakabayashi et al. 2013). However, the molecular mechanisms underlying the aggregation of α-Syn remain unknown. In 1999, Arima et al. detected colocalization of α-Syn and Tau, a predominant pathological element in Alzheimer’s disease (AD), in LBs of PD patients (Arima et al. 1999). Later, a genome-wide association study (GWAS) identified MAPT, the gene encoding Tau, as a risk gene for PD (Edwards et al. 2010; International Parkinson’s Disease Genomics Consortium et al. 2017). Since then, extensive investigations have been performed to explore the roles of Tau in PD. Researchers have also found a significant association between Tau levels in the cerebrospinal fluid (CSF) and clinical manifestations in PD patients (W. T. Hu et al. 2010). Furthermore, several in vitro and in vivo studies have explored the roles of Tau in PD (Beauchamp 2018; Shi et al. 2016; Singh et al. 2019). These findings indicate that Tau contributes to PD pathology as an underappreciated component and may provide a novel therapeutic target for PD.
PD Pathophysiology and Diagnosis
Currently, the molecular mechanisms underlying the pathophysiology of PD remain largely unknown. To date, α-Syn accumulation, mitochondrial dysfunction, oxidative stress, and excitotoxicity are thought to play crucial roles in PD pathophysiology (Kaur et al. 2019).
The accumulation of α-Syn progresses predictably throughout the brain, typically known as the Braak stage. The lesions initially begin from the dorsal motor nucleus of the glossopharyngeal and vagal nerves and the anterior olfactory nucleus. They then ascend to the brain stem and finally to the neocortex (Braak et al. 2003). The reasons why α-Syn, an intrinsically disordered protein, misfolds and deposits in the brain are still obscure. The currently accepted explanation is imbalance between its synthesis and clearance (Afitska et al. 2019; Ghosh et al. 2017; Mehra et al. 2019). SNCA gene duplication, triplication, or mutation aggravates the accumulation of misfolded α-Syn (Chartier-Harlin et al. 2004; Conway et al. 1998; Ross et al. 2008). Moreover, the collapse of any pathways involved in α-Syn clearance and degradation results in the accumulation of α-Syn (Cuervo 2004; McNaught et al. 2002). For instance, disruption of the lysosomal degradation pathway promotes the formation of α-Syn inclusions in cells (Desplats et al. 2009).
Oxidative stress and mitochondrial dysfunction are also closely associated with PD pathophysiology (Hemmati-Dinarvand et al. 2019). Oxidative stress is a noxious condition induced by an imbalance between reactive oxygen species (ROS) production and detoxification. It ultimately leads to impairment of cellular function (Cenini et al. 2019). It is widely accepted that the mitochondrial respiratory chain is the primary source of ROS. Mitochondrial dysfunction can lead to a decline in energy production, generation of ROS, and induction of stress-induced apoptosis (Subramaniam and Chesselet 2013). On the one hand, mutations in some genes (such as SNCA and LRRK2) and mitochondrial DNA can disrupt the fission and fusion of mitochondria and contribute to mitochondrial dysfunction and the development of PD (Bose and Beal 2016; Nguyen et al. 2019). On the other hand, α-Syn fibrils can induce mitochondrial membrane depolarization, cytochrome C release, and mitochondrial fragmentation (Grassi et al. 2018). It has also been reported that mitochondrial oxidative stress leads to the accumulation of oxidized dopamine, resulting in lysosomal dysfunction and α-Syn accumulation (Burbulla et al. 2017).
It is hypothesized that neural hyperactivity at the early stages of PD can lead to pathophysiological degeneration (Jamwal and Kumar 2019). Glutamate is the most abundant excitatory neurotransmitter in the central nervous system, and alteration of glutamate homeostasis results in neurotoxic or excitotoxic events. One of the pathophysiological hallmarks of PD is the excessive release of glutamate into the SNpc, which activates ionotropic glutamate receptors and initiates the influx of Ca2+ ions (Himmelberg et al. 2018). This triggers a variety of destructive cascades. For example, visual stimulation increased neural activity and excitotoxicity in a Drosophila model of early-onset PD (Himmelberg et al. 2018). Furthermore, Yamada and coworkers found that elevated neuronal activity increased α-Syn release (Yamada and Iwatsubo 2018). These results indicate that neuronal excitotoxicity plays a vital role in the pathophysiology of PD.
PD diagnosis is based on the presence of bradykinesia and either resting tremor or rigidity and the absence of features from the history or examination, suggesting an alternative cause of parkinsonism (Reich and Savitt 2019). A panel of diseases or factors (such as PD, multiple system atrophy, and drug-induced Parkinsonism) can cause parkinsonism, a clinical syndrome including bradykinesia, cogwheel rigidity, resting tremor, slow shuffling gait, and imbalance (Hayes 2019). Because of its heterogeneous clinical manifestations, the diagnosis of PD is not easy. Therefore, it is essential to understand the molecular mechanisms of PD to promote diagnostic advances in the future.
Tau Structure and Functions
Tau is encoded by the MAPT gene located on the long arm of chromosome 17 at 17q21 in humans. Alternative splicing of exons 2, 3, and 10 generates six Tau isoforms differing by one or two short inserts at the N-terminus (0 N, 1 N, and 2 N) and either three or four microtubule-binding repeat domains at the C-terminus (3R and 4R) (Goedert et al. 1989). Different Tau isoforms are expressed during development and in diseases. In the human fetal brain, only the shortest isoform of Tau is expressed; the mature brain expresses all six isoforms. Tau is mainly expressed in neurons but can also be detected in astrocytes and oligodendrocytes (Mietelska-Porowska et al. 2014). The N-terminal region of the protein contains a glycine-rich sequence, followed by two highly acidic regions and two proline-rich regions (P1 and P2); the remainder of the protein contains microtubule-binding domains and a short C-terminal region (Lee et al. 1988). As a member of the intrinsically disordered protein family, Tau shares many similarities with α-Syn. They are both abundant brain proteins with prion-like properties, as they can misfold, seed, and spread the misfolded conformation to typical monomeric forms of each protein (Vasili et al. 2019). Furthermore, an in vivo study demonstrated that Tau and α-Syn can accelerate each other’s aggregation, suggesting that Tau may be involved in the aggregation of α-Syn (Giasson 2003).
The physiological function of Tau is poorly understood. It was demonstrated to promote microtubule polymerization by interacting with the C-terminus of tubulin and driving tubulin assembly into microtubules, forming the cytoskeleton in neurons and defining neuronal morphology (Cleveland et al. 1977). Recent studies have demonstrated that Tau is concentrated on the labile domain of the axonal microtubules rather than on the stable domain, indicating that the role of Tau in the regulation of microtubule stability in the axon is not to stabilize axonal microtubules but to enable them to extend their labile domains (Baas and Qiang 2019). In addition to polymerizing microtubules and regulating their stability and mobility, Tau can regulate axonal transport. High concentrations of Tau bind to microtubules and differentially inhibit both dynein and kinesin functions, which are related to retrograde and anterograde transport of molecules in neurons, respectively (Dixit et al. 2008). However, Tau does not influence axonal transport within the physiological range (Tapia-Rojas et al. 2019), and studies have demonstrated that alterations in axonal transport can be observed only after Tau overexpression (Dubey et al. 2008). Thus, we can speculate that Tau influences axonal transport only under some pathological conditions.
In recent years, Tau has also been found in other subcellular structures and to exert different functions in these structures. First, nuclear Tau in its dephosphorylated state can protect DNA from damage, whereas Tau phosphorylation increases nuclear invagination and disrupts nucleocytoplasmic transport (Violet et al. 2014). One study demonstrated that hyperphosphorylated Tau interacts with components of the nuclear pore complex (NPC) to impair nucleocytoplasmic transport (Tripathi et al. 2019). Research on Tau-transgenic Drosophila showed that polyadenylated RNAs accumulate within and adjacent to Tau-induced nuclear envelope invaginations, leading to cell death (Cornelison et al. 2019). Paonessa et al. demonstrated that mutations in the MAPT gene result in microtubule-mediated deformation of the nucleus and disrupted nucleocytoplasmic transport (Paonessa et al. 2019). Second, under physiological conditions, low levels of Tau can be found at dendritic spines, where it regulates synaptic function in the dendritic/postsynaptic compartment (Frandemiche et al. 2014; Ittner et al. 2010). It is reported that Tau trans-locates to excitatory synapses in cultured mouse neurons and acute hippocampal slices, indicating that Tau might be involved in the regulation of synaptic plasticity (Frandemiche et al. 2014). Another study found that Tau participates in the postsynaptic targeting of the Src kinase Fyn. Additionally, knockout of Tau in mouse induces signal transduction disorder (Ittner et al. 2010).
Comprehensive investigations have revealed a role of Tau in physiology and pathology. Speculations on how Tau participate in or influence the pathophysiology of PD include the following: axonal transport dysfunction may contribute to the deposition of α-Syn and disable of excretion of metabolites (Dixit et al. 2008; Y. Wang and Mandelkow 2016); Tau translocation to the excitatory synapses may be involved in excitotoxicity in PD pathology (Frandemiche et al. 2014). Clarifying the association between Tau protein and PD is of interest, and additional research is warranted to explore possible mechanisms underlying PD.
Association between MAPT Gene and PD
As the popularity of GWAS technology has grown, numerous studies have been performed to explore risk loci for PD (Edwards et al. 2010; International Parkinson’s Disease Genomics Consortium et al. 2017; International Parkinson’s Disease Genomics Consortium (IPDGC) et al. 2014). Thus far, at least 41 risk loci have been identified to be associated with PD (International Parkinson’s Disease Genomics Consortium et al. 2017), among which, MAPT is one of the most studied risk genes. Two extended haplotypes, H1 and H2, differ in orientation and do not recombine, covering the entire MAPT gene (Hutton 2000; Pastor et al. 2002; Stefansson et al. 2005). Variants in MAPT can increase the risk of PD and influence the progression and clinical manifestations of the disease. A full sequencing and haplotype analysis of MAPT in PD showed that the H1 haplotype is associated with an increased risk of PD but that the H2 haplotype has protective effects (Li et al. 2018). The pathologic effects of the H1 haplotype seem to vary in different populations. For example, the results of GWAS in Europe and America show a significant association (Mata et al. 2011; Refenes et al. 2009; Trotta et al. 2012; International Parkinson´s disease consortium 2011; Rhodes et al. 2010; Kalinderi et al. 2011). In contrast, the results of studies in Asia are not consistent (Chen et al. 2016; Li et al. 2018; Satake et al. 2009). Such a lack of consensus in investigations among different populations likely stems from the effects of population structure and population-specific environmental interactions, and the different results of studies in Asia may be caused by clinical heterogeneity and variable reliability in methodological issues. Hence, more studies are needed to explore the influences of MAPT on PD onset in the Asian population.
In addition to the influence on disease susceptibility, variations in MAPT also contribute to the clinical heterogeneity of PD. Some studies have discovered that MAPT is an independent risk factor for the development of cognitive impairment or dementia in PD patients (Setó-Salvia et al. 2011; Williams-Gray et al. 2009). Other studies found that the MAPT gene is also associated with the severity of motor symptoms (Huang et al. 2011; G. Wang et al. 2016). In a 5-year follow-up study, the MAPT H1/H1 genotype was proven to be an independent predictor of dementia risk in PD patients (Williams-Gray et al. 2009). Compta et al. reported that MAPT rs242557 is associated with high CSF Tau levels and low Aβ levels in PD patients (Compta et al. 2011a, b). Another gene-based and pathway-enrichment analysis suggested that MAPT is involved in the development of olfactory dysfunction, one of the most common nonmotor symptoms of PD, in older individuals (Dong et al. 2015). Genetic evidence suggests that the MAPT gene participates in disease onset and contributes to the diverse clinical manifestations of PD. Thus, identifying MAPT genotypes may help to identify groups at high risk for the development of PD and provide the possibility for early preventive measures. Furthermore, the implications of MAPT on PD indicate that Tau may have an essential role in the pathophysiology of PD.
Post-mortem Observation of Tau in the PD Brain
In addition to α-Syn deposition, which is the characteristic pathology of PD, many studies have documented the occurrence of comorbid Tau in autopsy-confirmed PD brains (Table 1). Arima et al. found colocalization of Tau and α-Syn in LBs in PD as well as dementia with Lewy body (DLB) patients. They also classified the morphology of those inclusions into four types: (1) LBs with ring-shaped Tau immunoreactivity, (2) LBs surrounded by neurofibrillary tangles (NFTs), (3) α-Syn- and Tau-immunoreactive filamentous and granular masses, and (4) α-Syn- and Tau-immunoreactive dystrophic neurites (Arima et al. 1999). Another study excluded nonspecific antibody cross-reactivity by using a panel of monoclonal antibodies against Tau epitopes that span the entire length of the protein. The study showed colocalization of Tau and α-Syn in LBs, and most Tau-immunoreactive LBs were found in neurons vulnerable to NFTs, such as the locus coeruleus and basal nucleus of Meynert (Ishizawa et al. 2003). Galloway et al. found that an antibody specific for Tau does not react with LBs in the substantia nigra of isolated PD patients but can stain both the cortex and substantia nigra of dementia with Lewy bodies (DLB) patients (P G Galloway et al. 1988; Pamela G. Galloway et al. 1989). The discrepancy of these results may result from the variable reliability in the methodology applied.
Cell replacement has been explored as a therapeutic strategy to treat PD. In addition to the postmortem observation that Tau is deposited in PD patients’ brains, Tau pathology has been observed in healthy grafts transplanted to PD patients. Cisbani and colleagues detected hyperphosphorylated Tau in grafted tissue of two PD patients at 18 months and 16 years posttransplantation, respectively. They also found Tau-positive inclusions, neurofibrillary tangles, and neuropil threads in patients who underwent autopsy at 16 years posttransplantation (Cisbani et al. 2017). Another case report showed frequent neuronal perikaryal inclusions positive for both phosphorylated α-Syn and Tau in the graft of a 70-year-old man who underwent cell transplantation 21 years prior (Ornelas et al. 2020). It is speculated that pathological α-Syn and Tau can spread from the host to the graft in a cell-to-cell manner. However, the transplantation process may also make the graft more susceptible to the spontaneous generation of pathology or factors within the host environment. These Tau pathologies observed in PD patients remind us that Tau may participate in PD pathophysiology by interacting with α-Syn or LBs. Overall, the different morphologies of Tau and α-Syn colocalization detected by immunohistochemistry technology indicate that more than one mechanism is involved (Arima et al. 1999, 2000).
CSF Tau as a Biomarker for PD
PD can be subcategorized into different clinical subtypes based on etiology and clinical manifestations (Reich and Savitt 2019). Extensive investigations have attempted to develop biomarkers for the early and precise diagnosis of PD (Maass et al. 2019). Although many studies have shown that CSF α-Syn levels are lower in PD patients, a lack of association with the severity of disease and considerable overlap of values between control and diseased groups hamper the use of CSF α-Syn as a diagnostic marker (Delenclos et al. 2016; Maass et al. 2019). Hence, biomarkers that are more sensitive and specific are urgently needed to facilitate early and precise diagnosis and to track progression of the disease. Many investigations have explored the association between CSF Tau levels and the risk of developing PD or its clinical manifestations. Please see Table 2 for an overview of the literature.
CSF Tau levels are significantly associated with cognitive impairments in PD patients. Several meta-analyses have shown that PD patients with cognitive impairment have elevated total Tau (t-Tau) and phosphorylated Tau (p-Tau) and reduced Aβ42 levels compared with those without cognitive impairment (Buongiorno et al. 2011; W. T. Hu et al. 2010; X. Hu et al. 2017). Leverenz et al. observed a significant association between CSF Aβ42, Aβ42/t-Tau, and BDNF levels and cognitive impairment in PD patients without dementia (Leverenz et al. 2011). Further studies showed that CSF p-Tau and p-Tau/Aβ42 levels could predict cognitive decline in PD patients (Liu et al. 2015; Schrag et al. 2017). Some studies have also suggested that the lifetime prevalence of cognitive impairment in PD is 80% (Aarsland et al. 2003; Buter 2008; Hely et al. 2008), making it very important to recognize PD patients who are more likely to develop cognitive impairment. Furthermore, CSF Tau levels may help in the differentiation of tremor-dominant PD (TDPD) and nontremor-dominant PD (NTPD). Indeed, it has been reported that t-Tau and Tau/Aβ42 levels are higher in NTPD patients than in TDPD patients and that Tau levels are closely related to motor symptoms in NTPD (Jellinger 2012; Přikrylová Vranová et al. 2012). Thus, CSF Tau levels may help in the diagnosis of PD subtypes and lay the foundation for developing personalized therapeutic strategies.
CSF Tau levels can also be used as a biomarker to track the progression of PD. In a longitudinal study of PD patients, the change rates of t-Tau and t-Tau/Aβ42 correlated with the Unified Parkinson Disease Rating Scale (UPDRS) total or motor score change rate (The Parkinson Study Group DATATOP Investigators et al. 2013). Another longitudinal study detected increased p-Tau and p-Tau/t-Tau and decreased t-Tau/Aβ42 in the CSF of PD patients in 12 years (Mollenhauer et al. 2017). Dolatshahi et al. found that p-Tau levels in CSF were low and rose significantly during the 1-year follow-up in the PD group (Dolatshahi et al. 2018). As CSF Tau has become an essential index for diagnosis of AD and other tauopathologies (Blennow and Zetterberg 2018; Takashima et al. 2019), clinical realities, such as manifestations, should be considered in differential diagnosis. However, its potential as a predicting factor of the course development and an indicator in PD’s typology should not be ignored.
Experimental Evidence Supporting the Role of Tau in PD Pathophysiology
Various studies have employed transgenic PD mouse lines in which Tau is manipulated, reduced, or eliminated to explore the potential molecular pathways through which Tau may contribute to the pathophysiology of PD (Beauchamp 2018; Lei et al. 2012; Singh et al. 2019; Wills et al. 2011). Nevertheless, no consistent conclusion can be drawn thus far. The differences in the results of those studies may be due to intermodel variability. Some studies have been performed to explore changes in Tau protein in PD models. Wills and coworkers found increased hyperphosphorylated Tau in the striatum of adult A53T α-synuclein transgenic mice that colocalized with α-Syn, which was aggregated and accumulated in inclusion bodies (Wills et al. 2011). Further studies have shown that overexpression or mutation of α-Syn may increase the phosphorylation of Tau by promoting expression of GSK-3β, a primary kinase known to phosphorylate Tau at multiple sites (Ga and Adamczyk 2014; Kalinderi et al. 2011). Bardai et al. reported that the leucine-rich repeat kinase 2 (LRRK2) protein and mutations in the gene encoding it are the most common causes of familial PD and promote Tau neurotoxicity through dysregulation of actin and mitochondrial dynamics (Bardai et al. 2018). These studies suggest that Tau and α-Syn can promote each other’s pathological changes to form a vicious cycle, ultimately promoting the occurrence and development of PD.
Many in vitro studies have demonstrated that Tau and α-Syn can interact and promote aggregation of the other (Giasson 2003). Dasari and colleagues found that Tau interacts with the C-terminus of α-Syn and promotes the formation of toxic aggregations with distinct molecular conformations (Dasari et al. 2019). However, the results of in vivo studies remain controversial. Some research indicates that Tau is detrimental during the development of PD. Clinton and coworkers generated a mouse model expressing both α-Syn, Tau, and Aβ by mating 3xTg-AD mice (Tg(APPSwe, TauP301L)1Lfa) with A53T α-Synuclein transgenic mice and found that coexpression of the three proteins accelerated cognitive decline (Clinton et al. 2010). Singh et al. found aberrant localization of Tau to postsynaptic spines, which contributed to postsynaptic deficits and cognitive impairment in TgA53T mice. Furthermore, removal of endogenous Tau in A53T α-Synuclein transgenic mice ameliorated postsynaptic deficits and cognitive dysfunction (Singh et al. 2019; Teravskis et al. 2018). These results suggest that reducing Tau in the PD brain may break the vicious cycle of the two proteins and alleviate the symptoms of PD. Regardless, Morris and colleague reduced Tau levels in two kinds of PD models and found that this reduction failed to prevent motor deficits (Morris et al. 2011).
It has been reported that Tau-knockout mice develop motor deficits and cognitive impairment; thus, they have been used as an age-dependent model of parkinsonism in some studies. One study showed that knockout of Tau induced the accumulation of iron in dopaminergic neurons in the substantia nigra by impairing APP-mediated iron export. The authors found that Tau-knockout mice developed Parkinsonism and dementia (Lei et al. 2012). Leah C et al. reported olfactory and motor deficits in 7- and 15-month-old Tau-KO mice. They also found accumulation of α-Syn and autophagic impairment in the olfactory bulb, striatum, and substantia nigra at 7 and 15 months of age, respectively (Beauchamp 2018). The movement disorders caused by Tau deletion may be due to the loss of its normal function. These observations suggest that more caution should be taken when targeting Tau for the treatment of PD.
Conclusions
Pathological and genetic evidence suggests that Tau plays an essential role in the pathogenesis of PD. However, the underlying molecular mechanisms remain unclear. Although a great deal of progress has been made in the field of PD, further studies are needed to develop methods for early and precise diagnosis as well as more efficient therapies. CSF Tau levels can help in PD diagnosis and monitoring disease progression. Moreover, crosstalk of Tau and α-Syn can induce loss of physiological function and axonal transport dysfunction, ultimately inducing the deposition of toxic fibrils and cell death. Overall, understanding the mechanisms by which Tau contributes to the pathophysiology of PD will be helpful for the treatment of PD in the future.
Abbreviations
- PD:
-
Parkinson's disease
- AD:
-
Alzheimer's disease
- PDND:
-
Parkinson’s disease nondemented
- PDD:
-
Parkinson’s disease-related dementia
- HC:
-
Healthy control
- PD-CIND:
-
PD and cognitive impairment, not dementia
- aMCI:
-
Amnestic mild cognitive impairment
- DLB:
-
Dementia with Lewy bodies
- TDPD:
-
Tremor-dominant Parkinson’s disease
- NTPD:
-
Non-tremor-dominant Parkinson’s disease
- FTD:
-
Frontotemporal dementia
- EDO-PD:
-
Early disease onset Parkinson’s disease
- CBS:
-
Corticalbasal syndrome
- CBD:
-
Corticalbasal disease
- PD-CN:
-
Parkinson’s disease cognitively normal
- PD-MCI:
-
Parkinson’s disease with mild cognitive impairment
- 24-OHC:
-
24S-Hydroxycholesterol
- UPDRS:
-
Unified Parkinson Disease Rating Scale
References
Aarsland D, Andersen K, Larsen JP, Lolk A, Kragh-Sørensen P (2003) Prevalence and characteristics of dementia in Parkinson disease. Arch Neurol 60(3):387–392. https://doi.org/10.1001/archneur.60.3.387
Afitska K, Fucikova A, Shvadchak VV, Yushchenko DA (2019) α-Synuclein aggregation at low concentrations. Biochimica et Biophysica Acta (BBA) Proteins and Proteomics 1867(7–8):701–709. https://doi.org/10.1016/j.bbapap.2019.05.003
Alves G, Bronnick K, Aarsland D, Blennow K, Zetterberg H, Ballard C et al (2010) CSF amyloid- and tau proteins, and cognitive performance, in early and untreated Parkinson’s Disease: The Norwegian ParkWest study. J Neurol Neurosurg Psychiatry 81(10):1080–1086. https://doi.org/10.1136/jnnp.2009.199950
Arima K, Hirai S, Sunohara N, Aoto K, Izumiyama Y, Ueda K et al (1999) Cellular co-localization of phosphorylated tau- and NACPra-synuclein-epitopes in Lewy bodies in sporadic Parkinson’s disease and in dementia with Lewy bodies. Brain Res 843(1–2):53–61. https://doi.org/10.1016/s0006-8993(99)01848-x
Arima K, Mizutani T, Alim MA, Tonozuka-Uehara H, Izumiyama Y, Hirai S, Uéda K (2000) NACP/α-synuclein and tau constitute two distinctive subsets of filaments in the same neuronal inclusions in brains from a family of parkinsonism and dementia with Lewy bodies: Double-immunolabeling fluorescence and electron microscopic studies. Acta Neuropathol 100(2):115–121. https://doi.org/10.1007/s004010050002
Ascherio A, Schwarzschild MA (2016) The epidemiology of Parkinson’s disease: Risk factors and prevention. The Lancet Neurology 15(12):1257–1272. https://doi.org/10.1016/S1474-4422(16)30230-7
Baas PW, Qiang L (2019) Tau: It’s Not What You Think. Trends Cell Biol 29(6):452–461. https://doi.org/10.1016/j.tcb.2019.02.007
Balestrino R, Schapira AHV (2020) Parkinson disease. Eur J Neurol 27(1):27–42. https://doi.org/10.1111/ene.14108
Bardai FH, Ordonez DG, Bailey RM, Hamm M, Lewis J, Feany MB (2018) Lrrk promotes tau neurotoxicity through dysregulation of actin and mitochondrial dynamics. PLoS Biol 16(12):e2006265. https://doi.org/10.1371/journal.pbio.2006265
Beauchamp LC (2018) Ablation of tau causes an olfactory deficit in a murine model of Parkinson’s disease. Acta Neuropathol Commun 6(1):57. https://doi.org/10.1186/s40478-018-0560-y
Bibl M, Esselmann H, Lewczuk P, Trenkwalder C, Otto M, Kornhuber J et al (2010) Combined analysis of CSF Tau, A β 42, A β 1–42% and A β 1–40 ox % in Alzheimer’s disease, dementia with Lewy bodies and Parkinson’s disease dementia. Int J Alzheimers Dis 2010:1–7. https://doi.org/10.4061/2010/761571
Björkhem I, Patra K, Boxer AL, Svenningsson P (2018) 24S-Hydroxycholesterol correlates with Tau and is increased in cerebrospinal fluid in Parkinson’s disease and corticobasal syndrome. Front Neurol 9:756. https://doi.org/10.3389/fneur.2018.00756
Blennow K, Zetterberg H (2018) Biomarkers for Alzheimer’s disease: Current status and prospects for the future. J Intern Med 284(6):643–663. https://doi.org/10.1111/joim.12816
Bose A, Beal MF (2016) Mitochondrial dysfunction in Parkinson’s disease. J Neurochem 139:216–231. https://doi.org/10.1111/jnc.13731
Braak H, Tredici KD, Rüb U, de Vos RAI, Jansen Steur ENH, Braak E (2003) Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging 24(2):197–211. https://doi.org/10.1016/S0197-4580(02)00065-9
Bras JM, Singleton A (2009) Genetic susceptibility in Parkinson’s disease. Biochimica et Biophysica Acta (BBA) - Mol Basis Dis 1792(7):597–603. https://doi.org/10.1016/j.bbadis.2008.11.008
Buongiorno M, Compta Y, Martí MJ (2011) Amyloid-β and τ biomarkers in Parkinson’s disease–dementia. J Neurol Sci 310(1–2):25–30. https://doi.org/10.1016/j.jns.2011.06.046
Burbulla LF, Song P, Mazzulli JR, Zampese E, Wong YC, Jeon S et al (2017) Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease. Science 357(6357):1255–1261. https://doi.org/10.1126/science.aam9080
Buter TC (2008) Dementia and survival in Parkinson disease. Neurology 70:1017–1022. https://doi.org/10.1212/01.wnl.0000306632.43729.24
Cenini G, Lloret A, Cascella R (2019) Oxidative stress in neurodegenerative diseases: From a mitochondrial point of view. Oxid Med Cell Longev 2019:1–18. https://doi.org/10.1155/2019/2105607
Chartier-Harlin MC, Kachergus J, Roumier C, Mouroux V, Douay X, Lincoln S et al (2004) α-synuclein locus duplication as a cause of familial Parkinson’s disease. Lancet 364(9440):1167–1169. https://doi.org/10.1016/S0140-6736(04)17103-1
Chaudhuri KR, Healy DG, Schapira AHV (2006) Non-motor symptoms of Parkinson’s disease: Diagnosis and management. Lancet Neurol 5(3):235–245. https://doi.org/10.1016/S1474-4422(06)70373-8
Chen Y, Cao B, Ou R, Chen X, Zhao B, Wei Q et al (2016) Association analysis of the GRN rs5848 and MAPT rs242557 polymorphisms in Parkinson’s disease and multiple system atrophy: A large-scale population-based study and meta-analysis. Int J Neurosci 126(10):947–954. https://doi.org/10.3109/00207454.2015.1086345
Cisbani G, Maxan A, Kordower JH, Planel E, Freeman TB, Cicchetti F (2017) Presence of tau pathology within foetal neural allografts in patients with Huntington’s and Parkinson’s disease. Brain 140(11):2982–2992. https://doi.org/10.1093/brain/awx255
Cleveland DW, Hwo SY, Kirschner MW (1977) Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin. J Mol Biol 116(2):207–225. https://doi.org/10.1016/0022-2836(77)90213-3
Clinton LK, Blurton-Jones M, Myczek K, Trojanowski JQ, LaFerla FM (2010) Synergistic interactions between A, Tau, and -synuclein: acceleration of neuropathology and cognitive decline. J Neurosci 30(21):7281–7289. https://doi.org/10.1523/JNEUROSCI.0490-10.2010
Compta Y, Parkkinen L, O’Sullivan SS, Vandrovcova J, Holton JL, Collins C et al (2011) Lewy- and Alzheimer-type pathologies in Parkinson’s disease dementia: Which is more important? Brain 134(5):1493–1505. https://doi.org/10.1093/brain/awr031
Compta Y, Ezquerra M, Muñoz E, Tolosa E, Valldeoriola F, Rios J et al (2011) High cerebrospinal tau levels are associated with the rs242557 tau gene variant and low cerebrospinal β-amyloid in Parkinson disease. Neurosci Lett 487(2):169–173. https://doi.org/10.1016/j.neulet.2010.10.015
Compta Y, Martí MJ, Ibarretxe-Bilbao N, Junqué C, Tolosa E(2009) Cerebrospinal tau, phospho-tau, and beta-amyloid and neuropsychological functions in Parkinson’s disease. Mov Disord 24(15):2203–2210. https://doi.org/10.1002/mds.22594
Conway KA, Harper JD, Lansbury PT (1998) Accelerated in vitro fibril formation by a mutant α-synuclein linked to early-onset Parkinson disease. Nat Med 4(11):1318–1320. https://doi.org/10.1038/3311
Cornelison GL, Levy SA, Jenson T, Frost B (2019) Tau-induced nuclear envelope invagination causes a toxic accumulation of mRNA in Drosophila. Aging Cell 18(1):e12847. https://doi.org/10.1111/acel.12847
Cuervo AM (2004) Impaired degradation of mutant-synuclein by chaperone-mediated autophagy. Science 305(5688):1292–1295. https://doi.org/10.1126/science.1101738
Dasari AKR, Kayed R, Wi S, Lim KH (2019) Tau interacts with the C-terminal region of α-Synuclein, promoting formation of toxic aggregates with distinct molecular conformations. Biochem 58(25):2814–2821. https://doi.org/10.1021/acs.biochem.9b00215
Delenclos M, Jones DR, McLean PJ, Uitti RJ (2016) Biomarkers in Parkinson’s disease: advances and strategies. Parkinsonism Relat Disord 22:S106–S110. https://doi.org/10.1016/j.parkreldis.2015.09.048
Delgado-Alvarado M (2017) Tau/a-Synuclein ratio and inflammatory proteins in Parkinson’s disease: an exploratory study. Mov Disord 32(7):1066–1073. https://doi.org/10.1002/mds.27001
Delgado-Alvarado M, Dacosta-Aguayo R, Navalpotro-Gómez I, Gago B, Gorostidi A, Jiménez-Urbieta H et al (2018) Ratios of proteins in cerebrospinal fluid in Parkinson’s disease cognitive decline: Prospective study: CSF protein ratios and dementia in PD. Mov Disord 33(11):1809–1813. https://doi.org/10.1002/mds.27518
Deng H, Wang P, Jankovic J (2018) The genetics of Parkinson disease. Ageing Res Rev 42:72–85. https://doi.org/10.1016/j.arr.2017.12.007
Desplats P, Lee HJ, Bae EJ, Patrick C, Rockenstein E, Crews L et al (2009) Inclusion formation and neuronal cell death through neuron-to-neuron transmission of -synuclein. Proc Natl Acad Sci 106(31):13010–13015. https://doi.org/10.1073/pnas.0903691106
Dixit R, Ross JL, Goldman YE, Holzbaur ELF (2008) Differential regulation of dynein and kinesin motor proteins by Tau. Science 319(5866):1086–1089. https://doi.org/10.1126/science.1152993
Dolatshahi M, Pourmirbabaei S, Kamalian A, Ashraf-Ganjouei A, Yaseri M, Aarabi MH (2018) Longitudinal alterations of alpha-Synuclein, amyloid beta, total, and phosphorylated Tau in cerebrospinal fluid and correlations between their changes in Parkinson’s disease. Front Neurol 9:560. https://doi.org/10.3389/fneur.2018.00560
Dong J, Yang J, Tranah G, Franceschini N, Parimi N, Alkorta-Aranburu G et al (2015) Genome-wide meta-analysis on the sense of smell among US older adults. Medicine 94(47):e1892. https://doi.org/10.1097/MD.0000000000001892
Dubey M, Chaudhury P, Kabiru H, Shea TB (2008) Tau inhibits anterograde axonal transport and perturbs stability in growing axonal neurites in part by displacing kinesin cargo: Neurofilaments attenuate tau-mediated neurite instability. Cell Motil Cytoskelet 65(2):89–99. https://doi.org/10.1002/cm.20243
Edwards TL, Scott WK, Almonte C, Burt A, Powell EH, Beecham GW et al (2010) Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann Hum Genet 74(2):97–109. https://doi.org/10.1111/j.1469-1809.2009.00560.x
Fereshtehnejad S-M, Zeighami Y, Dagher A, Postuma RB (2017) Clinical criteria for subtyping Parkinson’s disease: Biomarkers and longitudinal progression. Brain 140(7):1959–1976. https://doi.org/10.1093/brain/awx118
Frandemiche ML, Seranno SD, Rush T, Borel E, Elie A, Arnal I et al (2014) Activity-dependent Tau protein translocation to excitatory synapse is disrupted by exposure to amyloid-beta oligomers. J Neurosci 34(17):6084–6097. https://doi.org/10.1523/JNEUROSCI.4261-13.2014
Ga M, Adamczyk A (2014) Extracellular a-Synuclein leads to microtubule destabilization via GSK-3b-dependent Tau phosphorylation in PC12 cells. PLoS ONE 9(4):11
Galloway PG, Grundke-Iqbal I, Iqbal K, Perry G (1988) Lewy bodies contain epitopes both shared and distinct from Alzheimer neurofibrillary tangles. J Neuropathol Exp Neurol 47(6):654–663. https://doi.org/10.1097/00005072-198811000-00008
Galloway PG, Bergeron C, Perry G (1989) The presence of tau distinguishes Lewy bodies of diffuse Lewy body disease from those of idiopathic Parkinson disease. Neurosci Lett 100(1–3):6–10. https://doi.org/10.1016/0304-3940(89)90651-4
Ghosh D, Mehra S, Sahay S, Singh PK, Maji SK (2017) α-synuclein aggregation and its modulation. Int J Biol Macromol 100:37–54. https://doi.org/10.1016/j.ijbiomac.2016.10.021
Giasson BI (2003) Initiation and synergistic fibrillization of Tau and alpha-synuclein. Science 300(5619):636–640. https://doi.org/10.1126/science.1082324
Gmitterová K (2018) Cerebrospinal fluid markers analysis in the differential diagnosis of dementia with Lewy bodies and Parkinson’s disease dementia. Eur Arch Psychiatry Clin Neurosci 270(4):461–470. https://doi.org/10.1007/s00406-018-0928-9
Goedert M, Spillantini MC, Rutherford D, Crowther RA (1989) Multiple lsoforms of human microtubule-associated protein Tau: Sequences and localization in neurofibrillah tangles of Alzheimer’s disease. Neuron 3(4):519–526. https://doi.org/10.1016/0896-6273(89)90210-9
Grassi D, Howard S, Zhou M, Diaz-Perez N, Urban NT, Guerrero-Given D et al (2018) Identification of a highly neurotoxic α-synuclein species inducing mitochondrial damage and mitophagy in Parkinson’s disease. Proc Natl Acad Sci 115(11):E2634–E2643. https://doi.org/10.1073/pnas.1713849115
Hacker ML, Turchan M, Heusinkveld LE, Currie AD, Millan SH, Molinari AL et al (2020) Deep brain stimulation in early-stage Parkinson’s disease: five year outcomes. Neurology 95(4):e393–e401. https://doi.org/10.1212/WNL.0000000000009946
Hansen AK, Parbo P, Ismail R, Østergaard K, Brooks DJ, Borghammer P (2020) Tau rangles in Parkinson’s disease: A 2-year follow-up flortaucipir PET study. J Parkinsons Dis 10(1):161–171. https://doi.org/10.3233/JPD-191774
Hayes MT (2019) Parkinson’s disease and Parkinsonism. Am J Med 132(7):802–807. https://doi.org/10.1016/j.amjmed.2019.03.001
Hely MA, Reid WGJ, Adena MA, Halliday GM, Morris JGL (2008) The Sydney multicenter study of Parkinson’s disease: The inevitability of dementia at 20 years: Twenty Year Sydney Parkinson’s Study. Mov Disord 23(6):837–844. https://doi.org/10.1002/mds.21956
Hemmati-Dinarvand M, Saedi S, Valilo M, Kalantary-Charvadeh A, Alizadeh Sani M, Kargar R et al (2019) Oxidative stress and Parkinson’s disease: Conflict of oxidant-antioxidant systems. Neurosci Lett 709:134296. https://doi.org/10.1016/j.neulet.2019.134296
Himmelberg MM, West RJH, Elliott CJH, Wade AR (2018) Abnormal visual gain control and excitotoxicity in early-onset Parkinson’s disease Drosophila models. J Neurophysiol 119(3):957–970. https://doi.org/10.1152/jn.00681.2017
Hu WT, Chen-Plotkin A, Arnold SE, Grossman M, Clark CM, Shaw LM et al (2010) Biomarker discovery for Alzheimer’s disease, frontotemporal lobar degeneration, and Parkinson’s disease. Acta Neuropathol 120(3):385–399. https://doi.org/10.1007/s00401-010-0723-9
Hu X, Yang Y, Gong D (2017) Changes of cerebrospinal fluid Aβ42, t-tau, and p-tau in Parkinson’s disease patients with cognitive impairment relative to those with normal cognition: A meta-analysis. Neurol Sci 38(11):1953–1961. https://doi.org/10.1007/s10072-017-3088-1
Huang Y, Rowe DB, Halliday GM (2011) Interaction between α-Synuclein and Tau genotypes and the progression of Parkinson’s disease. J Parkinsons Dis 1(3):271–276. https://doi.org/10.3233/JPD-2011-11027
Hutton M (2000) Molecular genetics of chromosome 17 Tauopathies 920:63–73. https://doi.org/10.1111/j.1749-6632.2000.tb06906.x
International Parkinson Disease Genomics Consortium, Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM et al (2011) Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet 377(9766):641–649. https://doi.org/10.1016/S0140-6736(10)62345-8
International Parkinson’s Disease Genomics Consortium, 23 and Me Research Team, Chang D, Nalls MA, Hallgrímsdóttir IB, Hunkapiller J et al (2017) A meta-analysis of genome-wide association studies identifies 17 new Parkinson’s disease risk loci. Nat Gen 49(10):1511–1516. https://doi.org/10.1038/ng.3955
International Parkinson’s Disease Genomics Consortium (IPDGC), Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI), 23andMe, GenePD, NeuroGenetics Research Consortium (NGRC), Hussman Institute of Human Genomics (HIHG) et al (2014) Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease. Nat Gen 46(9):989–993. https://doi.org/10.1038/ng.3043
Ishizawa T, Mattila P, Davies P, Wang D, Dickson DW (2003) Colocalization of Tau and alpha-Synuclein epitopes in Lewy bodies. J Neuropathol Exp Neurol 62(4):389–397. https://doi.org/10.1093/jnen/62.4.389
Ittner LM, Ke YD, Delerue F, Bi M, Gladbach A, van Eersel J et al (2010) Dendritic function of Tau mediates amyloid-β toxicity in Alzheimer’s disease mouse models. Cell 142(3):387–397. https://doi.org/10.1016/j.cell.2010.06.036
Jamwal S, Kumar P (2019) Insight into the emerging role of striatal neurotransmitters in the pathophysiology of Parkinson’s disease and Huntington’s disease: A review. Curr Neuropharmacol 17(2):165–175. https://doi.org/10.2174/1570159X16666180302115032
Jellinger KA (2012) CSF biomarkers in different phenotypes of Parkinson disease. J Neural Trans 119(4):455–456. https://doi.org/10.1007/s00702-011-0736-0
Kalinderi K, Fidani L, Katsarou Z, Clarimón J, Bostantjopoulou S, Kotsis A (2011) GSK3β polymorphisms, MAPT H1 haplotype and Parkinson’s disease in a Greek cohort. Neurobiol Aging 32(3):546.e1-546.e5. https://doi.org/10.1016/j.neurobiolaging.2009.05.007
Kaur R, Mehan S, Singh S (2019) Understanding multifactorial architecture of Parkinson’s disease: pathophysiology to management. Neurol Sci 40(1):13–23. https://doi.org/10.1007/s10072-018-3585-x
Krack P, Batir A, Van Blercom N, Chabardes S, Fraix V, Ardouin C et al (2003) Five-year follow-up of bilateral stimulation of the subthalamic nucleus in advanced Parkinson’s disease. N Engl J Med 349(20):1925–1934. https://doi.org/10.1056/NEJMoa035275
Lee Gl, Cowan N, Kirschner M (1988) The primary structure and heterogeneity of Tau protein from mouse brain. Science 239(4837):285–288. https://doi.org/10.1126/science.3122323
Lei P, Ayton S, Finkelstein DI, Spoerri L, Ciccotosto GD, Wright DK et al (2012) Tau deficiency induces parkinsonism with dementia by impairing APP-mediated iron export. Nat Med 18(2):291–295. https://doi.org/10.1038/nm.2613
Lerche S, Wurster I, Röben B, Machetanz G, Zimmermann M, Bernhard F et al (2019) Parkinson’s disease: Evolution of cognitive impairment and CSF Aβ 1–42 profiles in a prospective longitudinal study. J Neurol Neurosurg Psychiatry 90(2):165–170. https://doi.org/10.1136/jnnp-2018-318956
Leverenz JB, Stennis Watson G, Shofer J, Zabetian CP, Zhang J, Montine TJ (2011) Cerebrospinal fluid biomarkers and cognitive performance in non-demented patients with Parkinson’s disease. Parkinsonism Relat Disor 17(1):61–64. https://doi.org/10.1016/j.parkreldis.2010.10.003
Li J, Ruskey JA, Arnulf I, Dauvilliers Y, Hu MTM, Högl B et al (2018) Full sequencing and haplotype analysis of MAPT in Parkinson’s disease and rapid eye movement sleep behavior disorder: MAPT in PD and RBD. Mov Disord 33(6):1016–1020. https://doi.org/10.1002/mds.27385
Liu C, Cholerton B, Shi M, Ginghina C, Cain KC, Auinger P, Zhang J (2015) CSF tau and tau/Aβ42 predict cognitive decline in Parkinson’s disease. Parkinsonism Relat Disor 21(3):271–276. https://doi.org/10.1016/j.parkreldis.2014.12.027
Maass F, Schulz I, Lingor P, Mollenhauer B, Bähr M (2019) Cerebrospinal fluid biomarker for Parkinson’s disease: An overview. Mol Cell Neurosci 97:60–66. https://doi.org/10.1016/j.mcn.2018.12.005
Mata IF, Yearout D, Alvarez V, Coto E, de Mena L, Ribacoba R et al (2011) Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson’s disease. Mov Disord 26(5):819–823. https://doi.org/10.1002/mds.23642
McNaught KSP, Björklund LM, Belizaire R, Isacson O, Jenner P, Olanow CW (2002) Proteasome inhibition causes nigral degeneration with inclusion bodies in rats: Neuroreport 13(11):1437–1441. https://doi.org/10.1097/00001756-200208070-00018
Mehra S, Sahay S, Maji SK (2019) α-Synuclein misfolding and aggregation: Implications in Parkinson’s disease pathogenesis. Biochimica et Biophysica Acta (BBA) - Proteins Proteom 1867(10):890–908. https://doi.org/10.1016/j.bbapap.2019.03.001
Mietelska-Porowska A, Wasik U, Goras M, Filipek A, Niewiadomska G (2014) Tau protein modifications and interactions: their role in function and dysfunction. Int J Mol Sci 15(3):4671–4713. https://doi.org/10.3390/ijms15034671
Mollenhauer B, Caspell-Garcia CJ, Coffey CS, Taylor P, Shaw LM, Trojanowski JQ et al (2017) Longitudinal CSF biomarkers in patients with early Parkinson disease and healthy controls. Neurol 89(19):1959–1969. https://doi.org/10.1212/WNL.0000000000004609
Montine TJ, Shi M, Quinn JF, Peskind ER, Craft S, Ginghina C et al (2010) CSF Aβ 42 and tau in Parkinson’s disease with cognitive impairment: CSF biomarkers for PD with CI or dementia. Mov Disord 25(15):2682–2685. https://doi.org/10.1002/mds.23287
Morris M, Koyama A, Masliah E, Mucke L (2011) Tau reduction does not prevent motor deficits in two mouse models of Parkinson’s disease. PLoS ONE 6(12):e29257. https://doi.org/10.1371/journal.pone.0029257
Nguyen M, Wong YC, Ysselstein D, Severino A, Krainc D (2019) Synaptic, mitochondrial, and lysosomal dysfunction in Parkinson’s disease. Trends Neurosci 42(2):140–149. https://doi.org/10.1016/j.tins.2018.11.001
Ornelas AS, Adler CH, Serrano GE, Curry JR, Shill HA, Kopyov O, Beach TG (2020) Co-Existence of tau and α-synuclein pathology in fetal graft tissue at autopsy: A case report. Parkinsonism Relat Disor 71:36–39. https://doi.org/10.1016/j.parkreldis.2019.12.013
Paonessa F, Evans LD, Solanki R, Larrieu D, Wray S, Hardy J et al (2019) Microtubules deform the nuclear membrane and disrupt nucleocytoplasmic transport in tau-mediated frontotemporal dementia. Cell Rep 26(3):582-593.e5. https://doi.org/10.1016/j.celrep.2018.12.085
Parnetti L, Chiasserini D, Bellomo G, Giannandrea D, De Carlo C, Qureshi MM et al (2011) Cerebrospinal fluid Tau/α-synuclein ratio in Parkinson’s disease and degenerative dementias. Mov Disord 26(8):1428–1435. https://doi.org/10.1002/mds.23670
Parnetti L, Farotti L, Eusebi P, Chiasserini D, De Carlo C, Giannandrea D et al (2014) Differential role of CSF alpha-synuclein species, tau, and Aβ42 in Parkinson’s disease. Front Aging Neurosci 6:53. https://doi.org/10.3389/fnagi.2014.00053
Pastor P, Ezquerra M, Tolosa E, Muñoz E, José Martí M, Valldeoriola F et al (2002) Further extension of the H1 haplotype associated with progressive supranuclear palsy: Extension of the H1 Haplotype Associated with PSP. Mov Disord 17(3):550–556. https://doi.org/10.1002/mds.10076
Přikrylová Vranová H, Mareš J, Hluštík P, Nevrlý M, Stejskal D, Zapletalová J et al (2012) Tau protein and beta-amyloid1-42 CSF levels in different phenotypes of Parkinson’s disease. J Neural Transm 119(3):353–362. https://doi.org/10.1007/s00702-011-0708-4
Přikrylová Vranová H, Mareš J, Nevrlý M, Stejskal D, Zapletalová J, Hluštík P, Kaňovský P (2010) CSF markers of neurodegeneration in Parkinson’s disease. J Neural Transm 117(10):1177–1181. https://doi.org/10.1007/s00702-010-0462-z
Refenes N, Bolbrinker J, Tagaris G, Orlacchio A, Drakoulis N, Kreutz R (2009) Role of the H1 haplotype of microtubule-associated protein tau (MAPT) gene in Greek patients with Parkinson’s disease. BMC Neurol 9(1):26. https://doi.org/10.1186/1471-2377-9-26
Reich SG, Savitt JM (2019) Parkinson’s disease. Med Clin North Am 103(2):337–350. https://doi.org/10.1016/j.mcna.2018.10.014
Rhodes SL, Sinsheimer JS, Bordelon Y, Bronstein JM, Ritz B (2010) Replication of GWAS associations for GAK and MAPT in Parkinson’s disease: Replication of GAK and MAPT associations in PD. Ann Hum Genet 75(2):195–200. https://doi.org/10.1111/j.1469-1809.2010.00616.x
Ross OA, Braithwaite AT, Skipper LM, Kachergus J, Hulihan MM, Middleton FA et al (2008) Genomic investigation of α-synuclein multiplication and parkinsonism. Ann Neurol 63(6):743–750. https://doi.org/10.1002/ana.21380
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M et al (2009) Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson’s disease. Nat Genet 41(12):1303–1307. https://doi.org/10.1038/ng.485
Schrag A, Siddiqui UF, Anastasiou Z, Weintraub D, Schott JM (2017) Clinical variables and biomarkers in prediction of cognitive impairment in patients with newly diagnosed Parkinson’s disease: A cohort study. Lancet Neurol 16(1):66–75. https://doi.org/10.1016/S1474-4422(16)30328-3
Setó-Salvia N, Clarimón J, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Combarros O et al (2011) Dementia risk in Parkinson disease: Disentangling the role of MAPT haplotypes. Arch Neurol 68(3):359–364. https://doi.org/10.1001/archneurol.2011.17
Shi M, Kovac A, Korff A, Cook TJ, Ginghina C, Bullock KM et al (2016) CNS tau efflux via exosomes is likely increased in Parkinson’s disease but not in Alzheimer’s disease. Alzheimers Dement 12(11):1125–1131. https://doi.org/10.1016/j.jalz.2016.04.003
Singh B, Covelo A, Martell-Martínez H, Nanclares C, Sherman MA, Okematti E et al (2019) Tau is required for progressive synaptic and memory deficits in a transgenic mouse model of α-synucleinopathy. Acta Neuropathol 138(4):551–574. https://doi.org/10.1007/s00401-019-02032-w
Stefansson H, Helgason A, Thorleifsson G, Steinthorsdottir V, Masson G, Barnard J et al (2005) A common inversion under selection in Europeans. Nat Genet 37(2):129–137. https://doi.org/10.1038/ng1508
Subramaniam SR, Chesselet M-F (2013) Mitochondrial dysfunction and oxidative stress in Parkinson’s disease. Prog Neurobiol 106–107:17–32. https://doi.org/10.1016/j.pneurobio.2013.04.004
Sveinbjornsdottir S (2016) The clinical symptoms of Parkinson’s disease. J Neurochem 139:318–324. https://doi.org/10.1111/jnc.13691
Takashima A, Wolozin B, Buee L (Eds.) (2019) Tau Biology (Vol. 1184) Singapore: Springer Singapore. https://doi.org/10.1007/978-981-32-9358-8
Tapia-Rojas C, Cabezas-Opazo F, Deaton CA, Vergara EH, Johnson GVW, Quintanilla RA (2019) It’s all about tau. Prog Neurobiol 175:54–76. https://doi.org/10.1016/j.pneurobio.2018.12.005
Teravskis PJ, Covelo A, Miller EC, Singh B, Martell-Martínez HA, Benneyworth MA et al (2018) A53T mutant alpha-synuclein induces Tau-dependent postsynaptic impairment independently of neurodegenerative changes. J Neurosci 38(45):9754–9767. https://doi.org/10.1523/JNEUROSCI.0344-18.2018
The Parkinson Study Group DATATOP Investigators, Zhang J, Mattison HA, Liu C, Ginghina, C, Auinger, P et al (2013) Longitudinal assessment of tau and amyloid beta in cerebrospinal fluid of Parkinson disease Acta Neuropathol 126(5):671–682. https://doi.org/10.1007/s00401-013-1121-x
Tripathi T, Prakash J, Shav-Tal Y (2019) Phospho-Tau impairs nuclear-cytoplasmic transport. ACS Chemical Neuroscience 10(1):36–38. https://doi.org/10.1021/acschemneuro.8b00632
Trotta L, Guella I, Soldà G, Sironi F, Tesei S, Canesi M et al (2012) SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population. Parkinsonism Relat Disor 18(3):257–262. https://doi.org/10.1016/j.parkreldis.2011.10.014
Vasili E, Dominguez-Meijide A, Outeiro TF (2019) Spreading of α-Synuclein and Tau: A systematic comparison of the mechanisms involved. Front Mol Biosci 12:107. https://doi.org/10.3389/fnmol.2019.00107
Violet M, Delattre L, Tardivel M, Sultan A, Chauderlier A, Caillierez R et al (2014) A major role for Tau in neuronal DNA and RNA protection in vivo under physiological and hyperthermic conditions. Front Cell Neurosci 8:84. https://doi.org/10.3389/fncel.2014.00084
Wakabayashi K, Tanji K, Odagiri S, Miki Y, Mori F, Takahashi H (2013) The Lewy body in Parkinson’s disease and related neurodegenerative disorders. Mol Neurobiol 47(2):495–508. https://doi.org/10.1007/s12035-012-8280-y
Wang G, Huang Y, Chen W, Chen S, Wang Y, Xiao Q et al (2016) Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson’s disease. Parkinsonism Relat Disor 24:89–94. https://doi.org/10.1016/j.parkreldis.2015.12.018
Wang Y, Mandelkow E (2016) Tau in physiology and pathology. Nat Rev Neurosci 17(1):22–35. https://doi.org/10.1038/nrn.2015.1
Williams-Gray CH, Evans JR, Goris A, Foltynie T, Ban M, Robbins TW et al (2009) The distinct cognitive syndromes of Parkinson’s disease: 5 year follow-up of the CamPaIGN cohort. Brain 132(11):2958–2969. https://doi.org/10.1093/brain/awp245
Wills J, Credle J, Haggerty T, Lee J-H, Oaks AW, Sidhu A (2011) Tauopathic changes in the striatum of A53T α-Synuclein mutant mouse model of Parkinson’s disease. PLoS ONE 6(3):e17953. https://doi.org/10.1371/journal.pone.0017953
Winer JR, Maass A, Pressman P, Stiver J, Schonhaut DR, Baker SL et al (2018) Associations between Tau, β-amyloid, and cognition in Parkinson disease. JAMA Neurology 75(2):227. https://doi.org/10.1001/jamaneurol.2017.3713
Yamada K, Iwatsubo T (2018) Extracellular α-synuclein levels are regulated by neuronal activity. Mol Neurodegener 13(1):9. https://doi.org/10.1186/s13024-018-0241-0
Funding
This work was supported by grants from the National Nature Science Foundation of China (Nos. 81822016, 81771382, and 81571249 to Z. Zhang and No. 81901291 to M. He).
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Lanxia Meng, Mingyang He, and Zhentao Zhang conceived the project. Lina Pan performed the literature review and wrote the manuscript. Zhentao Zhang supervised the work and edited the final version.
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Pan, L., Meng, L., He, M. et al. Tau in the Pathophysiology of Parkinson’s Disease. J Mol Neurosci 71, 2179–2191 (2021). https://doi.org/10.1007/s12031-020-01776-5
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DOI: https://doi.org/10.1007/s12031-020-01776-5