Abstract
Heart disease involves irreversible myocardial injury that leads to high morbidity and mortality rates. Numerous cell-based cardiac in vitro models have been proposed as complementary approaches to non-clinical animal research. However, most of these approaches struggle to accurately replicate adult human heart conditions, such as myocardial infarction and ventricular remodeling pathology. The intricate interplay between various cell types within the adult heart, including cardiomyocytes, fibroblasts, and endothelial cells, contributes to the complexity of most heart diseases. Consequently, the mechanisms behind heart disease induction cannot be attributed to a single-cell type. Thus, the use of multi-cellular models becomes essential for creating clinically relevant in vitro cell models. This study focuses on generating self-organizing heart organoids (HOs) using human-induced pluripotent stem cells (hiPSCs). These organoids consist of cardiomyocytes, fibroblasts, and endothelial cells, mimicking the cellular composition of the human heart. The multi-cellular composition of HOs was confirmed through various techniques, including immunohistochemistry, flow cytometry, q-PCR, and single-cell RNA sequencing. Subsequently, HOs were subjected to hypoxia-induced ischemia and ischemia-reperfusion (IR) injuries within controlled culture conditions. The resulting phenotypes resembled those of acute myocardial infarction (AMI), characterized by cardiac cell death, biomarker secretion, functional deficits, alterations in calcium ion handling, and changes in beating properties. Additionally, the HOs subjected to IR efficiently exhibited cardiac fibrosis, displaying collagen deposition, disrupted calcium ion handling, and electrophysiological anomalies that emulate heart disease. These findings hold significant implications for the advancement of in vivo-like 3D heart and disease modeling. These disease models present a promising alternative to animal experimentation for studying cardiac diseases, and they also serve as a platform for drug screening to identify potential therapeutic targets.
Similar content being viewed by others
Introduction
Organoids are distinctive three-dimensional (3D) cellular models, as they effectively recapitulate numerous aspects of the intricate structure and functionality observed in tissues, making them invaluable tools in biological and medical research [1].
Unlike other tissues, the heart has limited capacity for regeneration, and endomyocardial biopsies are difficult to obtain [2,3,4]. Consequently, many researchers have endeavored to generate 3D cardiac models from induced pluripotent stem cells (iPSCs) to facilitate in vitro cardiac studies [2, 5]. However, the most previously reported cardiac organoid (CO) models center on a 3D architecture constructed via the cardiac spheroid technique, which entails fusing iPSC-derived cardiomyocytes [6, 7].
Conversely, several studies have unveiled COs encompassing diverse cell populations. Drakhils et al., for instance, harnessed human iPSC aggregates embedded in matrigel to generate human heart-forming organoids, thereby recapitulating early human heart and foregut development [8]. Similarly, another research group generated iPSC-derived cardioids harboring key cardiac cell types [9, 10]. These cardioids exhibited the development of small and large cavities mirroring heart maturation [11]. However, while these cardiac models are suitable for studying early heart development, there remains a critical need for the development of more robust 3D cardiac models that faithfully mimic the intricate attributes of adult heart tissue with multi-cellular compositions.
CO models also have the potential to significantly advance studies related to human physiological functions of tissues and the pathological mechanisms underlying human diseases [12, 13]. These models address limitations posed by animal models and traditional 2D monolayer cell cultures, which fail to replicate certain aspects of human biology [14, 15]. In a recent study, localized cryoinjury induced extracellular matrix accumulation in COs [11, 16]. Another study involved culturing iPSC-derived COs with 10% O2 and 1 μM noradrenaline, creating an apoptosis gradient that emulates the myocardial infarction environment [17]. These reports shed light on molecular and cellular regulatory mechanisms governing the regenerative capacity of immature human hearts and establish an in vitro model for cardiovascular disease. Nonetheless, these organoids have struggled to comprehensively mimic adult human heart failure, encompassing the intricate mechanisms of the disease.
In this study, our focus was on developing multi-cellular heart organoids (HOs) from human iPSCs mirroring the proportional composition of the human adult heart. Subsequently, perturbation of cellular interactions in the HOs by defined culture conditions efficiently recapitulated the heart disease from initial responses following myocardial infarction to subsequent fibrotic activation in the HOs.
Materials and methods
hiPSCs culture and generation of COs and HOs
The hiPSCs were expanded and cultured under feeder-free conditions on Matrigel (Corning, USA) coated T75 tissue culture flasks in the presence of mTeSR1 (Stem Cell Technologies, Canada). Cardiac organoid (CO) differentiation was performed as described in our previous reports [18]. To differentiate heart organoids (HOs), we initially applied the differentiation procedures used for COs to induce mesodermal differentiation. However, the differentiated mesoderm was subsequently cultured with BMP, VEGF, FGF, and TGF-beta-containing medium from D8 to D14 to induce differentiation into multi-lineages. Following multi-lineage induction, the HOs were maintained in RPMI 1640 medium supplemented with 10 ng/ml of TGFβ and B-27 without vitamin A until day 30 (D30).
Further details on the induction of disease models and analysis were described in the supplementary information.
Results
Derivation of HOs from hiPSCs
We previously generated hiPSC-derived cardiac organoids (COs), and the CO formation resulted in the enhanced maturity of hiPSC-derived cardiomyocytes [18]. However, these COs could not mimic the diverse cellular composition of the human heart. Thus, we refined our differentiation protocol to generate heart organoids (HOs) designed to accommodate the coexistence of various cardiac lineage cells by modulating BMP, VEGF, FGF, and TGFβ signaling during differentiation (Fig. 1A).
An assessment of organoid beating efficiency spanned the entire differentiation period from day 8 to day 30 for both COs and HOs (Fig. 1B). On day 8–10 of differentiation, both COs and HOs initiated discernible beating (Fig. 1B). Notably, COs showed a beating efficiency of 68.1%, whereas HOs exhibited a lower rate of 34.5% on day 8 of differentiation. However, although the beating efficiency at the beginning of differentiation was higher in COs than in HOs, HOs displayed an ascending trend in their beating rate post-differentiation initiation, culminating in a 100% beating efficiency by day 30 (Fig. 1B), and resulted in similar beating efficiency to COs on day 30 (Fig. 1C, Videos 1 and 2).
Moreover, we validated the cardiomyocyte subtypes in the organoids by confirming the expression levels of MLC-2v and MLC-2a, indicative of ventricular and atrial types of cardiomyocytes, respectively. We observed that the expression of MLC-2a initiated early in differentiation (from D5 to D10), while MLC-2v expression gradually increased over the differentiation period. At D24, the majority of cardiomyocytes in both COs and HOs exhibited strong expression of MLC-2v (Fig. S1A and B).
Cellular compositions of HOs
To assess the cellular distribution in the COs and HOs, FACS analysis was performed (Figs. 2A, B and S2). Within COs, the mean distribution of cTnT, CD90, and VE-cadherin was 92.23 ± 2.62%, 6.24 ± 1.55%, and 4.73 ± 1.48%, respectively (Figs. 2A, B and S2). Conversely, in HOs, these distributions were determined to be 51.09 ± 5.92%, 24.63 ± 4.08%, and 14.03 ± 3.34%, respectively (Figs. 2A, B and S2).
Immunostaining was also performed to visualize the distribution of cardiac lineage cells (Fig. 2C and D). Consistently with FACS analysis, COs prominently displayed cTnT expression within the organoids, while HOs displayed VE-cadherin expression on the surface of HOs (Fig. 2C, Videos 3, 4). The distinct distribution of blood vessel cells in HOs was further verified through the culture of dissociated organoids, and the dissociated cells from HOs exhibited a composition of both cTnT-positive cells and VE-Cad-positive cells (Fig. 2C). In contrast, the dissociated cells from COs exclusively displayed cTnT-positive cells (Fig. 2C). In addition, the HOs exhibited notable expression of Vimentin, a fibroblast marker, in comparison to COs (Fig. 2D).
The differences were further validated through qPCR analysis, and this analysis substantiated that COs exhibited a relatively increased expression of NKX 2.5, a transcription factor governing heart development, in addition to TNNT2, MYL2, and MYL7 (Fig. 2E). In contrast, HOs displayed significant upregulation in genes related to cardiac fibroblasts (CD90 and PDGFRα), Vimentin, and TCF21, all in comparison to COs (Fig. 2E). Furthermore, endothelial-related genes including CD34, PECAM1, SOX17, and FOXA2 exhibited elevated expression levels in HOs relative to COs (Fig. 2E).
Single-cell transcriptomic analysis of HOs
To gain a deeper understanding of the intricate gene expression within HOs, we utilized single-cell RNA sequencing (Fig. 3). Utilizing UMAP clustering and marker identification, the pool of 2587 cells from HOs was effectively categorized into distinct groups, encompassing cardiomyocytes, fibroblasts, and endothelial cells (Fig. 3A). To compare the representative gene expression patterns by cell type in both COs and HOs, we selected genes with p-values below 0.05 and visualized their expression using violin plots. Additionally, a comparative examination of gene expression patterns between COs and HOs was presented through violin plots. Notably, representative genes linked to cardiomyocytes, such as MYL2, MYL7, MYH7, TNNC1, MYBP3, and CACNA1C, exhibited enhanced expression in COs when compared to HOs (Fig. 3B). Similarly, an analysis was also extended to endothelial cells. Endothelial-related genes such as APOLD1, GIMAP4, PECAM1, PRSS23, STC1, and VEGFC exhibited an upregulation in HOs compared to COs (Fig. 3C). Shifting the focus to cardiac fibroblasts, the violin plots highlighted genes like AGT, CLU, and HMGA1 illustrating disparities between COs and HOs (Fig. 3D).
Clusters where unselected genes were grouped under the “unclassified” category in HOs were further analyzed (Fig. 3A). To predict cell types within the populations, we made use of databases such as pangiaoDB and GeneCard. These predictions revealed that the unclassified population mainly comprised pericytes, epithelial cells, neurons, and other cell types. These findings collectively indicate that HOs possess a more comprehensive genetic repertoire of heart constituent cells in comparison to COs.
Increased sensitivity to ischemic injury and ischemic-reperfusion (IR) injury in HOs
With the established HOs, we mimicked the pathological conditions of acute myocardial infarction (AMI) and subsequent cardiac fibrosis to model human heart disease (Fig. 4A). To replicate hypoxia-induced ischemic conditions, we introduced 50 μM of cobalt chloride (CoCl2) [19] to the organoids along with glucose-depleted culture medium. This approach effectively elevated the expression of hypoxia-inducible factor-1α (HIF-1α) in both COs and HOs (Figs. 4B and S3).
In the clinical condition, the rapid reintroduction of blood flow post-reperfusion can lead to an immediate supply of oxygen and nutrients, triggering heightened inflammation and oxidative stress, thereby potentially causing tissue damage. A study suggested that high glucose sensitizes cardiomyocytes to ischemia-reperfusion (IR) injury [20]. Another study proposed that intracellular and mitochondrial calcium overload may contribute to reperfusion injury by exacerbating oxidative stress [21]. Based on these findings, we hypothesized that these factors could mimic reperfusion injury in CoCl2-treated HOs. To test this hypothesis, we applied a culture condition in which high glucose and calcium ion levels, then CoCl2-treated COs and HOs were exposed to a reperfusion medium rich in glucose and calcium ions for 72 h.
To verify the induction of apoptosis in both COs and HOs following IR injury, we performed co-staining of cTnT and cleaved caspase-3 in organoid sections (Fig. 4C). This co-staining provided confirmation of the reduction in cardiomyocytes and the increase in apoptosis were more pronounced in HOs compared to COs (Fig. 4C). Western blot analysis against the cleaved caspase-3 further confirmed the more effective induction of apoptosis in HOs relative to COs (Figs. 4D and S4). Validation of apoptosis in the IR-injured organoids was also carried out using the TUNEL assay, and the findings demonstrated the more increased apoptotic cells within the HOs than that of COs (Fig. 4E). Additionally, Western blot analysis unveiled a more substantial increase in the Bax/Bcl2 signaling in HOs compared to COs (Fig. S5).
IR-injured HOs exhibited characteristics of human AMI
IR injury in humans leads to the disruption of sarcomere structures and a reduction in cardiac markers, including cTnT and cTnI, within heart tissue [22]. Furthermore, in clinical practices, markers such as cTnI, Myoglobin (MB), and Creatine kinase M (CKM) are quantified in blood to diagnose myocardial infarction resulting from IR injury [23].
Consistent with previous findings, we observed a more pronounced disintegration of sarcomere structures in HOs following IR injury, in contrast to COs (Fig. 5A). Simultaneously, the intracellular expression of cTnT and cTnI showed a marked reduction in HOs compared to COs (Figs. 5B and S6). Moreover, the release of cTnI, MB, and CKM from HOs began to be released from the organoids 24 h post-IR injury, with the highest levels observed at 72 h and exhibited significantly higher levels than those from COs (Fig. 5C).
In addition, an analysis of inflammatory responses and necrosis-related mRNA levels in both COs and HOs following IR injury revealed a more notable increase in gene expressions within HOs in comparison to COs (Fig. S7A). Furthermore, HOs subjected to IR injury displayed a more significant upregulation of NF-κB, a crucial transcription factor involved in inflammation and processes related to cardiac-vascular damage, in comparison to IR-injured COs (Figs. S7B and S8). The expression levels of phosphorylated ERK, phosphorylated JNK, and phosphorylated p38, which are indicative of increased signaling pathways in cardiac remodeling post-AMI [24, 25], were also significantly elevated in IR-injured HOs compared to COs (Figs. S7C and S8).
Calcium overload and functional defects in IR-injured HOs
Intracellular calcium overload and subsequent mitochondrial calcium accumulation are observed in acute myocardial ischemia, and these phenomena are exacerbated during reperfusion, ultimately leading to mitochondrial permeability transition pore (mPTP) opening [26]. Furthermore, within a physiological environment, the bulk of calcium during cycles of contraction and relaxation is released from and taken up by the sarcoplasmic reticulum (SR) [27]. Therefore, quantifying SR calcium content is essential in elucidating the pathophysiological mechanisms of calcium overload.
We first observed calcium overload in the organoids by measuring the activity of sarco/endoplasmic reticulum calcium ATPase (SERCA), which significantly influences SR calcium storage [28], to infer the SR calcium content. Before IR injury, there were no significant differences in basal and peak intracellular calcium concentrations between COs and HOs during the contraction–relaxation cycle (Fig. 6A and B). However, after IR injury, both the basal and peak calcium concentrations were significantly higher in HOs compared to COs (Fig. 6A and B). Subsequently, we measured the activity of SERCA (kSERCA) by calculating the time constant after inhibiting SERCA and observed that the SERCA activity was notably increased in IR-injured HOs compared to IR-injured COs (Fig. 6C). In the same context, the phosphorylated phospholamban (PLN) expression was significantly elevated in IR-injured HOs, confirming the accelerated SERCA activity (Fig. 6D and S9). This suggests that SERCA activity preferentially increases during IR induction in HOs, leading to a significant increase in SR calcium storage in IR-injured HOs compared to IR-injured COs.
To determine whether the IR condition facilitates mPTP opening in HOs, we directly measured fluorescence intensity using an mPTP assay kit in the IR-injured organoids and found a more significant reduction in fluorescence intensity within IR-injured HOs compared to COs (Fig. 6E and F), suggesting that IR injury in HOs leads to a greater increase in mPTP opening than IR injury in COs.
Moreover, the real-time calcium transient assay allowed for an analysis of calcium handling properties in IR-injured organoids (Figs. 6G and S10). Amplitudes showed no significant difference between COs and HOs during ischemia and IR injury (Fig. 6G). However, HOs subjected to ischemia-injury exhibited aberrant beating properties (Fig. 6G) with a significant change in beating rate (peak-to-peak) and systolic time (time-to-peak), indicated a disease-like model. Consistent with the ischemia results, the IR-injury condition induced further detrimental calcium handling properties in HOs, resulting in a decrease in beating and systolic parameters compared to those of COs (Fig. 6G). Collectively, these results indicate that multicellular HOs effectively mimic clinically observed AMI pathologies, such as calcium overload and mPTP opening under IR conditions, as well as the mimicking defects in calcium handling function (Fig. 6H).
Modeling cardiac fibrosis in IR-injured HOs
Cardiac fibrosis is a consequential outcome of cardiac remodeling following AMI [29]. To replicate the cardiac fibrosis within IR-injured HOs, we cultured the organoids with 10 μM TGF-β1 for 7 days. Staining for COL1A1, a marker indicating fibrosis progression, revealed a more pronounced accumulation of collagen in IR-injured HOs after fibrosis induction compared to IR-injured COs (Fig. 7A and S12A). This substantial collagen accumulation in IR-injured HOs was further confirmed through western blot analysis and Masson’s trichrome (MT) staining (Fig. 7B, C and S12B). Additionally, we assessed increased expression levels of mRNA associated with fibrosis-related genes (ACTA2, POSTN, Vimentin, MMP2) and collagen-related genes (PAI1, COL1A1, COL1A2, COL3A1) in IR-injured HOs after fibrosis induction using quantitative PCR (Fig. S12C).
To validate the alterations in calcium handling in HOs under the IR-fibrosis condition, we conducted a calcium transient assay. Real-time video recordings allowed for an analysis of beating properties (Fig. S13A and Videos 11, 12) of the organoids, and HOs subjected to IR-fibrosis displayed an increase in amplitude and beating (peak-to-peak) but a decrease in systolic (time-to-peak) compared to IR-fibrosis COs (Fig. S13B), reflecting a form of arrhythmic event in the human heart.
Heart disease also leads to alterations in electrophysiological properties [30, 31]. To demonstrate the defect of electrophysiological characteristics in IR-fibrosis HOs, multielectrode arrays (MEA) were utilized (Fig. 7D). Consistent with the analysis of beating properties in calcium transient, the beating rate (BPM) was significantly increased in IR-fibrosis HOs compared to IR-fibrosis COs, and the BPM exceeded 100, a characteristic of tachycardia (Fig. 7E). The spike amplitude, indicative of action potential height, demonstrated a decline in both COs and HOs within the IR-fibrosis group, but HOs displayed a particularly significant difference compared to COs (Fig. 7E). Measurement of the field potential duration corrected by Fridericia’s formula (FPDcF) unveiled a twofold increase in HOs subjected to IR-fibrosis (Fig. 7E), mirroring the prolongation of the period between the onset of the Q wave and the conclusion of the T wave. The cardiac conduction velocity exhibited a significant slowing in IR-fibrosis HOs compared to IR-fibrosis COs, resulting from an elevated risk of re-entrant excitation attributing to collagen accumulation in HOs (Fig. 7E). Additionally, induction of fibrosis subsequent to IR injury resulted in reduced contractility of COs but maintained normal cardiac rhythms, whereas, in HOs, it led to both diminished contractility and irregular cardiac rhythms (Fig. 7F).
Further confirmation of heart disease modeling in HOs
The QuantSeq 3’ mRNA-Sequencing analysis provided further support for the modeling of AMI and cardiac fibrosis in HOs (Fig. 8). In comparing the up-regulated KEGG pathways between control HOs and IR-injured HOs (Fig. 8A), it was observed that the FoxO signaling pathway, known to be activated in cardiomyocytes under ischemic stress [32], was predominantly up-regulated. Additionally, pathways associated with cancer, which share common systemic pathology and mechanisms with heart failure [33], were also up-regulated in IR-injured HOs. Furthermore, pathways related to extracellular matrix (ECM)-receptor interaction, PI3K-Akt signaling, and HIF-1 signaling were up-regulated in IR-injured HOs compared to control HOs which are known to play crucial roles in cardiac remodeling [34], alleviating negative post-infarct changes in myocardium [35], and modulating post-infarct healing after myocardial ischemic injury [36], respectively. Interestingly, pathways associated with human papillomavirus, insulin resistance, efferocytosis, longevity genes, and focal adhesion kinase (FAK) inhibition were also found to be up-regulated in IR-injured HOs. These pathways are implicated in various processes such as the diagnosis of myocardial infarction [37], hypoxia-induced inhibition of angiogenesis [38], macrophage-mediated clearance of dead cells during myocardial infarction [39], modulation of cardiovascular function [40], and regulation of cardiac fibrosis post-MI [41].
The comparison between control HOs and IR-fibrosis HOs revealed up-regulated pathways associated with cardiac fibrosis (Fig. 8B). One of the pathways identified as up-regulated in IR-fibrosis HOs, is the calcium signaling pathway, known to play a role in fibroblast activation by increasing intracellular calcium concentration, promoting fibroblast proliferation and migration, and inducing the synthesis of extracellular matrix proteins [42]. Extracellular matrix (ECM) remodeling is closely linked to cardiac remodeling and the development of heart failure [43]. Furthermore, the renin-angiotensin-aldosterone system (RAAS) pathway, Wnt signaling pathway, and adrenergic signaling pathway were also identified as up-regulated in IR-fibrosis HOs. These pathways are known to promote myocardial fibrosis and cardiac remodeling, contributing to the progression of heart failure [44,45,46,47], respectively. Additionally, conditions such as Cushing syndrome, circadian disruption, and cardiomyopathy, which are associated with increased myocardial fibrosis [48,49,50], were found to be relevant to the up-regulated pathways in IR-fibrosis HOs. Cortisol is also experimentally shown to induce cardiomyocyte hypertrophy [51].
Discussion
This study demonstrates the successful generation of multi-cellular heart organoids (HOs) from hiPSCs through in vitro self-organization. In native development, structural maturation is orchestrated by cell-cell interactions and associated physical transformations [52]. Crucially, these interactions initiate during early development [53]. Reports indicate that factors secreted by other cells, such as endothelial cells, fibroblasts, and inflammatory cells, facilitate the maturation of functional and structural cardiomyocytes [54]. Consequently, we devised HOs, leveraging differentiation signals within 3D embryoid bodies to prompt multicellular configuration, thereby achieving optimal adult-like maturation timelines.
Traditionally, disease modeling using cell models has primarily centered around genetic disorders, while attempts to recreate adult-onset conditions in vitro have been limited. Notably, a recent experiment involving oxygen gradients generated organoids with infarct-like characteristics, showing various disease features [17]. However, these methods do not authentically replicate the intricate pathology of myocardial infarction (MI) because they tend to focus on replicating specific events, such as ischemia. Conversely, our study took a systematic approach by inducing ischemia and ischemia-reperfusion (IR) injury in HOs through precisely defined chemical culture conditions.
Hypoxia chambers have traditionally been utilized for inducing hypoxia in in vitro cell cultures. However, a challenge arises from the fact that hypoxia-inducible factors, which act as sensors of hypoxia and regulators of cellular hypoxic responses, are continuously synthesized under hypoxic conditions but rapidly degraded upon returning the cell culture to normoxia conditions. To address this challenge, we employed a widely used hypoxia-inducing agent, cobalt chloride (CoCl2), to induce hypoxia in HOs. CoCl2 effectively stabilized the expression of hypoxia-inducible factors 1α and 2α during prolonged culture of HOs. This approach ensures a continuous induction of hypoxia, providing a more sustained environment compared to traditional hypoxia chambers. Additionally, by subsequent rapid nutrient supply and calcium overload in the CoCl2-treated HOs, we effectively induced a response in HOs that closely resembled the physiological changes observed in human MI. These IR-induced HOs exhibited characteristic features of acute AMI, including specific cell death in the myocyte population, release of relevant biomarkers, increased inflammatory responses, and functional impairments.
We suggest that HOs may exhibit a more pronounced apoptotic response to hypoxic conditions compared to COs. Ischemia-reperfusion (IR) injury, which is a primary driver of cardiac disease, is known to primarily induce apoptosis-induced cell death, particularly affecting endothelial cells more than cardiomyocytes [55]. Endothelial cells also play a crucial role in modulating the inflammatory responses associated with IR injury and myocardial infarction [56] Thus, we presume that the increased population of endothelial cells in HOs may contribute to the more sensitive responses to hypoxia-induced apoptosis and the heightened production of inflammatory factors observed after IR injury. This highlights the advantage of utilizing HOs for modeling cardiac diseases and studying their pathophysiological mechanisms, particularly in the context of ischemic conditions.
Certainly, the success in mimicking acute MI and cardiac fibrosis using HOs in this study is a significant step forward. However, considerations should be given to incorporating additional cell types, such as mural cells (pericytes and vascular smooth muscle cells) and immune cells (myeloid and lymphoid cells), as their interactions play a role in human cardiovascular diseases [56, 57]. Nonetheless, the HOs in this study demonstrated the successful generation of self-organized major cellular compositions found in the ventricles of human hearts. Notably, heart diseases such as acute AMI and cardiac fibrosis were effectively recapitulated under defined culture conditions, showing defects in phenotypes and functional impairments. While many studies have reported heart disease induction at the cellular level, this study stands out by uniquely demonstrating the impairment of calcium ion handling, electrical activity, and contractility. These specific observations provide a comprehensive reflection of cardiac functions. As a result, this study introduces a promising heart organoid model derived from hiPSCs.
Data availability
The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.
References
Zhao Z, Chen X, Dowbaj AM, Sljukic A, Bratlie K, Lin L, et al. Organoids. Nat Rev Methods Primers. 2022;2:94.
Fan C, He J, Xu S, Yan J, Jin L, Dai J, Hu B. Advances in biomaterial-based cardiac organoids. Biomater Adv. 2023;153:213502.
Correia CD, Ferreira A, Fernandes MT, Silva BM, Esteves F, Leitao HS, et al. Human stem cells for cardiac disease modeling and preclinical and clinical applications—are we on the road to success? Cells. 2023;12:1727.
Vunjak-Novakovic G. Cardiac biology: a protein for healing infarcted hearts. Nature. 2015;525:461–2.
Arslan U, Brescia M, Meraviglia V, Nahon DM, van Helden RWJ, Stein JM, et al. Vascularized hiPSC-derived 3D cardiac microtissue on chip. Stem Cell Rep. 2023;18:1394–404.
Polonchuk L, Surija L, Lee MH, Sharma P, Liu Chung Ming C, Richter F, et al. Towards engineering heart tissues from bioprinted cardiac spheroids. Biofabrication. 2021;13:045009.
Scalise M, Marino F, Salerno L, Cianflone E, Molinaro C, Salerno N, et al. From spheroids to organoids: the next generation of model systems of human cardiac regeneration in a dish. Int J Mol Sci. 2021;22:13180.
Drakhlis L, Biswanath S, Farr CM, Lupanow V, Teske J, Ritzenhoff K, et al. Human heart-forming organoids recapitulate early heart and foregut development. Nat Biotechnol. 2021;39:737–46.
Lee SG, Kim YJ, Son MY, Oh MS, Kim J, Ryu B, et al. Generation of human iPSCs derived heart organoids structurally and functionally similar to heart. Biomaterials. 2022;290:121860.
Ghosheh M, Ehrlich A, Ioannidis K, Ayyash M, Goldfracht I, Cohen M, et al. Electro-metabolic coupling in multi-chambered vascularized human cardiac organoids. Nat Biomed Eng. 2023;7:1493–513.
Hofbauer P, Jahnel SM, Papai N, Giesshammer M, Deyett A, Schmidt C, et al. Cardioids reveal self-organizing principles of human cardiogenesis. Cell. 2021;184:3299–317.e22.
Zhao D, Lei W, Hu S. Cardiac organoid—a promising perspective of preclinical model. Stem Cell Res Ther. 2021;12:272.
Kim SK, Kim YH, Park S, Cho SW. Organoid engineering with microfluidics and biomaterials for liver, lung disease, and cancer modeling. Acta Biomater. 2021;132:37–51.
Skardal A, Shupe T, Atala A. Organoid-on-a-chip and body-on-a-chip systems for drug screening and disease modeling. Drug Discov Today. 2016;21:1399–411.
Kratochvil MJ, Seymour AJ, Li TL, Pasca SP, Kuo CJ, Heilshorn SC. Engineered materials for organoid systems. Nat Rev Mater. 2019;4:606–22.
Voges HK, Mills RJ, Elliott DA, Parton RG, Porrello ER, Hudson JE. Development of a human cardiac organoid injury model reveals innate regenerative potential. Development. 2017;144:1118–27.
Richards DJ, Li Y, Kerr CM, Yao J, Beeson GC, Coyle RC, et al. Human cardiac organoids for the modelling of myocardial infarction and drug cardiotoxicity. Nat Biomed Eng. 2020;4:446–62.
Lee H, Im JS, Choi DB, An J, Kim S-B, Yeon S, et al. Three-dimensional cardiac organoid formation accelerates the functional maturation of human induced pluripotent stem cell-derived cardiomyocytes. Organoid. 2022;2:e14.
Rana NK, Singh P, Koch B. CoCl(2) simulated hypoxia induce cell proliferation and alter the expression pattern of hypoxia associated genes involved in angiogenesis and apoptosis. Biol Res. 2019;52:12.
Luan R, Liu S, Yin T, Lau WB, Wang Q, Guo W, et al. High glucose sensitizes adult cardiomyocytes to ischaemia/reperfusion injury through nitrative thioredoxin inactivation. Cardiovasc Res. 2009;83:294–302.
Piper HM, Abdallah Y, Schafer C. The first minutes of reperfusion: a window of opportunity for cardioprotection. Cardiovasc Res. 2004;61:365–71.
de Winter RJ, Koster RW, Sturk A, Sanders GT. Value of myoglobin, troponin T, and CK-MBmass in ruling out an acute myocardial infarction in the emergency room. Circulation. 1995;92:3401–7.
de Winter RJ, Koster RW, Schotveld JH, Sturk A, van Straalen JP, Sanders GT. Prognostic value of troponin T, myoglobin, and CK-MB mass in patients presenting with chest pain without acute myocardial infarction. Heart. 1996;75:235–9.
Kacimi R, Gerdes AM. Alterations in G protein and MAP kinase signaling pathways during cardiac remodeling in hypertension and heart failure. Hypertension. 2003;41:968–77.
Kehat I, Molkentin JD. Molecular pathways underlying cardiac remodeling during pathophysiological stimulation. Circulation. 2010;122:2727–35.
Ruiz-Meana M, Garcia-Dorado D, Miro-Casas E, Abellan A, Soler-Soler J. Mitochondrial Ca2+ uptake during simulated ischemia does not affect permeability transition pore opening upon simulated reperfusion. Cardiovasc Res. 2006;71:715–24.
Eisner D, Neher E, Taschenberger H, Smith G. Physiology of intracellular calcium buffering. Physiol Rev. 2023;103:2767–845.
Diaz ME, Graham HK, Trafford AW. Enhanced sarcolemmal Ca2+ efflux reduces sarcoplasmic reticulum Ca2+ content and systolic Ca2+ in cardiac hypertrophy. Cardiovasc Res. 2004;62:538–47.
Yellon DM, Hausenloy DJ. Myocardial reperfusion injury. N Engl J Med. 2007;357:1121–35.
Janse MJ. Electrophysiological changes in heart failure and their relationship to arrhythmogenesis. Cardiovasc Res. 2004;61:208–17.
Akar FG, Rosenbaum DS. Transmural electrophysiological heterogeneities underlying arrhythmogenesis in heart failure. Circ Res. 2003;93:638–45.
Xin Z, Ma Z, Jiang S, Wang D, Fan C, Di S, et al. FOXOs in the impaired heart: new therapeutic targets for cardiac diseases. Biochim Biophys Acta Mol Basis Dis. 2017;1863:486–98.
de Boer RA, Hulot JS, Tocchetti CG, Aboumsallem JP, Ameri P, Anker SD, et al. Common mechanistic pathways in cancer and heart failure. A scientific roadmap on behalf of the Translational Research Committee of the Heart Failure Association (HFA) of the European Society of Cardiology (ESC). Eur J Heart Fail. 2020;22:2272–89.
Hochman JS, Bulkley BH. Expansion of acute myocardial infarction: an experimental study. Circulation. 1982;65:1446–50.
Walkowski B, Kleibert M, Majka M, Wojciechowska M. Insight into the role of the PI3K/Akt pathway in ischemic injury and post-infarct left ventricular remodeling in normal and diabetic heart. Cells. 2022;11:1553.
Wang T, Xiao Y, Zhang J, Jing F, Zeng G. Dynamic regulation of HIF-1 signaling in the rhesus monkey heart after ischemic injury. BMC Cardiovasc Disord. 2022;22:407.
Joo EJ, Chang Y, Kwon MJ, Cho A, Cheong HS, Ryu S. High-risk human papillomavirus infection and the risk of cardiovascular disease in Korean women. Circ Res. 2019;124:747–56.
Aroor AR, Mandavia CH, Sowers JR. Insulin resistance and heart failure: molecular mechanisms. Heart Fail Clin. 2012;8:609–17.
Prabhu SD, Frangogiannis NG. The biological basis for cardiac repair after myocardial infarction: from inflammation to fibrosis. Circ Res. 2016;119:91–112.
Liberale L, Kraler S, Camici GG, Luscher TF. Ageing and longevity genes in cardiovascular diseases. Basic Clin Pharmacol Toxicol. 2020;127:120–31.
Fan GP, Wang W, Zhao H, Cai L, Zhang PD, Yang ZH, et al. Pharmacological inhibition of focal adhesion kinase attenuates cardiac fibrosis in mice cardiac fibroblast and post-myocardial-infarction models. Cell Physiol Biochem. 2015;37:515–26.
Zhang X, Zhang T, Wu J, Yu X, Zheng D, Yang F, et al. Calcium sensing receptor promotes cardiac fibroblast proliferation and extracellular matrix secretion. Cell Physiol Biochem. 2014;33:557–68.
Cohn JN, Ferrari R, Sharpe N. Cardiac remodeling–concepts and clinical implications: a consensus paper from an international forum on cardiac remodeling. Behalf of an International Forum on Cardiac Remodeling. J Am Coll Cardiol. 2000;35:569–82.
Brilla CG. Renin-angiotensin-aldosterone system and myocardial fibrosis. Cardiovasc Res. 2000;47:1–3.
Stylianidis V, Hermans KCM, Blankesteijn WM. Wnt signaling in cardiac remodeling and heart failure. Handb Exp Pharmacol. 2017;243:371–93.
Dang S, Zhang ZY, Li KL, Zheng J, Qian LL, Liu XY, et al. Blockade of beta-adrenergic signaling suppresses inflammasome and alleviates cardiac fibrosis. Ann Transl Med. 2020;8:127.
Tanner MA, Thomas TP, Maitz CA, Grisanti LA. beta2-adrenergic receptors increase cardiac fibroblast proliferation through the Galphas/ERK1/2-dependent secretion of interleukin-6. Int J Mol Sci. 2020;21:8507.
Yiu KH, Marsan NA, Delgado V, Biermasz NR, Holman ER, Smit JW, et al. Increased myocardial fibrosis and left ventricular dysfunction in Cushing’s syndrome. Eur J Endocrinol. 2012;166:27–34.
Rabinovich-Nikitin I, Lieberman B, Martino TA, Kirshenbaum LA. Circadian-regulated cell death in cardiovascular diseases. Circulation. 2019;139:965–80.
Tian J, An X, Niu L. Myocardial fibrosis in congenital and pediatric heart disease. Exp Ther Med. 2017;13:1660–4.
Kanzaki A, Kadoya M, Katayama S, Koyama H. Cardiac hypertrophy and related dysfunctions in cushing syndrome patients-literature review. J Clin Med. 2022;11:7035.
Kupfer ME, Lin WH, Ravikumar V, Qiu K, Wang L, Gao L, et al. In situ expansion, differentiation, and electromechanical coupling of human cardiac muscle in a 3D bioprinted, chambered organoid. Circ Res. 2020;127:207–24.
Hoang P, Wang J, Conklin BR, Healy KE, Ma Z. Generation of spatial-patterned early-developing cardiac organoids using human pluripotent stem cells. Nat Protoc. 2018;13:723–37.
Mills RJ, Hudson JE. There’s No I in Team: cellular crosstalk enhances in vitro cardiac maturation. Cell Stem Cell. 2020;26:799–801.
Maseri A, Beltrame JF, Shimokawa H. Role of coronary vasoconstriction in ischemic heart disease and search for novel therapeutic targets. Circ J. 2009;73:394–403.
Zhuge Y, Zhang J, Qian F, Wen Z, Niu C, Xu K, et al. Role of smooth muscle cells in cardiovascular disease. Int J Biol Sci. 2020;16:2741–51.
Ramel D, Gayral S, Sarthou MK, Auge N, Negre-Salvayre A, Laffargue M. Immune and smooth muscle cells interactions in atherosclerosis: how to target a breaking bad dialogue? Front Pharmacol. 2019;10:1276.
Acknowledgements
This study was supported by grants from the National Research Foundation, which is funded by the Ministry of Science and ICT of Korea (No. 2019M3A9H1103718) and the Ministry of Food and Drug Safety (22213MFDS393).
Author information
Authors and Affiliations
Contributions
Myeongjin Song: Conceptualization, experimentation, data analysis and visualization, and original draft writing. Da Bin Choi, Jeong Suk Im, Ye Na Song, Ji Hyun Kim, Hanbyeol Lee, and Young Keul Jeon: Experimentation, sample preparation, and data analysis. Jieun An, Ami Kim, Hwan Choi, Joon-Chul Kim, Choongseong Han, and Sung Joon Kim: Contribution to result interpretation. Dong-Hun Woo: Conceptualization, supervision, manuscript writing, review, editing, and funding acquisition.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing interests.
Ethical approval and consent to participate
The fibroblasts used for generating iPSCs in this study were purchased from commercially available vendor ATCC and were therefore exempt from institutional review board approval.
Additional information
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Edited by Sergio Lavandero
Supplementary information
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Song, M., Choi, D.B., Im, J.S. et al. Modeling acute myocardial infarction and cardiac fibrosis using human induced pluripotent stem cell-derived multi-cellular heart organoids. Cell Death Dis 15, 308 (2024). https://doi.org/10.1038/s41419-024-06703-9
Received:
Revised:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41419-024-06703-9
- Springer Nature Limited