Engineering a robust and anisotropic cardiac-specific extracellular matrix scaffold for cardiac patch tissue engineering

Q1 Medicine Matrix Biology Plus Pub Date : 2024-05-25 DOI:10.1016/j.mbplus.2024.100151
Te-An Chen , Brandon B. Zhao , Richard A. Balbin , Sameeksha Sharma , Donggi Ha , Timothy J. Kamp , Yuxiao Zhou , Feng Zhao
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Abstract

Extracellular matrix (ECM) fabricated using human induced pluripotent stem cells (hiPSCs)-derived cardiac fibroblasts (hiPSC-CFs) could serve as a completely biological scaffold for an engineered cardiac patch, leveraging the unlimited source and outstanding reproducibility of hiPSC-CFs. Additionally, hiPSC-CF-derived ECM (hiPSC-CF-ECM) holds the potential to enhance maturation of exogenous cardiomyocytes, such as hiPSC-derived cardiomyocytes (hiPSC-CMs), by providing a microenvironment rich in cardiac-specific biochemical and signaling cues. However, achieving sufficient robustness of hiPSC-CF-ECM is challenging. This study aims to achieve appropriate ECM deposition, scaffold thickness, and mechanical strength of an aligned hiPSC-CF-ECM by optimizing the culture period, ranging from 2 to 10 weeks, of hiPSC-CFs grown on micro-grated substrates, which can direct the alignment of both hiPSC-CFs and their secreted ECM. The hiPSC-CFs demonstrated a production rate of 13.5 µg ECM per day per 20,000 cells seeded. An anisotropic nanofibrous hiPSC-CF-ECM scaffold with a thickness of 20.0 ± 2.1 µm was achieved after 6 weeks of culture, followed by decellularization. Compositional analysis through liquid chromatography-mass spectrometry (LC-MS) revealed the presence of cardiac-specific fibrillar collagens, non-fibrillar collagens, and matricellular proteins. Uniaxial tensile stretching of the hiPSC-CF-ECM scaffold indicated robust tensile resilience. Finally, hiPSCs-CMs cultured on the hiPSC-CF-ECM exhibited alignment following the guidance of ECM nanofibers and demonstrated mature organization of key structural proteins. The culture duration of the anisotropic hiPSC-CF-ECM was successfully refined to achieve a robust scaffold containing structural proteins that resembles cardiac microenvironment. This completely biological, anisotropic, and cardiac-specific ECM holds great potential for cardiac patch engineering.

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为心脏补片组织工程设计一种坚固且各向异性的心脏特异性细胞外基质支架
利用人体诱导多能干细胞(hiPSCs)衍生的心脏成纤维细胞(hiPSC-CFs)制造的细胞外基质(ECM)可作为工程心脏补片的完全生物支架,充分利用了hiPSC-CFs的无限来源和出色的可重复性。此外,hiPSC-CF 衍生的 ECM(hiPSC-CF-ECM)通过提供富含心脏特异性生化和信号线索的微环境,有可能促进外源性心肌细胞(如 hiPSC 衍生的心肌细胞(hiPSC-CMs))的成熟。然而,要使 hiPSC-CF-ECM 具有足够的稳健性是一项挑战。本研究旨在通过优化生长在微栅格基底上的 hiPSC-CF 的培养期(2 到 10 周不等),实现对齐的 hiPSC-CF-ECM 的适当 ECM 沉积、支架厚度和机械强度。hiPSC-CFs 的生产率为每 20000 个细胞每天生产 13.5 µg ECM。培养 6 周后,各向异性的纳米纤维状 hiPSC-CF-ECM 支架形成,厚度为 20.0 ± 2.1 µm,随后进行脱细胞处理。通过液相色谱-质谱法(LC-MS)进行的成分分析显示,存在心脏特异性纤维胶原、非纤维胶原和母细胞蛋白。对 hiPSC-CF-ECM 支架的单轴拉伸表明其具有强大的拉伸韧性。最后,在 hiPSC-CF-ECM 上培养的 hiPSCs-CMs 在 ECM 纳米纤维的引导下排列整齐,并显示出关键结构蛋白的成熟组织。各向异性 hiPSC-CF-ECM 的培养持续时间得到了成功的改进,从而获得了与心脏微环境相似的含有结构蛋白的稳健支架。这种完全生物的、各向异性的、心脏特异性 ECM 为心脏补片工程提供了巨大的潜力。
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来源期刊
Matrix Biology Plus
Matrix Biology Plus Medicine-Histology
CiteScore
9.00
自引率
0.00%
发文量
25
审稿时长
105 days
期刊最新文献
Revealing sex-specific changes across protein structure in the aging bone extracellular matrix P-LM421E8, the heparan sulfate chain-conjugated laminin-421-E8 fragment, drives differentiation of human induced pluripotent stem cells into hematopoietic progenitor cells comparable to basic fibroblast growth factor in a chemically defined system Generation of a conditional Adamts6 mouse allele reveals roles in lung maturation in addition to cardiac and musculoskeletal development Corrigendum to “Presence of type IIB procollagen in mouse articular cartilage and growth plate is revealed by immuno-histochemical analysis with a novel specific antibody” [Matrix Biol. Plus 18 (2023) 100130] Convergence research in matrix biology and biomaterials science
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