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

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
{"title":"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","authors":"Te-An Chen ,&nbsp;Brandon B. Zhao ,&nbsp;Richard A. Balbin ,&nbsp;Sameeksha Sharma ,&nbsp;Donggi Ha ,&nbsp;Timothy J. Kamp ,&nbsp;Yuxiao Zhou ,&nbsp;Feng Zhao","doi":"10.1016/j.mbplus.2024.100151","DOIUrl":null,"url":null,"abstract":"<div><p>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.</p></div>","PeriodicalId":52317,"journal":{"name":"Matrix Biology Plus","volume":"23 ","pages":"Article 100151"},"PeriodicalIF":0.0000,"publicationDate":"2024-05-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590028524000115/pdfft?md5=bd5e6b9cc1d1b9530b6d246976193eea&pid=1-s2.0-S2590028524000115-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Engineering a robust and anisotropic cardiac-specific extracellular matrix scaffold for cardiac patch tissue engineering\",\"authors\":\"Te-An Chen ,&nbsp;Brandon B. Zhao ,&nbsp;Richard A. Balbin ,&nbsp;Sameeksha Sharma ,&nbsp;Donggi Ha ,&nbsp;Timothy J. Kamp ,&nbsp;Yuxiao Zhou ,&nbsp;Feng Zhao\",\"doi\":\"10.1016/j.mbplus.2024.100151\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>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.</p></div>\",\"PeriodicalId\":52317,\"journal\":{\"name\":\"Matrix Biology Plus\",\"volume\":\"23 \",\"pages\":\"Article 100151\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2590028524000115/pdfft?md5=bd5e6b9cc1d1b9530b6d246976193eea&pid=1-s2.0-S2590028524000115-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Matrix Biology Plus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590028524000115\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matrix Biology Plus","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590028524000115","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Engineering a robust and anisotropic cardiac-specific extracellular matrix scaffold for cardiac patch tissue engineering

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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
A human stem cell-derived model reveals pathologic extracellular matrix remodeling in diabetic podocyte injury Bone quality relies on hyaluronan synthesis – Insights from mice with complete knockout of hyaluronan synthase expression Profiling of collagen and extracellular matrix deposition from cell culture using in vitro ExtraCellular matrix mass spectrometry imaging (ivECM-MSI) Obesity-driven changes in breast tissue exhibit a pro-angiogenic extracellular matrix signature The importance of matrix in cardiomyogenesis: Defined substrates for maturation and chamber specificity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1