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一种交联环硅氧烷聚合物基质作为实现具有类原始特征的人类诱导多能干细胞长期培养的平台。

A Cross-Linked Cyclosiloxane Polymer Matrix as a Platform Enabling Long-Term Culture of Human Induced Pluripotent Stem Cells with Naïve-Like Features.

作者信息

Seo Changjin, Song Junhyuk, Choi Yoonjung, Kim Taemook, Lee Daeyoup, Jon Sangyong

机构信息

Department of Biological Sciences, KAIST Institute for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.

Center for Precision Bio-Nanomedicine, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.

出版信息

Biomater Res. 2025 Apr 28;29:0197. doi: 10.34133/bmr.0197. eCollection 2025.

DOI:10.34133/bmr.0197
PMID:40296880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12034926/
Abstract

Culture platforms for human induced pluripotent stem cells (hiPSCs) that rely on feeder cells or extracellular matrices (ECMs) face substantial limitations for practical regenerative medicine applications, including undefined components, high costs, and a tendency to maintain hiPSCs in the primed pluripotent state, which has lower differentiation potential than the naïve state. To overcome these challenges, we developed a long-term hiPSC culture platform based on a cross-linked cyclosiloxane polymer matrix that preserves pluripotency with naïve-like characteristics. Through optimization, we identified an ideal cyclosiloxane polymer matrix, designated as poly-Z, which supported the growth of hiPSCs as spheroids. Even after 60 d of continuous culture, hiPSC spheroids maintained on poly-Z retained pluripotency markers and normal karyotypes at levels comparable to those of hiPSC colonies cultured on conventional vitronectin (VN)-coated plates. Furthermore, mRNA sequencing revealed that hiPSC spheroids cultured on poly-Z not only exhibited up-regulation of typical pluripotency-related genes but also showed increased expression of genes associated with the naïve pluripotent state, in contrast to the primed state observed in hiPSCs cultured on VN-coated plates or in suspension culture. Gene ontology (GO) analysis and gene set enrichment analysis (GSEA) further suggested that the down-regulation of genes involved in cell-ECM interactions contributed to the induction of naïve-like features in poly-Z-cultured hiPSC spheroids. These findings highlight the potential of cross-linked cyclosiloxane-based polymer matrices as an innovative platform for human pluripotent stem cell research and regenerative medicine.

摘要

依赖饲养层细胞或细胞外基质(ECM)的人诱导多能干细胞(hiPSC)培养平台在实际再生医学应用中面临重大限制,包括成分不明确、成本高以及倾向于将hiPSC维持在始发态多能状态,而始发态多能状态的分化潜能低于原始态。为了克服这些挑战,我们开发了一种基于交联环硅氧烷聚合物基质的长期hiPSC培养平台,该平台可保留具有原始态样特征的多能性。通过优化,我们确定了一种理想的环硅氧烷聚合物基质,命名为聚-Z,它支持hiPSC作为球体生长。即使连续培养60天,维持在聚-Z上的hiPSC球体仍保留多能性标记和正常核型,其水平与在传统玻璃粘连蛋白(VN)包被板上培养的hiPSC集落相当。此外,mRNA测序显示,与在VN包被板上或悬浮培养中观察到的始发态hiPSC相比,在聚-Z上培养的hiPSC球体不仅表现出典型多能性相关基因的上调,还显示出与原始多能状态相关基因的表达增加。基因本体(GO)分析和基因集富集分析(GSEA)进一步表明,参与细胞-ECM相互作用的基因下调有助于在聚-Z培养的hiPSC球体中诱导原始态样特征。这些发现突出了基于交联环硅氧烷的聚合物基质作为人类多能干细胞研究和再生医学创新平台的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/0b0edbc72a56/bmr.0197.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/1681133f9318/bmr.0197.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/73a1aa5617c1/bmr.0197.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/5405677163a3/bmr.0197.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/b81b20bb7cc6/bmr.0197.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/68ff663c058a/bmr.0197.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/fefb406e2b92/bmr.0197.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/0b0edbc72a56/bmr.0197.fig.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/1681133f9318/bmr.0197.fig.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/73a1aa5617c1/bmr.0197.fig.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/5405677163a3/bmr.0197.fig.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/b81b20bb7cc6/bmr.0197.fig.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/68ff663c058a/bmr.0197.fig.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/fefb406e2b92/bmr.0197.fig.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8662/12034926/0b0edbc72a56/bmr.0197.fig.007.jpg

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