Long‐Term Culture of Human Pluripotent Stem Cells in Xeno‐Free Condition Using Functional Polymer Films

Author:

Cho Younghak12ORCID,Lee Hana3,Jeong Wonji2,Jung Kwang Bo3,Lee Sun Young4,Park Seonghyeon2,Yeun Jemin2,Kwon Ohman3,Son Jin Gyeong4,Lee Tae Geol4,Son Mi‐Young356,Im Sung Gap2ORCID

Affiliation:

1. Brain Science Institute Korea Institute of Science and Technology (KIST) 5, Hwarang‐ro 14‐gil, Seongbuk‐gu Seoul 02792 Republic of Korea

2. Functional Thin Film Laboratory Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

3. Korea Research Institute of Bioscience and Biotechnology (KRIBB) Daejeon 34141 Republic of Korea

4. Korea Research Institute of Standards and Science (KRISS) Daejeon 34141 Republic of Korea

5. KRIBB School of Bioscience Korea University of Science and Technology (UST) Daejeon 34113 Republic of Korea

6. Department of Biological Science Sungkyunkwan University Suwon 16419 Republic of Korea

Abstract

AbstractHuman pluripotent stem cells (hPSCs), encompassing human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs), hold immense potential in regenerative medicine, offering new opportunities for personalized cell therapies. However, their clinical translation is hindered by the inevitable reliance on xenogeneic components in culture environments. This study addresses this challenge by engineering a fully synthetic, xeno‐free culture substrate, whose surface composition is tailored systematically for xeno‐free culture of hPSCs. A functional polymer surface, pGC2 (poly(glycidyl methacrylate‐grafting‐guanidine‐co‐carboxylic acrylate)), offers excellent cell‐adhesive properties as well as non‐cytotoxicity, enabling robust hESCs and hiPSCs growth while presenting cost‐competitiveness and scalability over Matrigel. This investigation includes comprehensive evaluations of pGC2 across diverse experimental conditions, demonstrating its wide adaptability with various pluripotent stem cell lines, culture media, and substrates. Crucially, pGC2 supports long‐term hESCs and hiPSCs expansion, up to ten passages without compromising their stemness and pluripotency. Notably, this study is the first to confirm an identical proteomic profile after ten passages of xeno‐free cultivation of hiPSCs on a polymeric substrate compared to Matrigel. The innovative substrate bridges the gap between laboratory research and clinical translation, offering a new promising avenue for advancing stem cell‐based therapies.

Funder

National Research Foundation of Korea

Korea Research Institute of Bioscience and Biotechnology

Ministry of Health and Welfare

Ministry of Science and ICT, South Korea

Ministry of Trade, Industry and Energy

Publisher

Wiley

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