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Article: Differentiation of human induced pluripotent stem cells into retinal pigment epithelium cells during culture on peptide-grafted hydrogels

TitleDifferentiation of human induced pluripotent stem cells into retinal pigment epithelium cells during culture on peptide-grafted hydrogels
Authors
Keywordshuman pluripotent stem cell
hydrogel
peptide
retinal pigment epithelium
subretinal transplantation
Issue Date2025
Citation
Regenerative Biomaterials, 2025, v. 12, article no. rbaf035 How to Cite?
AbstractA variety of novel peptide-grafted hydrogels, of which peptides were derived from vitronectin (PQVTRGDVFTMP) or the laminin β4 chain (PMQKMRGDVFSP), were prepared in this study. The peptide-grafted hydrogels promoted the adhesion, proliferation and colony formation of hiPSCs and maintained their pluripotency up to passage 5 under xeno-free conditions. We successfully generated RPE cells from hiPSCs using one of the most suitable xeno-free peptide-grafted hydrogels, KVN2CK (KGCGGKGG-PQVTRGDVFTMP), which was derived from vitronectin, and confirmed the effect of these hiPSC-derived RPE cells in a rat retinal degeneration model (Royal College of Surgeons (RCS) rats) via subretinal transplantation, when we investigated functional improvements in vision in RCS rats after the transplantation of hiPSC-derived RPE cells. Our novel peptide-grafted hydrogels provided a safe and robust platform for generating single-layer hiPSC-derived RPE cells under xeno-free conditions, which indicates the potential of these hydrogels for stem cell therapy for retinal degenerative diseases in the future.
Persistent Identifierhttp://hdl.handle.net/10722/365649
ISSN
2023 Impact Factor: 5.6
2023 SCImago Journal Rankings: 0.986

 

DC FieldValueLanguage
dc.contributor.authorLiu, Jun-
dc.contributor.authorLiu, Qian-
dc.contributor.authorGuo, Minmei-
dc.contributor.authorJiang, Chengyu-
dc.contributor.authorChen, Jianyang-
dc.contributor.authorWang, Ting-
dc.contributor.authorSung, Tzu Cheng-
dc.contributor.authorChou, Shih Jie-
dc.contributor.authorChiou, Shih Hwa-
dc.contributor.authorFan, Guoping-
dc.contributor.authorHiguchi, Akon-
dc.date.accessioned2025-11-05T09:46:36Z-
dc.date.available2025-11-05T09:46:36Z-
dc.date.issued2025-
dc.identifier.citationRegenerative Biomaterials, 2025, v. 12, article no. rbaf035-
dc.identifier.issn2056-3418-
dc.identifier.urihttp://hdl.handle.net/10722/365649-
dc.description.abstractA variety of novel peptide-grafted hydrogels, of which peptides were derived from vitronectin (PQVTRGDVFTMP) or the laminin β4 chain (PMQKMRGDVFSP), were prepared in this study. The peptide-grafted hydrogels promoted the adhesion, proliferation and colony formation of hiPSCs and maintained their pluripotency up to passage 5 under xeno-free conditions. We successfully generated RPE cells from hiPSCs using one of the most suitable xeno-free peptide-grafted hydrogels, KVN2CK (KGCGGKGG-PQVTRGDVFTMP), which was derived from vitronectin, and confirmed the effect of these hiPSC-derived RPE cells in a rat retinal degeneration model (Royal College of Surgeons (RCS) rats) via subretinal transplantation, when we investigated functional improvements in vision in RCS rats after the transplantation of hiPSC-derived RPE cells. Our novel peptide-grafted hydrogels provided a safe and robust platform for generating single-layer hiPSC-derived RPE cells under xeno-free conditions, which indicates the potential of these hydrogels for stem cell therapy for retinal degenerative diseases in the future.-
dc.languageeng-
dc.relation.ispartofRegenerative Biomaterials-
dc.subjecthuman pluripotent stem cell-
dc.subjecthydrogel-
dc.subjectpeptide-
dc.subjectretinal pigment epithelium-
dc.subjectsubretinal transplantation-
dc.titleDifferentiation of human induced pluripotent stem cells into retinal pigment epithelium cells during culture on peptide-grafted hydrogels-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1093/rb/rbaf035-
dc.identifier.scopuseid_2-s2.0-105006563365-
dc.identifier.volume12-
dc.identifier.spagearticle no. rbaf035-
dc.identifier.epagearticle no. rbaf035-
dc.identifier.eissn2056-3426-

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