{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Li S"],"funding":["Shanghai \"Rising Stars of Medical Talents\" Youth Development Program","Program of Shanghai Academic/Technology Research Leader","Program of Shanghai Academic Research Leader","Shanghai Jiao Tong University School of Medicine","National Natural Science Foundation of China","Shanghai Key Clinical Specialty and Shanghai Eye Disease Research Center","School of Medicine, Shanghai Jiao Tong University"],"pagination":["e04732"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12376501"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["12(31)"],"pubmed_abstract":["The differentiation and stemness maintenance of stem cells are the core topics in cell biology and regenerative medicine, involving cell fate determination, developmental regulation and tissue regeneration. Chirality is an essential factor influencing multiple biological processes, including protein interactions, stem cell development and disease pathogenesis. However, its roles in regulating stem cells fate, especially limbal epithelial stem cells (LESCs), remain elusive. Herein, it is first discovered that right-handed chiral hydrogel (DH) enhanced LESCs proliferation, migration, and differentiation into corneal epithelial cells, while left-handed chiral hydrogel (LH) can partially preserve LESCs stemness. Further in vivo experiments demonstrated that 3D DH effectively accelerated corneal wound healing process, inhibited both inflammation and vascularization in a partial limbal stem cell deficiency model. Mechanistically, DH activates Notch signaling by increasing its stereo-affinity to Notch1, facilitating Notch intracellular domain release and HES1 transcription, thereby directing LESCs fate. Collectively, this work highlights the novel role of chirality in LESCs fate determination and confirms DH as a drug-free, effective approach for corneal epithelial regeneration, offering a new direction for regenerative medicine and tissue engineering."],"journal":["Advanced science (Weinheim, Baden-Wurttemberg, Germany)"],"pubmed_title":["Chirality Regulates Stem Cell Fate and Promotes Corneal Epithelial Regeneration via Manipulating Notch Pathway."],"pmcid":["PMC12376501"],"funding_grant_id":["82271041","22XD1401800","SHWSRS(2025)_71","2022ZZ01003","82201136","2022LHA06","82070919"],"pubmed_authors":["Li S","Chen J","Wu N","Chen L","Wu B","Fu Y","Sun H","Feng C","Zhao Y"],"additional_accession":[]},"is_claimable":false,"name":"Chirality Regulates Stem Cell Fate and Promotes Corneal Epithelial Regeneration via Manipulating Notch Pathway.","description":"The differentiation and stemness maintenance of stem cells are the core topics in cell biology and regenerative medicine, involving cell fate determination, developmental regulation and tissue regeneration. Chirality is an essential factor influencing multiple biological processes, including protein interactions, stem cell development and disease pathogenesis. However, its roles in regulating stem cells fate, especially limbal epithelial stem cells (LESCs), remain elusive. Herein, it is first discovered that right-handed chiral hydrogel (DH) enhanced LESCs proliferation, migration, and differentiation into corneal epithelial cells, while left-handed chiral hydrogel (LH) can partially preserve LESCs stemness. Further in vivo experiments demonstrated that 3D DH effectively accelerated corneal wound healing process, inhibited both inflammation and vascularization in a partial limbal stem cell deficiency model. Mechanistically, DH activates Notch signaling by increasing its stereo-affinity to Notch1, facilitating Notch intracellular domain release and HES1 transcription, thereby directing LESCs fate. Collectively, this work highlights the novel role of chirality in LESCs fate determination and confirms DH as a drug-free, effective approach for corneal epithelial regeneration, offering a new direction for regenerative medicine and tissue engineering.","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Aug","modification":"2026-05-09T19:15:13.305Z","creation":"2026-04-08T01:11:06.276Z"},"accession":"S-EPMC12376501","cross_references":{"pubmed":["40444446"],"doi":["10.1002/advs.202504732"]}}