Proliferation and differentiation of Wharton's jelly-derived mesenchymal stem cells on prgf-treated hydrogel scaffold

被引:1
作者
Pourjabbar, Bahareh [1 ]
Shams, Forough [2 ]
Keshel, Saeed Heidari [1 ,3 ]
Biazar, Esmaeil [4 ]
机构
[1] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Tissue Engn & Appl Cell Sci, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Sch Adv Technol Med, Dept Med Biotechnol, Tehran, Iran
[3] Shahid Beheshti Univ Med Sci, Med Nanotechnol & Tissue Engn Res Ctr, Tehran, Iran
[4] Islamic Azad Univ, Dept Biomed Engn, Tonekabon Branch, Tissue Engn Grp, Tonekabon, Iran
关键词
Corneal tissue regeneration; hydrogel scaffold; plasma rich in growth factors (PRGF); Wharton's jelly derived mesenchymal stem cells (WJMSCs); limbal epithelial stem cells (LESCs); PLATELET-RICH PLASMA; GROWTH-FACTORS PRGF; CORNEAL EPITHELIAL-CELLS; IN-VITRO; SILK FIBROIN; MECHANICAL-PROPERTIES; NERVE REGENERATION; AMNIOTIC MEMBRANE; RECONSTRUCTION; SURFACE;
D O I
10.1080/17460751.2024.2427513
中图分类号
Q813 [细胞工程];
学科分类号
摘要
BackgroundTo address the limitations of Cultivated Limbal Epithelial Transplantation (CLET) and the use of amniotic membrane (AM) in treating Limbal Stem Cell Deficiency (LSCD), we aimed to develop a Collagen/Silk Fibroin (Co/SF) scaffold enriched with Platelet-Rich Growth Factor (PRGF) to support the proliferation, maintenance, and differentiation of Wharton's jelly-derived mesenchymal stem cells (WJMSCs) into corneal epithelial cells (CECs).MethodScaffolds loaded with PRGF were evaluated through release studies, cytotoxicity assays, and cell differentiation. The proliferation and differentiation of WJMSCs and Limbal Epithelial Stem Cells (LESCs) were investigated using MTT assays, real-time PCR and immunostaining.ResultsThe PRGF-loaded Co/SF scaffold significantly promoted the proliferation of both WJMSCs and LESCs in a concentration-dependent manner. Real-time PCR and immune staining revealed a significant increase in the expression of P63, ABCG2, and cytokeratin 3/12 markers in WJMSCs, a significant decrease in the expression of P63 and ABCG2, and a significant increase in the expression of cytokeratin 3/12 markers indicating successful differentiation into CECs.ConclusionThe WJMSC cultured on PRGF-enriched Co/SF scaffold demonstrates potential as a viable alternative to conventional CLET, offering a promising strategy for corneal tissue regeneration.
引用
收藏
页码:549 / 560
页数:12
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