Li Guilan, Liu Sheng, Chen Wenfei, Jiang Zhijian, Luo Yuanting, Wang Dongliang, Zheng Yingfeng, Liu Yizhi
Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, #7 Jinsui Road, Tianhe District, Guangzhou, 510060, China.
Research Unit of Ocular Development and Regeneration, Chinese Academy of Medical Sciences, Beijing, 100730, China.
Adv Healthc Mater. 2022 Dec;11(23):e2202114. doi: 10.1002/adhm.202202114. Epub 2022 Oct 17.
Replenishing the retina with retinal pigment epithelial (RPE) cells derived from pluripotent stem cells (PSCs) has great promise for treating retinal degenerative diseases, but it is limited by poor cell survival and integration in vivo. Herein, porcine acellular sclera and uvea extracellular matrix (ECM) and their counterpart hydrogels are developed, and their effects on the biological behavior of human induced pluripotent stem cell (hiPSC)-derived RPE cells (hiPSC-RPE) and embryoid body (hiPSC-EB) differentiation are investigated. Both acellular ECM hydrogels have excellent biocompatibility and suitable biodegradability without evoking an obvious immune response. Most importantly, the decellularized uvea hydrogel-delivered cells' injection remarkably promotes the hiPSC-RPE cells' survival and integration in the subretinal space, rescues the photoreceptor cells' death and retinal gliosis, and restores vision in rats with retinal degeneration for a long duration. In addition, medium supplementation with decellularized uvea peptides promotes hiPSC-EBs onset morphogenesis and neural/retinal differentiation, forming layered retinal organoids. This study demonstrates that ECM hydrogel-delivered hiPSC-RPE cells' injection may be a useful approach for treating retinal degeneration disease, combined with an optimized retinal seeding cells' induction program, which has potential for clinical application.
用多能干细胞(PSC)来源的视网膜色素上皮(RPE)细胞补充视网膜对治疗视网膜退行性疾病具有巨大潜力,但受限于细胞在体内的低存活率和整合能力。在此,制备了猪脱细胞巩膜和葡萄膜细胞外基质(ECM)及其对应的水凝胶,并研究了它们对人诱导多能干细胞(hiPSC)来源的RPE细胞(hiPSC-RPE)生物学行为和胚状体(hiPSC-EB)分化的影响。两种脱细胞ECM水凝胶均具有优异的生物相容性和合适的生物降解性,且不会引发明显的免疫反应。最重要的是,经脱细胞葡萄膜水凝胶递送细胞的注射显著促进了hiPSC-RPE细胞在视网膜下间隙的存活和整合,挽救了光感受器细胞的死亡和视网膜胶质增生,并长期恢复了视网膜变性大鼠的视力。此外,添加脱细胞葡萄膜肽的培养基可促进hiPSC-EB的起始形态发生和神经/视网膜分化,形成分层的视网膜类器官。本研究表明,经ECM水凝胶递送hiPSC-RPE细胞的注射结合优化的视网膜接种细胞诱导方案可能是治疗视网膜变性疾病的一种有效方法,具有临床应用潜力。