Electrospun SF/PLCL nanofibrous membrane: a potential scaffold for retinal progenitor cell proliferation and differentiation

被引:0
作者
Dandan Zhang
Ni Ni
Junzhao Chen
Qinke Yao
Bingqiao Shen
Yi Zhang
Mengyu Zhu
Zi Wang
Jing Ruan
Jing Wang
Xiumei Mo
Wodong Shi
Jing Ji
Xianqun Fan
Ping Gu
机构
[1] Ninth People's Hospital,Department of Ophthalmology
[2] Shanghai Jiao Tong University School of Medicine,Biomaterials and Tissue Engineering Laboratory, College of Chemistry & Chemical Engineering and Biotechnology
[3] Donghua University,undefined
来源
Scientific Reports | / 5卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Biocompatible polymer scaffolds are promising as potential carriers for the delivery of retinal progenitor cells (RPCs) in cell replacement therapy for the repair of damaged or diseased retinas. The primary goal of the present study was to investigate the effects of blended electrospun nanofibrous membranes of silk fibroin (SF) and poly(L-lactic acid-co-ε-caprolactone) (PLCL), a novel scaffold, on the biological behaviour of RPCs in vitro. To assess the cell-scaffold interaction, RPCs were cultured on SF/PLCL scaffolds for indicated durations. Our data revealed that all the SF/PLCL scaffolds were thoroughly cytocompatible and the SF:PLCL (1:1) scaffolds yielded the best RPC growth. The in vitro proliferation assays showed that RPCs proliferated more quickly on the SF:PLCL (1:1) than on the other scaffolds and the control. Quantitative polymerase chain reaction (qPCR) and immunocytochemistry analyses demonstrated that RPCs grown on the SF:PLCL (1:1) scaffolds preferentially differentiated toward retinal neurons, including, most interestingly, photoreceptors. In summary, we demonstrated that the SF:PLCL (1:1) scaffolds can not only markedly promote RPC proliferation with cytocompatibility for RPC growth but also robustly enhance RPCs’ differentiation toward specific retinal neurons of interest in vitro, suggesting that SF:PLCL (1:1) scaffolds may have potential applications in retinal cell replacement therapy in the future.
引用
收藏
相关论文
共 110 条
[1]  
Margalit E(2003)Retinal and optic nerve diseases Artif Organs 27 963-974
[2]  
Sadda SR(2011)Surgical approaches to gene and stem cell therapy for retinal disease Hum Gene Ther 22 531-535
[3]  
Stout JT(2004)Stem cells and retinal repair Prog Retin Eye Res 23 149-181
[4]  
Francis PJ(2004)Multipotent retinal progenitors express developmental markers, differentiate into retinal neurons and preserve light-mediated behavior Invest Ophthalmol Vis Sci 45 4167-4173
[5]  
Klassen H(2007)Isolation of retinal progenitor and stem cells from the porcine eye Mol Vis 13 1045-1057
[6]  
Sakaguchi DS(2009)Sequential changes in the gene expression profile of murine retinal progenitor cells during the induction of differentiation Mol Vis 15 2111-2122
[7]  
Young MJ(2012)An Brain Res 1433 38-46
[8]  
Klassen HJ(2000) comparison of two different subpopulations of retinal progenitor cells for self-renewal and multipotentiality Science (New York, NY) 287 2032-2036
[9]  
Gu P(2005)Retinal stem cells in the adult mammalian eye Stem cells (Dayton, Ohio) 23 424-432
[10]  
Gu P(2014)Effects of ciliary neurotrophic factor on differentiation of late retinal progenitor cells Tissue Eng Part A 20 1465-1475