| Literature DB >> 29417866 |
Yuyao Wang1,2, Dandan Zhang1,2, Yi Zhang1,2, Ni Ni1,2, Zhimin Tang1,2, Zhisha Bai3, Bingqiao Shen1,2, Hao Sun1,2, Ping Gu1,2.
Abstract
Strategies to improve retinal progenitor cell (RPC) capacity to yield proliferative and multipotent pools of cells that can efficiently differentiate into retinal neurons, including photoreceptors, could be vital for cell therapy in retinal degenerative diseases. In this study, we found that insulin-like growth factor-1 (IGF-1) plays a role in the regulation of proliferation and differentiation of RPCs. Our results show that IGF-1 promotes RPC proliferation via IGF-1 receptors (IGF-1Rs), stimulating increased phosphorylation in the PI3K/Akt and MAPK/Erk pathways. An inhibitor experiment revealed that IGF-1-induced RPC proliferation was inhibited when the PI3K/Akt and MAPK/Erk pathways were blocked. Furthermore, under the condition of differentiation, IGF-1-pretreated RPCs prefer to differentiate into retinal neurons, including photoreceptors, in vitro, which is crucial for visual formation and visual restoration. These results demonstrate that IGF-1 accelerates the proliferation of RPCs and IGF-1 pretreated RPCs may have shown an increased potential for retinal neuron differentiation, providing a novel strategy for regulating the proliferation and differentiation of retinal progenitors in vitro and shedding light upon the application of RPCs in retinal cell therapy.Entities:
Keywords: Retinal progenitor cell (RPC); differentiation; insulin-like growth factor-1 (IGF-1); proliferation; signal pathway
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Year: 2018 PMID: 29417866 PMCID: PMC5927662 DOI: 10.1080/15384101.2018.1431594
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534