2012
DOI: 10.1007/s10517-012-1566-2
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In Vitro Histogenesis of Human Embryonic Stem Cells into Retina Components

Abstract: We developed a protocol of in vitro differentiation of human embryonic stem cells into three-dimensional structures histologically and molecularly similar to the developing retina.

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Cited by 3 publications
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“…Insignificant amounts of retinal pigment epithelial cells can be formed during spontaneous differentiation of human pluripotent stem cells [35]. If FGF2, which is necessary to maintain the pluripotent state in culture, is removed from the culture medium, human pluripotent stem cells cultured on a mouse embryonic fibroblast substrate, matrigel, polylysine, or laminin become capable of forming pigment epithelial cells [35, 42, 43]. After 10–12 weeks of spontaneous differentiation, small pigmented regions form, which are then mechanically separated from the rest of the cell mass, yielding an almost pure cell culture of pigment epithelium ( > 99% purity).…”
Section: Directed Differentiation Of Pscs Into Rpementioning
confidence: 99%
“…Insignificant amounts of retinal pigment epithelial cells can be formed during spontaneous differentiation of human pluripotent stem cells [35]. If FGF2, which is necessary to maintain the pluripotent state in culture, is removed from the culture medium, human pluripotent stem cells cultured on a mouse embryonic fibroblast substrate, matrigel, polylysine, or laminin become capable of forming pigment epithelial cells [35, 42, 43]. After 10–12 weeks of spontaneous differentiation, small pigmented regions form, which are then mechanically separated from the rest of the cell mass, yielding an almost pure cell culture of pigment epithelium ( > 99% purity).…”
Section: Directed Differentiation Of Pscs Into Rpementioning
confidence: 99%