Intercellular Adhesion-Dependent Cell Survival and ROCK-Regulated Actomyosin-Driven Forces Mediate Self-Formation of a Retinal Organoid
Year: 2016
Type: article
Abstract: In this study we dissected retinal organoid morphogenesis in human embryonic stem cell (hESC)-derived cultures and established a convenient method for isolating large quantities of retinal organoids for modeling human retinal development and disease. Epithelialized cysts were generated via floating culture of clumps of Matrigel/hESCs. Upon spontaneous attachment and spreading of the cysts, patterned retinal monolayers with tight junctions formed. Dispase-mediated detachment of the monolayers and subsequent floating culture led to self-formation of retinal organoids comprising patterned neuroretina, ciliary margin, and retinal pigment epithelium. Intercellular adhesion-dependent cell survival and ROCK-regulated actomyosin-driven forces are required for the self-organization. Our data supports a hypothesis that newly specified neuroretina progenitors form characteristic structures in equilibrium through minimization of cell surface tension. In long-term culture, the retinal organoids autonomously generated stratified retinal tissues, including photoreceptors with ultrastructure of outer segments. Our system requires minimal manual manipulation, has been validated in two lines of human pluripotent stem cells, and provides insight into optic cup invagination in vivo.
Source: Stem Cell Reports
Institution: Albert Einstein College of Medicine
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $4,190
Awards: G1388498027, G1511159053, Efficient Differentiation of Retinal Pigment Epithelial Cells from hESC, Differentiation of Human ES and iPS Cells into Lens Cells, Developmental regulation of lens gene expression, G6445760679, Training Program in Cellular and Molecular Biology and Genetics, G7908846667, G8095092490, Medical Scientist Training Program, Bronx-Einstein Training in Teaching and Research (BETTR), an IRACDA program, Pax6 as a key regulator of lens development, Gene regulation of retinal cell differentiation
OpenAlex ID: W2343783580
