Essential Role of Adhesion GPCR, GPR123, for Human Pluripotent Stem Cells and Reprogramming towards Pluripotency

• Published in: Cells (Basel, Switzerland) Vol. 12; no. 2; p. 304
• Main Authors: Krasnova, Olga A, Kulakova, Karina A, Sopova, Julia V, Smirnov, Evgenyi Y, Silonov, Sergey A, Lomert, Ekaterina V, Bystrova, Olga A, Martynova, Marina G, Neganova, Irina E
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13-01-2023; MDPI
• Subjects: Actin; adhesion GPCRs; Antibodies; Cell cycle; Cell Differentiation - genetics; Cell surface; Cellular Reprogramming; Colonies; Cytology; Cytoskeleton; E-cadherin; Embryogenesis; Fibroblasts; G protein-coupled receptors; G proteins; G2 phase; GPCRs; human pluripotent stem cells; Humans; Induced Pluripotent Stem Cells - metabolism; Kinases; Microscopy; Phosphatase; Pluripotency; Pluripotent Stem Cells - metabolism; Proteins; Receptors, G-Protein-Coupled - genetics; Receptors, G-Protein-Coupled - metabolism; reprogramming; RNA-mediated interference; Software; Stem cells; Netherlands; United Kingdom > UK; United States > US; Japan; reprogramming; adhesion GPCRs; GPCRs; G proteins; human pluripotent stem cells; pluripotency; GPR123
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12020304

G-protein-coupled receptors (GPCRs) are the largest family of cell surface receptors. They modulate key physiological functions and are required in diverse developmental processes including embryogenesis, but their role in pluripotency maintenance and acquisition during the reprogramming towards hiPSCs draws little attention. Meanwhile, it is known that more than 106 GPCRs are overexpressed in human pluripotent stem cells (hPSCs). Previously, to identify novel effectors of reprogramming, we performed a high-throughput RNA interference (RNAi) screening assay and identified adhesion GPCR, GPR123, as a potential reprogramming effector. Its role has not been explored before. Herein, by employing
RNAi we addressed the role of GPR123 for hPSCs. The suppression of
in hPSCs leads to the loss of pluripotency and differentiation, impacted colony morphology, accumulation of cells at the G2 phase of the cell cycle, and absence of the scratch closure. Application of the
RNAi at the initiation stage of reprogramming leads to a decrease in the percentage of the "true" hiPSC colonies, a drop in E-cadherin expression, a decrease in the percentage of NANOG+ nuclei, and the absence of actin cytoskeleton remodeling. Together this leads to the absence of the alkaline-phosphatase-positive hiPSCs colonies on the 18th day of the reprogramming process. Overall, these data indicate for the first time the essential role of GPR123 in the maintenance and acquisition of pluripotency.