YWK-II protein as a novel G(o)-coupled receptor for Müllerian inhibiting substance in cell survival.

J Cell Sci

National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, 5 Dong Dan San Tiao, Beijing 100005, China.

Published: May 2007

AI Article Synopsis

  • The study investigates Müllerian inhibiting substance (MIS) and its role in promoting cell survival, focusing on the YWK-II protein as a potential receptor involved in this process.
  • In CHO cells overexpressing YWK-II, MIS activates the G(o)-coupled ERK1/2 signaling pathway, enhancing cell survival while altering levels of p53 and caspase-3.
  • In vivo experiments with a YWK-II antibody in mice suggest that inhibiting YWK-II decreases sperm count and increases markers of apoptosis, supporting the idea that YWK-II mediates MIS's protective effects on cells.

Article Abstract

Müllerian inhibiting substance (MIS) has recently been implicated in multiple cellular functions including promotion of cell survival, but the receptor(s) and signaling pathways involved remain elusive. We have investigated the possibility of YWK-II protein, previously shown to interact physically with MIS and G(o) protein, being a receptor mediating the cell survival effect of MIS. In YWK-II-overexpressing CHO cells, MIS activates the G(o)-coupled ERK1/2 signaling pathway and promotes cell survival with altered levels of p53 and caspase-3. YWK-II antibody is found to interfere with the ability of MIS to promote viability of mouse sperm and affect MIS-activated ERK1/2 phosphorylation. In vivo studies involving injection of YWK-II antibody into the seminiferous tubule of the mouse testis, where MIS is known to be produced, show significant reduction in the sperm count with accumulation of p53 and cleaved caspase-3 in testicular nuclei. Taken together, the present study has demonstrated a new G(o)-coupled receptor for MIS in mediating ERK1/2 activation leading to anti-apoptotic activity or cell survival.

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Source
http://dx.doi.org/10.1242/jcs.001230DOI Listing

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