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Prostaglandin E(2) and its receptor EP2 trigger signaling that contributes to YAP‐mediated cell competition

Cell competition is a biological process by which unfit cells are eliminated from “cell society.” We previously showed that cultured mammalian epithelial Madin‐Darby canine kidney (MDCK) cells expressing constitutively active YAP were eliminated by apical extrusion when surrounded by “normal” MDCK c...

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Detalles Bibliográficos
Autores principales: Ishihara, Erika, Nagaoka, Yuya, Okuno, Toshiaki, Kofuji, Satoshi, Ishigami‐Yuasa, Mari, Kagechika, Hiroyuki, Kamimura, Kenya, Terai, Shuji, Yokomizo, Takehiko, Sugimoto, Yukihiko, Fujita, Yasuyuki, Suzuki, Akira, Nishina, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7078805/
https://www.ncbi.nlm.nih.gov/pubmed/31989743
http://dx.doi.org/10.1111/gtc.12750
Descripción
Sumario:Cell competition is a biological process by which unfit cells are eliminated from “cell society.” We previously showed that cultured mammalian epithelial Madin‐Darby canine kidney (MDCK) cells expressing constitutively active YAP were eliminated by apical extrusion when surrounded by “normal” MDCK cells. However, the molecular mechanism underlying the elimination of active YAP‐expressing cells was unknown. Here, we used high‐throughput chemical compound screening to identify cyclooxygenase‐2 (COX‐2) as a key molecule triggering cell competition. Our work shows that COX‐2‐mediated PGE(2) secretion engages its receptor EP2 on abnormal and nearby normal cells. This engagement of EP2 triggers downstream signaling via an adenylyl cyclase‐cyclic AMP‐PKA pathway that, in the presence of active YAP, induces E‐cadherin internalization leading to apical extrusion. Thus, COX‐2‐induced PGE(2) appears a warning signal to both abnormal and surrounding normal cells to drive cell competition.