| Literature DB >> 32004455 |
Yasuto Takeuchi1, Rika Narumi1, Ryutaro Akiyama2, Elisa Vitiello3, Takanobu Shirai1, Nobuyuki Tanimura1, Keisuke Kuromiya1, Susumu Ishikawa1, Mihoko Kajita1, Masazumi Tada4, Yukinari Haraoka5, Yuki Akieda5, Tohru Ishitani5, Yoichiro Fujioka6, Yusuke Ohba6, Sohei Yamada7, Yoichiroh Hosokawa8, Yusuke Toyama9, Takaaki Matsui10, Yasuyuki Fujita11.
Abstract
When oncogenic transformation or apoptosis occurs within epithelia, the harmful or dead cells are apically extruded from tissues to maintain epithelial homeostasis. However, the underlying molecular mechanism still remains elusive. In this study, we first show, using mammalian cultured epithelial cells and zebrafish embryos, that prior to apical extrusion of RasV12-transformed cells, calcium wave occurs from the transformed cell and propagates across the surrounding cells. The calcium wave then triggers and facilitates the process of extrusion. IP3 receptor, gap junction, and mechanosensitive calcium channel TRPC1 are involved in calcium wave. Calcium wave induces the polarized movement of the surrounding cells toward the extruding transformed cells. Furthermore, calcium wave facilitates apical extrusion, at least partly, by inducing actin rearrangement in the surrounding cells. Moreover, comparable calcium propagation also promotes apical extrusion of apoptotic cells. Thus, calcium wave is an evolutionarily conserved, general regulatory mechanism of cell extrusion.Entities:
Keywords: INF2; RasV12-transformed; TRPC1; actin rearrangement; apoptosis; calcium wave; cell extrusion; epithelial homeostasis
Year: 2020 PMID: 32004455 DOI: 10.1016/j.cub.2019.11.089
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834