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Merck
CN
  • Conserved and novel functions of programmed cellular senescence during vertebrate development.

Conserved and novel functions of programmed cellular senescence during vertebrate development.

Development (Cambridge, England) (2016-11-27)
Hongorzul Davaapil, Jeremy P Brockes, Maximina H Yun
摘要

Cellular senescence, a form of stable cell cycle arrest that is traditionally associated with tumour suppression, has been recently found to occur during mammalian development. Here, we show that cell senescence is an intrinsic part of the developmental programme in amphibians. Programmed senescence occurs in specific structures during defined time windows during amphibian development. It contributes to the physiological degeneration of the amphibian pronephros and to the development of the cement gland and oral cavity. In both contexts, senescence depends on TGFβ but is independent of ERK/MAPK activation. Furthermore, elimination of senescent cells through temporary TGFβ inhibition leads to developmental defects. Our findings uncover conserved and new roles of senescence in vertebrate organogenesis and support the view that cellular senescence may have arisen in evolution as a developmental mechanism.

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Anti-c-Myc抗体,小鼠单克隆 小鼠抗, clone 9E10, purified from hybridoma cell culture
Sigma-Aldrich
抗 MAP 激酶,活化(二磷酸化 ERK-1&2)抗体,小鼠单克隆, clone MAPK-YT, purified from hybridoma cell culture