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c-Met as a new marker of cellular senescence
Author(s) -
Maria Boichuck,
Jonathan Zorea,
Moshe Elkabets,
Marina Wolfson,
Vadim E. Fraifeld
Publication year - 2019
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.101961
Subject(s) - senescence , phenotype , proinflammatory cytokine , stat3 , protein kinase b , apoptosis , microbiology and biotechnology , biology , cellular senescence , signal transduction , cancer research , immunology , genetics , gene , inflammation
Here, we reported for the first time an increased expression of c-Met protein in primary cultures of human dermal and pulmonary fibroblasts of late passages. This suggests that c-Met could serve as an early marker of cellular senescence (CS). The levels of c-Met-related signaling proteins phospho-Akt and Stat3 were also increased in (pre)senescent fibroblasts. Considering the anti-apoptotic activity of Akt and the involvement of Stat3 in mediating the effects of proinflammatory cytokines, the findings of this study indicate that c-Met could contribute through its downstream targets or partners to at least two major phenotypical features of CS - resistance to apoptosis and senescence-associated secretory phenotype.

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