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c-Met as a new marker of cellular senescence

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-Ak...

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Autores principales: Boichuck, Maria, Zorea, Jonathan, Elkabets, Moshe, Wolfson, Marina, Fraifeld, Vadim E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535066/
https://www.ncbi.nlm.nih.gov/pubmed/31085799
http://dx.doi.org/10.18632/aging.101961
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author Boichuck, Maria
Zorea, Jonathan
Elkabets, Moshe
Wolfson, Marina
Fraifeld, Vadim E.
author_facet Boichuck, Maria
Zorea, Jonathan
Elkabets, Moshe
Wolfson, Marina
Fraifeld, Vadim E.
author_sort Boichuck, Maria
collection PubMed
description 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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spelling pubmed-65350662019-06-04 c-Met as a new marker of cellular senescence Boichuck, Maria Zorea, Jonathan Elkabets, Moshe Wolfson, Marina Fraifeld, Vadim E. Aging (Albany NY) Research Paper 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. Impact Journals 2019-05-13 /pmc/articles/PMC6535066/ /pubmed/31085799 http://dx.doi.org/10.18632/aging.101961 Text en Copyright © 2019 Boichuck et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Boichuck, Maria
Zorea, Jonathan
Elkabets, Moshe
Wolfson, Marina
Fraifeld, Vadim E.
c-Met as a new marker of cellular senescence
title c-Met as a new marker of cellular senescence
title_full c-Met as a new marker of cellular senescence
title_fullStr c-Met as a new marker of cellular senescence
title_full_unstemmed c-Met as a new marker of cellular senescence
title_short c-Met as a new marker of cellular senescence
title_sort c-met as a new marker of cellular senescence
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535066/
https://www.ncbi.nlm.nih.gov/pubmed/31085799
http://dx.doi.org/10.18632/aging.101961
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