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Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice
Cdc42 is a small RhoGTPase regulating multiple functions in eukaryotic cells. The activity of Cdc42 is significantly elevated in several tissues of aged mice, while the Cdc42 gain‐of‐activity mouse model presents with a premature aging‐like phenotype and with decreased lifespan. These data suggest a...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511875/ https://www.ncbi.nlm.nih.gov/pubmed/32755011 http://dx.doi.org/10.1111/acel.13208 |
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author | Florian, Maria Carolina Leins, Hanna Gobs, Michael Han, Yang Marka, Gina Soller, Karin Vollmer, Angelika Sakk, Vadim Nattamai, Kalpana J. Rayes, Ahmad Zhao, Xueheng Setchell, Kenneth Mulaw, Medhanie Wagner, Wolfgang Zheng, Yi Geiger, Hartmut |
author_facet | Florian, Maria Carolina Leins, Hanna Gobs, Michael Han, Yang Marka, Gina Soller, Karin Vollmer, Angelika Sakk, Vadim Nattamai, Kalpana J. Rayes, Ahmad Zhao, Xueheng Setchell, Kenneth Mulaw, Medhanie Wagner, Wolfgang Zheng, Yi Geiger, Hartmut |
author_sort | Florian, Maria Carolina |
collection | PubMed |
description | Cdc42 is a small RhoGTPase regulating multiple functions in eukaryotic cells. The activity of Cdc42 is significantly elevated in several tissues of aged mice, while the Cdc42 gain‐of‐activity mouse model presents with a premature aging‐like phenotype and with decreased lifespan. These data suggest a causal connection between elevated activity of Cdc42, aging, and reduced lifespan. Here, we demonstrate that systemic treatment of aged (75‐week‐old) female C57BL/6 mice with a Cdc42 activity‐specific inhibitor (CASIN) for 4 consecutive days significantly extends average and maximum lifespan. Moreover, aged CASIN‐treated animals displayed a youthful level of the aging‐associated cytokines IL‐1β, IL‐1α, and INFγ in serum and a significantly younger epigenetic clock as based on DNA methylation levels in blood cells. Overall, our data show that systemic administration of CASIN to reduce Cdc42 activity in aged mice extends murine lifespan. |
format | Online Article Text |
id | pubmed-7511875 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75118752020-09-30 Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice Florian, Maria Carolina Leins, Hanna Gobs, Michael Han, Yang Marka, Gina Soller, Karin Vollmer, Angelika Sakk, Vadim Nattamai, Kalpana J. Rayes, Ahmad Zhao, Xueheng Setchell, Kenneth Mulaw, Medhanie Wagner, Wolfgang Zheng, Yi Geiger, Hartmut Aging Cell Short Take Cdc42 is a small RhoGTPase regulating multiple functions in eukaryotic cells. The activity of Cdc42 is significantly elevated in several tissues of aged mice, while the Cdc42 gain‐of‐activity mouse model presents with a premature aging‐like phenotype and with decreased lifespan. These data suggest a causal connection between elevated activity of Cdc42, aging, and reduced lifespan. Here, we demonstrate that systemic treatment of aged (75‐week‐old) female C57BL/6 mice with a Cdc42 activity‐specific inhibitor (CASIN) for 4 consecutive days significantly extends average and maximum lifespan. Moreover, aged CASIN‐treated animals displayed a youthful level of the aging‐associated cytokines IL‐1β, IL‐1α, and INFγ in serum and a significantly younger epigenetic clock as based on DNA methylation levels in blood cells. Overall, our data show that systemic administration of CASIN to reduce Cdc42 activity in aged mice extends murine lifespan. John Wiley and Sons Inc. 2020-08-04 2020-09 /pmc/articles/PMC7511875/ /pubmed/32755011 http://dx.doi.org/10.1111/acel.13208 Text en © 2020 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Take Florian, Maria Carolina Leins, Hanna Gobs, Michael Han, Yang Marka, Gina Soller, Karin Vollmer, Angelika Sakk, Vadim Nattamai, Kalpana J. Rayes, Ahmad Zhao, Xueheng Setchell, Kenneth Mulaw, Medhanie Wagner, Wolfgang Zheng, Yi Geiger, Hartmut Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title | Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title_full | Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title_fullStr | Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title_full_unstemmed | Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title_short | Inhibition of Cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female C57BL/6 mice |
title_sort | inhibition of cdc42 activity extends lifespan and decreases circulating inflammatory cytokines in aged female c57bl/6 mice |
topic | Short Take |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7511875/ https://www.ncbi.nlm.nih.gov/pubmed/32755011 http://dx.doi.org/10.1111/acel.13208 |
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