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ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE
The CD9 is transmembrane protein that plays a critical role in many cellular processes including aging associated cardiac pathologies. The heart function declines in the aged population. Ageing is strongly associated with many age-related conditions such as increased risk of heart failure. If aging...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845330/ http://dx.doi.org/10.1093/geroni/igz038.953 |
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author | Jonnakuti, Sriya T Ullah, Mujib |
author_facet | Jonnakuti, Sriya T Ullah, Mujib |
author_sort | Jonnakuti, Sriya T |
collection | PubMed |
description | The CD9 is transmembrane protein that plays a critical role in many cellular processes including aging associated cardiac pathologies. The heart function declines in the aged population. Ageing is strongly associated with many age-related conditions such as increased risk of heart failure. If aging can be prevented slowed down or even reversed, heart failure and other signs of aging could be controlled or even cured. It is unknown whether CD9 is cardioprotective. The objective of this study is to investigate whether a decline CD9 levels contributes to aging-related heart failure. Our data shows that CD9-deficient aged mice develop cardiac abnormalities and pathological cardiac hypertrophy, Cardioprotection by CD9 in old mice is followed by the downregulation of SIRT6 in the heart, and CD9 overexpressed exosomes ameliorates cardiac pathologies in treated mice and improves their long-term survival. Additionally, the serum level of CD9 decreased significantly in aged mice. CD9 overexpressed exosomes are cardioprotective and improve cardiac function in aged mice. These exosomes mediate their paracrine effects by attenuating, blood pressure, heart beat, reactive oxygen species and fibrosis. Remarkably, CD9 overexpression reversed fibrosis associated brain natriuretic peptide (BNP), Sirt6, and galectin 3 (Gal-3). These results provide a new perspective on the pathogenesis of cardiomyopathies and open new avenues for treatment of the disease. |
format | Online Article Text |
id | pubmed-6845330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68453302019-11-21 ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE Jonnakuti, Sriya T Ullah, Mujib Innov Aging Session 1310 (Poster) The CD9 is transmembrane protein that plays a critical role in many cellular processes including aging associated cardiac pathologies. The heart function declines in the aged population. Ageing is strongly associated with many age-related conditions such as increased risk of heart failure. If aging can be prevented slowed down or even reversed, heart failure and other signs of aging could be controlled or even cured. It is unknown whether CD9 is cardioprotective. The objective of this study is to investigate whether a decline CD9 levels contributes to aging-related heart failure. Our data shows that CD9-deficient aged mice develop cardiac abnormalities and pathological cardiac hypertrophy, Cardioprotection by CD9 in old mice is followed by the downregulation of SIRT6 in the heart, and CD9 overexpressed exosomes ameliorates cardiac pathologies in treated mice and improves their long-term survival. Additionally, the serum level of CD9 decreased significantly in aged mice. CD9 overexpressed exosomes are cardioprotective and improve cardiac function in aged mice. These exosomes mediate their paracrine effects by attenuating, blood pressure, heart beat, reactive oxygen species and fibrosis. Remarkably, CD9 overexpression reversed fibrosis associated brain natriuretic peptide (BNP), Sirt6, and galectin 3 (Gal-3). These results provide a new perspective on the pathogenesis of cardiomyopathies and open new avenues for treatment of the disease. Oxford University Press 2019-11-08 /pmc/articles/PMC6845330/ http://dx.doi.org/10.1093/geroni/igz038.953 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Session 1310 (Poster) Jonnakuti, Sriya T Ullah, Mujib ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title | ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title_full | ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title_fullStr | ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title_full_unstemmed | ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title_short | ANTI-AGING PROTEIN CD9 AFFECTS AGE-RELATED HEART FAILURE |
title_sort | anti-aging protein cd9 affects age-related heart failure |
topic | Session 1310 (Poster) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845330/ http://dx.doi.org/10.1093/geroni/igz038.953 |
work_keys_str_mv | AT jonnakutisriyat antiagingproteincd9affectsagerelatedheartfailure AT ullahmujib antiagingproteincd9affectsagerelatedheartfailure |