Aged-senescent cells contribute to impaired heart regeneration.

aging cardiac regeneration cardiac repair myocardial infarction p16INK4a progenitor cells senescence senescence-associated secretory phenotype senolytics

Journal

Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839

Informations de publication

Date de publication:
06 2019
Historique:
received: 19 10 2018
revised: 09 01 2019
accepted: 31 01 2019
pubmed: 12 3 2019
medline: 15 9 2020
entrez: 12 3 2019
Statut: ppublish

Résumé

Aging leads to increased cellular senescence and is associated with decreased potency of tissue-specific stem/progenitor cells. Here, we have done an extensive analysis of cardiac progenitor cells (CPCs) isolated from human subjects with cardiovascular disease, aged 32-86 years. In aged subjects (>70 years old), over half of CPCs are senescent (p16

Identifiants

pubmed: 30854802
doi: 10.1111/acel.12931
pmc: PMC6516154
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e12931

Subventions

Organisme : Robert J. and Theresa W. Ryan
Pays : International
Organisme : NIA NIH HHS
ID : R37 AG013925
Pays : United States
Organisme : Noaber Foundation
Pays : International
Organisme : British Heart Foundation
ID : PG/14/11/30657
Pays : United Kingdom
Organisme : Glenn/American Federation for Aging Research (AFAR) BIG Award
Pays : International
Organisme : Medical Research Council
ID : MR/P026508/1
Pays : United Kingdom
Organisme : Italian Ministry of Health
ID : GR-2010-2318945
Pays : International
Organisme : NIA NIH HHS
ID : R01 AG013925
Pays : United States
Organisme : Robert and Arlene Kogod
Pays : International
Organisme : The Connor group
Pays : International

Informations de copyright

© 2019 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd.

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Auteurs

Fiona C Lewis-McDougall (FC)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

Prashant J Ruchaya (PJ)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

Eva Domenjo-Vila (E)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

Tze Shin Teoh (T)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

Larissa Prata (L)

Robert and Arlene Kogod Center on Aging, Mayo Clinic College of Medicine, Rochester, Minnesota.

Beverley J Cottle (BJ)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

James E Clark (JE)

School of Cardiovascular Medicine & Sciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

Prakash P Punjabi (PP)

National Heart and Lung Institute, Imperial College London, London, UK.

Wael Awad (W)

Barts Health NHS Trust, London, UK.

Daniele Torella (D)

Molecular and Cellular Cardiology, Department of Medical and Surgical Sciences, Magna Graecia University, Catanzaro, Italy.

Tamara Tchkonia (T)

Robert and Arlene Kogod Center on Aging, Mayo Clinic College of Medicine, Rochester, Minnesota.

James L Kirkland (JL)

Robert and Arlene Kogod Center on Aging, Mayo Clinic College of Medicine, Rochester, Minnesota.

Georgina M Ellison-Hughes (GM)

School of Basic and Medical Biosciences, Faculty of Life Sciences & Medicine, Kings College London, London, UK.

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