Senescence markers in subcutaneous preadipocytes differ in childhood‐ versus adult‐onset obesity before and after weight loss

Author:

Murphy Jessica123ORCID,Tam Bjorn T.1234ORCID,Kirkland James L.5ORCID,Tchkonia Tamara5ORCID,Giorgadze Nino5,Pirtskhalava Tamar5,Tsoukas Michael A.6ORCID,Morais José A.17ORCID,Santosa Sylvia123ORCID

Affiliation:

1. Department of Health, Kinesiology, and Applied Physiology Concordia University Montréal Québec Canada

2. Metabolism, Obesity, and Nutrition Laboratory, PERFORM Centre Concordia University Montréal Québec Canada

3. Centre de recherche—Axe maladies chroniques, Centre intégré universitaire de santé et de services sociaux du Nord‐de‐l'Ile‐de‐Montréal Hôpital du Sacré‐Coeur de Montréal Montréal Québec Canada

4. Department of Sport, Physical Education, and Health, Faculty of Social Sciences Hong Kong Baptist University Kowloon Tong Hong Kong China

5. Robert and Arlene Kogod Center on Aging Mayo Clinic Rochester Minnesota USA

6. Division of Endocrinology and Metabolism, Department of Medicine McGill University, Royal Victoria Hospital, McGill University Health Centre Glen Site Montréal Québec Canada

7. Division of Geriatric Medicine, Department of Medicine McGill University, McGill University Health Centre‐Montréal General Hospital Montréal Québec Canada

Abstract

AbstractObjectiveThe aim of this study was to determine the effect of age of obesity onset on senescence‐related markers in abdominal (AB) and femoral (FEM) subcutaneous adipose tissue (SAT) before and after moderate (~10%) weight loss.MethodsAB and FEM SAT were collected from human females with childhood‐onset obesity (CO) or adult‐onset obesity (AO) before and after diet‐ and exercise‐induced weight loss. Immunofluorescence analysis of γH2AX/RAD51 (DNA damage/repair markers) and p53/p21 (senescence markers) was conducted in cultured preadipocytes, and senescence‐associated β‐galactosidase (SA‐β‐gal) activity was measured in SAT.ResultsCO had proportionately more AB and FEM preadipocytes with DNA damage (γH2AX+) and senescence markers (p53+ and/or p21+) than AO at baseline. The proportion of γH2AX+ FEM preadipocytes declined with weight loss in CO and was similar between groups after weight loss. The number of γH2AX foci in γH2AX+ preadipocytes decreased similarly between groups and regions with weight loss in parallel with an increase in RAD51. The proportion of p53+ and p21+ preadipocytes and SA‐β‐gal+ cells in SAT did not change with weight loss, but the total p21 intensity in p53+/p21+ FEM preadipocytes declined in AO.ConclusionsThese results provide preliminary evidence that females with CO have an accelerated preadipocyte aging state that improves with weight loss in terms of DNA damage but not senescence.

Funder

Heart and Stroke Foundation of Canada

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)

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