Exercise Rescues Gene Pathways Involved in Vascular Expansion and Promotes Functional Angiogenesis in Subcutaneous White Adipose Tissue
Authors
Min, So YunLearnard, Heather
Kant, Shashi
Gaelikman, Olga
Rojas-Rodriguez, Raziel
DeSouza, Tiffany
Desai, Anand
Keaney, John F. Jr.
Corvera, Silvia
Craige, Siobhan M.
UMass Chan Affiliations
Graduate School of Biomedical SciencesDivision of Cardiovascular Medicine, Department of Medicine
Program in Molecular Medicine
Document Type
Journal ArticlePublication Date
2019-04-25Keywords
adipose tissueangiogenesis
exercise
glucose homeostasis
high-fat diet
metabolism
Biochemical Phenomena, Metabolism, and Nutrition
Cellular and Molecular Physiology
Exercise Physiology
Exercise Science
Genetic Phenomena
Molecular Biology
Nutritional and Metabolic Diseases
Pathological Conditions, Signs and Symptoms
Tissues
Metadata
Show full item recordAbstract
Exercise mitigates chronic diseases such as diabetes, cardiovascular diseases, and obesity; however, the molecular mechanisms governing protection from these diseases are not completely understood. Here we demonstrate that exercise rescues metabolically compromised high fat diet (HFD) fed mice, and reprograms subcutaneous white adipose tissue (scWAT). Using transcriptomic profiling, scWAT was analyzed for HFD gene expression changes that were rescued by exercise. Gene networks involved in vascularization were identified as prominent targets of exercise, which led us to investigate the vasculature architecture and endothelial phenotype. Vascular density in scWAT was found to be compromised in HFD, and exercise rescued this defect. Similarly, angiogenic capacity as measured by ex vivo capillary sprouting was significantly promoted with exercise. Together, these data demonstrate that exercise enhances scWAT vascularization and functional capacity for angiogenesis, and can prevent the detrimental effects of HFD. The improvement in these indices correlates with improvement of whole-body metabolism, suggesting that scWAT vascularization may be a potential therapeutic target for metabolic disease.Source
Int J Mol Sci. 2019 Apr 25;20(8):2046. pii: ijms20082046. doi: 10.3390/ijms20082046. Link to article on publisher's site
DOI
10.3390/ijms20082046Permanent Link to this Item
http://hdl.handle.net/20.500.14038/41037PubMed ID
31027261Related Resources
Rights
Copyright © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).Distribution License
http://creativecommons.org/licenses/by/4.0/ae974a485f413a2113503eed53cd6c53
10.3390/ijms20082046
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Except where otherwise noted, this item's license is described as Copyright © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).

