4.5 Article

Sex Differences in Inflammatory Responses to Adipose Tissue Lipolysis in Diet-Induced Obesity

期刊

ENDOCRINOLOGY
卷 160, 期 2, 页码 293-312

出版社

ENDOCRINE SOC
DOI: 10.1210/en.2018-00797

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资金

  1. Pediatrics Elizabeth E. Kennedy Children's Research Award
  2. Claude D. Pepper Older Americans Independence Center/Michigan Biology of Cardiovascular Aging pilot award (National Instituteon Aging Grant) [AG024824/UL1TR002240]
  3. National Institutes of Health/National Institute of Diabetes and Digestive and Kidney Diseases [K08DK101755, R01 DK115583]
  4. Edith Briskin/SKS Foundation Taubman Emerging Scholar support
  5. National Institutes of Health [DK089503]

向作者/读者索取更多资源

Males are known to have profound adipose tissue macrophage (ATM) accumulation in gonadal white adipose tissue (GWAT) during obesity, whereas females are protected from such an inflammatory response even with increased adiposity. The inflammatory tone in males is linked to insulin resistance and might be the underlying cause for sex differences in metabolic disease. Factors regulating the meta-inflammatory response remain unclear but enhanced lipid storage in females may explain the reduced inflammatory response to high-fat diets. In this study, we evaluated lean and obese females with stimulated lipolysis to understand whether a stress release of free fatty acids (FFAs) could induce female ATMs. We demonstrate that in both lean and obese females, GWAT CD11c(-) resident ATMs accumulate with beta-3 adrenergic receptor-stimulated lipolysis. Lipolysis elevated serum FFA, triglyceride, and IL-6 levels in females that corresponded to significant phosphorylated hormone-sensitive lipase and adipose triglyceride lipase protein expression in obese female GWAT compared with males. Increased lipolytic response in obese females was associated with crown-like structures and induced Il6, Mcp1, Arg1, and Mgl1 expression in obese female GWAT, suggesting an environment of lipid clearance and adipose remodeling. With this finding we next investigated whether lipid storage and lipolytic mediators differed by sex. Diacylglycerol, ceramides, phospholipids, and certain fatty acid species associated with inflammation were elevated in male GWAT compared with obese female GWAT. Overall, our data demonstrate a role for GWAT lipid storage and lipolytic metabolites to induce inflammation in males and induce remodeling in females that might explain sex differences in overall metabolic health.

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