CTRP3 deficiency reduces liver size and alters IL-6 and TGFβ levels in obese mice

• Published in: American journal of physiology: endocrinology and metabolism Vol. 310; no. 5; p. E332
• Main Authors: Wolf, Risa M, Lei, Xia, Yang, Zhi-Chun, Nyandjo, Maeva, Tan, Stefanie Y, Wong, G William
• Format: Journal Article
• Language: English
• Published: United States 01-03-2016
• Subjects: Adipokines - genetics; Adipose Tissue; Animals; Calorimetry, Indirect; Chemokine CCL2 - genetics; Diacylglycerol O-Acyltransferase - genetics; Diet, Fat-Restricted; Diet, High-Fat; Female; Gluconeogenesis - genetics; Glucose - metabolism; Glucose Tolerance Test; Glycerol-3-Phosphate O-Acyltransferase - genetics; Inflammation; Insulin Resistance - genetics; Interleukin-6 - metabolism; Lipid Metabolism - genetics; Liver - metabolism; Liver - pathology; Male; Matrix Metalloproteinase 12 - genetics; Mice; Mice, Knockout; Obesity - genetics; Obesity - metabolism; Obesity - pathology; Organ Size; Oxidation-Reduction; Real-Time Polymerase Chain Reaction; Reverse Transcriptase Polymerase Chain Reaction; Transcriptome; Transforming Growth Factor beta1 - metabolism; Tumor Necrosis Factor-alpha - genetics; Weight Gain - genetics; fatty liver; C1q/tumor necrosis factor-related protein; adipokine; diabetes; C1q/tumor necrosis factor; obesity
• ISSN: 1522-1555
• DOI: 10.1152/ajpendo.00248.2015

C1q/TNF-related protein 3 (CTRP3) is a secreted metabolic regulator whose circulating levels are reduced in human and rodent models of obesity and diabetes. Previously, we showed that CTRP3 infusion lowers blood glucose by suppressing gluconeogenesis and that transgenic overexpression of CTRP3 protects mice against diet-induced hepatic steatosis. Here, we used a genetic loss-of-function mouse model to further address whether CTRP3 is indeed required for metabolic homeostasis under normal and obese states. Both male and female mice lacking CTRP3 had similar weight gain when fed a control low-fat (LFD) or high-fat diet (HFD). Regardless of diet, no differences were observed in adiposity, food intake, metabolic rate, energy expenditure, or physical activity levels between wild-type (WT) and Ctrp3-knockout (KO) animals of either sex. Contrary to expectations, loss of CTRP3 in LFD- or HFD-fed male and female mice also had minimal or no impact on whole body glucose metabolism, insulin sensitivity, and fasting-induced hepatic gluconeogenesis. Unexpectedly, the liver sizes of HFD-fed Ctrp3-KO male mice were markedly reduced despite a modest increase in triglyceride content. Furthermore, liver expression of fat oxidation genes was upregulated in the Ctrp3-KO mice. Whereas the liver and adipose expression of profibrotic TGFβ1, as well as its serum levels, was suppressed in HFD-fed KO mice, circulating proinflammatory IL-6 levels were markedly increased; these changes, however, were insufficient to affect systemic metabolic outcome. We conclude that, although it is dispensable for physiological control of energy balance, CTRP3 plays a previously unsuspected role in modulating liver size and circulating cytokine levels in response to obesity.