0415 : CD28 deletion improves obesity-induced liver steatosis but increases adiposity in mice

Abstract

Lymphocytes play a critical role in visceral adipose tissue inflammation. The CD28 costimulatory molecule is required for lymphocyte activation and for the development of a functional regulatory T cells (Treg) compartment; however its role during obesity is unknown. During diet-induced obesity, we investigated the effects of selective interference with CD28 signaling using knock-out mice (Cd28KO) and a CTLA4-Ig fusion protein inhibiting CD28-B7 interactions. Cd28 deficiency decreased pathogenic T-cells and Treg content within adipose tissue without changing macrophages number. Cd28KO epididymal but not subcutaneous fat was characterized by enlarged adipocytes, reduced levels of inflammatory cytokines and increased Glut4, adiponectin and lipogenic enzymes mRNA levels. This was associated with reduced inflammation, fat accumulation and enhanced glucose metabolism in liver. Weight gain and fasting glucose tolerance were not affected. CTLA4-Ig injections reduced the number T-cells in epididymal adipose tissue but not inflammatory cytokines levels and failed to improve liver fat accumulation. Deletion of CD28 creates a new pro/anti-inflammatory balance in epididymal adipose tissue and liver and exerts a protective effect against hepatic steatosis.