Increased insulin sensitivity despite lipodystrophy in Crebbp heterozygous mice

The CBP protein (cAMP response element binding protein (CREB) binding protein)(1) is a co-activator(2) for several transcription factors with a wide range of important biological functions, such as sterol regulatory element binding proteins (SREBPs)(3), CCAAT/enhancer-binding proteins (C/EBPs)(4), nuclear receptors(5,6) (including peroxisome proliferator-activated receptors, PPARS)(7), and signal transducers and activators of transcription (STATs)(8). In contrast to these individual transcription factors, the biological roles of CBP are poorly understood. CBP enhances transcriptional activities via histone acetylation and the recruitment of additional co-activators such as SRC (steroid coactivator)-1 (ref. 9). To identify its physiological functions using a loss-of-function mutant, we analyzed CBP-deficient mice(10-12). As Crebbp null mice (Crebbp(-/-)) died during embryogenesis(10-12), we used Crebbp(+/-) mice(12). Unexpectedly, Crebbp(+/-) mice showed markedly reduced weight of white adipose tissue (WAT) but not of other tissues. Despite this lipodystrophy, Crebbp(+/-) mice showed increased insulin sensitivity and glucose tolerance and were completely protected from body weight gain induced by a high-fat (HF) diet. We observed increased leptin sensitivity and increased serum adiponectin levels in Crebbp(+/-) mice. These increased effects of insulin-sensitizing hormones secreted from WAT may explain, at least in part, the phenotypes of Crebbp(+/-) mice. This study demonstrates that CBP may function as a 'master-switch' between energy storage and expenditure.