Disclosure: The authors declared no conflict of interest.
Version of Record online: 25 MAY 2013
Copyright © 2012 The Obesity Society
Volume 21, Issue 4, pages 737–747, April 2013
How to Cite
S. Purohit, J., Hu, P., Burke, S. J., Collier, J. J., Chen, J. and Zhao, L. (2013), The effects of NOD activation on adipocyte differentiation. Obesity, 21: 737–747. doi: 10.1002/oby.20275
See the online ICMJE Conflict of Interest Forms for this article.
- Issue online: 25 MAY 2013
- Version of Record online: 25 MAY 2013
- Manuscript Accepted: 16 MAY 2012
- Manuscript Received: 29 NOV 2011
Obesity is associated with chronic inflammation. Toll-like receptors (TLR) and NOD-like receptors (NLR) are two families of pattern recognition receptors that play important roles in immune response and inflammation in adipocytes. It has been reported that TLR4 and TLR2 activation induce proinflammatory changes that impair adipocyte differentiation. However, the effects of activation of NOD1 and NOD2, the two prominent members of NLR, on adipocyte differentiation have not been studied.
Design and Methods:
3T3-L1 and human adipose-derived stem cells were tested for adipocyte differentiation in the presence or absence of NOD ligand. Adipocyte differentiation was evaluated by the adipocyte markers gene expression and Oil Red O staining for lipid accumulation.
Activation of NOD1, but not NOD2, by a synthetic ligand dose-dependently suppressed 3T3-L1 adipocyte differentiation as revealed by Oil Red O stained cell morphology, lipid accumulation, and attenuated gene expression of adipocyte markers (PPARγ, C/EBPα, SCD, FABP4, Adiponectin). Activation of NOD1, but not NOD2, induced NF-κB activation, which correlated with their abilities to suppress ligand-induced PPARγ transaction. Moreover, the suppressive effect by NOD1 activation was reversed by IκB super-repressor which blocks NF-κB activation. The suppression by NOD1 ligand C12-iEDAP on adipocyte differentiation was reversed by small RNA interference targeting NOD1, demonstrating the specificity of NOD1 activation. In contrast, activation of NOD1 and NOD2 both significantly suppressed adipocyte differentiation of human adipose-derived adult stem cells, demonstrating the species specific effects of NOD activation. In contrast to enhanced leptin mRNA by LPS and TNFα, NOD1 activation suppressed leptin mRNA in adipocytes, suggesting the differential effects of NOD1 activation in adipocytes.
Overall, our results suggest that NOD1 represents a novel target for adipose inflammation in obesity.