Abstract. Sphingosine 1-phosphate (S1P) is a bioactive lipid mediator that regulates multiple signals through S1P receptors responsible for biological responses. In particular, the S1P 2 receptor has distinct roles in the S1P-mediated differentiation of certain cell types. The present study was the first, to the best of our knowledge, to report the role of the S1P 2 receptor in the adipocyte differentiation of 3T3-L1 pre-adipocytes. In order to investigate the influence of S1P 2 receptors in the anti-adipogenic effects of S1P, S1P 2 receptor silencing and overexpression of were used. S1P 2 overexpression with adenoviral vectors inhibited adipogenesis and inhibited the expression of peroxisome proliferator-activated receptor γ (PPARγ), adiponectin and CCAAT/enhancer binding protein-α, which were upregulated following incubation in differentiation media. Furthermore, S1P completely lost its ability to impair adipogenic differentiation following silencing of S1P 2 . Silencing of the S1P 2 receptor additionally blocked the downregulation of PPARγ protein and phospho-c-Jun N-terminal kinase protein induced by S1P treatment. In conclusion, the present study demonstrated that the S1P 2 receptor is a key signaling molecule in the S1P-dependent inhibition of adipogenic differentiation and additionally suggested that selective targeting of S1P 2 receptors may have clinical applications for the treatment of obesity.