Effects of 3'-hydroxygenistein on proliferation and differentiation of 3T3-L1 preadipocytes and the underlying mechanisms
10.3724/SP.j.1008.2011.01181
- Author:
Li CHEN
1
Author Information
1. Department of Pharmacy
- Publication Type:Journal Article
- Keywords:
3'-hydroxygenistein;
Cell differentiation;
Cell proliferation;
PPAR gamma;
Preadipocyte
- From:
Academic Journal of Second Military Medical University
2011;32(11):1181-1185
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the effects of 3'-hydroxygenistein on the proliferation and differentiation of 3T3-L1 preadipocytes and to elucidate the related mechanism. Methods 3T3-L1 preadipocytes were cultured and treated with different dosages of 3'-hydroxygenistein. Cell proliferation was analyzed by counting cell numbers and MTT assay; DNA synthesis of 3T3-L1 was investigated by bromodeoxyuridine (BrdU) incorporation assay; the degree of preadipocytes differentiation was evaluated by Oil red O staffing; and the expressions of peroxisome proliferation activated receptor γ (PPARγ) and CAAT/ enhancer binding protein (C/EBPα) were detected at mRNA and protein level by real-time PCR and Western blolting analysis, respectively. Results Pretreatment with 3'-hydroxygenistrm (10-50 μmol/L) for 24, 48 and 72 h markedly promoted 3T3-L1 preadipocyte proliferation and differentiation in a dose-effect manner (P<0. 05, P<0. 01). It also significantly facilitated the DNA synthesis in 3T3-L1 preadipocytes in a dose-dependent manner (P< 0. 05). Similar to rosiglitazone (ROZ), 3'- hydroxygenistein (at 10 or 50 μmol/L) also resulted in more lipid droplets in 3T3-L1 preadipocytes (P<0. 05, P<0. 01). Furthermore, 3'-hydroxygenistein greatiy increased the mRNA and protein expression of PPARγ and C/EBPα in 3T3-L1 preadipocytes (P<0. 01). Conclusion 3'-hydroxygenistein can promote the proliferation and DNA synthesis of 3T3-L1 preadipocytes; it can also enhance the accumulation of lipid drops and increase the terminal differentiation of preadipocyts, which might be associated with its ablity to increase the expression of PPARγ and C/EBPα.
