Inhibition of preadipocyte differentiation by myostatin treatment in 3T3-L1 cultures

HS Kim, L Liang, RG Dean, DB Hausman… - Biochemical and …, 2001 - Elsevier
HS Kim, L Liang, RG Dean, DB Hausman, DL Hartzell, CA Baile
Biochemical and biophysical research communications, 2001Elsevier
Myostatin, a new TGF-β family member, is known as a muscle growth inhibitor, but its role in
adipocyte development has not been studied. To test the role of Myostatin in 3T3-L1
preadipocyte differentiation, we treated cultured 3T3-L1 preadipocytes with Myostatin
dissolved in 0.1% trifluoroacetic acid (TFA) during differentiation after they had become
confluent. Myostatin treatment significantly decreased glycerol-3-phosphate dehydrogenase
(GPDH) activity and oil Red-O staining compared to controls that did not receive Myostatin …
Myostatin, a new TGF-β family member, is known as a muscle growth inhibitor, but its role in adipocyte development has not been studied. To test the role of Myostatin in 3T3-L1 preadipocyte differentiation, we treated cultured 3T3-L1 preadipocytes with Myostatin dissolved in 0.1% trifluoroacetic acid (TFA) during differentiation after they had become confluent. Myostatin treatment significantly decreased glycerol-3-phosphate dehydrogenase (GPDH) activity and oil Red-O staining compared to controls that did not receive Myostatin. Western blot analysis showed that the expression levels of CCAAT/enhancer binding protein α (C/EBP α) and peroxisome proliferator-activated receptor γ (PPAR γ) were significantly decreased by Myostatin treatment (P < 0.05). However, the expression of C/EBP β was not significantly changed by the treatment (P > 0.05). From RT-PCR result, the relative level of leptin mRNA in Myostatin-treated cells was not significantly different (P > 0.1) from the level in cells without Myostatin treatment. Our data show that Myostatin, a secreted protein from muscle, inhibits preadipocyte differentiation in 3T3-L1 cells, which is mediated, in part, by altered regulation of C/EBP α and PPAR γ.
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