Hirai Shizuka, Matsumoto Haruka, Moriya Naoko H, Kawachi Hiroyuki, Yano Hideo
Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa-oiwake, Sakyo-ku, Kyoto-shi 606-8502, Japan.
Domest Anim Endocrinol. 2007 Oct;33(3):269-80. doi: 10.1016/j.domaniend.2006.06.001. Epub 2006 Jun 23.
We investigated the effect of activin A and follistatin on the differentiation of bovine preadipocytes. Stromal-vascular (SV) cells containing preadipocytes were prepared from perirenal adipose tissue of approximately 30-month-old Japanese Black steers. After confluence, differentiation was induced by 1-methyl-3-isobutyl-xanthine, dexamethasone, insulin and troglitasone for 2 days, and then subsequently cultured for 6 days. The cells were treated with activin A during the induction of differentiation (the early phase of differentiation) or throughout the differentiation period. We measured the terminal differentiation markers such as glycerol-3-phosphate dehydrogenase (GPDH) activity, lipid accumulation, and the expression of adipocyte fatty acid-binding protein mRNA at the end of cultures. Activin A suppressed the induction of all differentiation markers regardless of the duration of treatment. The treatment with activin A also reduced the expression of peroxisome proliferator-activated receptor (PPAR) gamma and CCAAT/enhancer binding protein (C/EBP) alpha mRNAs without affecting the expression of C/EBPbeta mRNA. We also observed that follistatin completely rescued the inhibitory effect of activin A on bovine preadipocyte differentiation. Furthermore, the higher doses of follistatin increased GPDH activity even in the presence of activin A compared with the cells treated with neither activin A nor follistatin. Additionally, the SV cells expressed activin A and myostatin mRNAs. These results suggest that activin A inhibits bovine preadiopocyte differentiation via affecting transcriptional cascade upstream of PPARgamma and C/EBPalpha expressions, and that follistatin suppresses the inhibitory effect of activin A on bovine preadipocyte differentiation. Endogenous activin A and/or myostatin possibly inhibit the differentiation of bovine preadipocytes.
我们研究了激活素A和卵泡抑素对牛前体脂肪细胞分化的影响。从大约30月龄的日本黑牛的肾周脂肪组织中制备含有前体脂肪细胞的基质血管(SV)细胞。细胞汇合后,用1-甲基-3-异丁基黄嘌呤、地塞米松、胰岛素和曲格列酮诱导分化2天,然后继续培养6天。在分化诱导期(分化早期)或整个分化期用激活素A处理细胞。我们在培养结束时测量了终末分化标志物,如甘油-3-磷酸脱氢酶(GPDH)活性、脂质积累以及脂肪细胞脂肪酸结合蛋白mRNA的表达。无论处理持续时间如何,激活素A均抑制所有分化标志物的诱导。激活素A处理还降低了过氧化物酶体增殖物激活受体(PPAR)γ和CCAAT/增强子结合蛋白(C/EBP)α mRNA的表达,而不影响C/EBPβ mRNA的表达。我们还观察到卵泡抑素完全挽救了激活素A对牛前体脂肪细胞分化的抑制作用。此外,与未用激活素A和卵泡抑素处理的细胞相比,更高剂量的卵泡抑素即使在存在激活素A的情况下也能增加GPDH活性。另外,SV细胞表达激活素A和肌肉生长抑制素mRNA。这些结果表明,激活素A通过影响PPARγ和C/EBPα表达上游的转录级联反应来抑制牛前体脂肪细胞分化,并且卵泡抑素抑制激活素A对牛前体脂肪细胞分化的抑制作用。内源性激活素A和/或肌肉生长抑制素可能抑制牛前体脂肪细胞的分化。