Hirai Shizuka, Matsumoto Haruka, Hino Naoko, Kawachi Hiroyuki, Matsui Tohru, 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 Jan;32(1):1-14. doi: 10.1016/j.domaniend.2005.12.001. Epub 2005 Dec 21.
We investigated the effect of myostatin on the differentiation of bovine preadipocyte. Stromal-vascular cells containing preadipocytes were prepared from perirenal adipose tissue of approximately 30-month-old Japanese Black steers. After confluence, the 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 myostatin 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 activity, lipid accumulation, and the expression of adipocyte fatty acid-binding protein mRNA at the end of cultures. The treatment with myostatin throughout the differentiation period severely suppressed the induction of all differentiation markers. The treatment with myostatin in the early phase of differentiation also suppressed the induction of terminal differentiation markers but three-fold higher dose of myostatin was required for the suppression compared with its treatment throughout the differentiation period. Myostatin treatment reduced the expression of peroxisome proliferator-activated receptor (PPAR) gamma mRNA and interfered with the induction of CCAAT/enhancer binding protein (C/EBP) alpha mRNA. We also observed that follistatin stimulates preadipocyte differentiation in the presence of myostatin. These results suggest that myostatin inhibits bovine preadiopocyte differentiation through suppressing PPARgamma and C/EBPalpha mRNA expressions and that follistatin counteracts the suppressive effect of myostatin.
我们研究了肌肉生长抑制素对牛前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脂肪细胞的基质血管细胞。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,随后再培养6天。在分化诱导期(分化早期)或整个分化期用肌肉生长抑制素处理细胞。在培养结束时,我们测量了终末分化标志物,如甘油-3-磷酸脱氢酶活性、脂质积累和脂肪细胞脂肪酸结合蛋白mRNA的表达。在整个分化期用肌肉生长抑制素处理严重抑制了所有分化标志物的诱导。在分化早期用肌肉生长抑制素处理也抑制了终末分化标志物的诱导,但与在整个分化期处理相比,抑制所需的肌肉生长抑制素剂量高3倍。肌肉生长抑制素处理降低了过氧化物酶体增殖物激活受体(PPAR)γ mRNA的表达,并干扰了CCAAT/增强子结合蛋白(C/EBP)α mRNA的诱导。我们还观察到,在存在肌肉生长抑制素的情况下,卵泡抑素可刺激前脂肪细胞分化。这些结果表明,肌肉生长抑制素通过抑制PPARγ和C/EBPα mRNA的表达来抑制牛前脂肪细胞分化,而卵泡抑素可抵消肌肉生长抑制素的抑制作用。