Bachmeier M, Löffler G
Institute for Biochemistry, Genetics and Microbiology, University of Regensburg, Germany.
Eur J Biochem. 1997 Jan 15;243(1-2):128-33. doi: 10.1111/j.1432-1033.1997.0128a.x.
In the absence of serum and serum substitutes, insulin at high doses together with platelet-derived growth factor BB (PDGF BB), corticosterone, and 3-isobutyl-1-methyl-xanthine is required to stimulate differentiation of 3T3-L1 preadipocytes. Under these conditions the differentiating cells express the CCAAT/enhancer-binding proteins (C/EBP) C/EBPdelta, C/EBPbeta, and C/EBP alpha with a similar sequence as described for differentiating cells in the presence of serum. The major differences detected under serum-free conditions are as follows: (a) PDGF BB is the major stimulator of the expression of the C/EBPbeta isoform liver activator protein (LAP). (b) The expression of LAP is also increased in preconfluent, proliferating cells due to the treatment with PDGF BB. (c) A small protein of 20 kDa (p20C/EBPbeta is detected with the anti-C/EBPbeta antibody. It is synthesized at high levels in such cells, which subsequently express high levels of the differentiation markers C/EBP alpha and glycerol-3-phosphate dehydrogenase. (d) Treatment of cells with fibroblast growth factor-2 (bFGF) in addition to adipogenic hormones results in differentiation and C/EBP alpha expression only to a very moderate extent as compared to treatment with PDGF BB but leads to a strong expression of both C/EBPbeta and C/EBPdelta.
在没有血清和血清替代物的情况下,需要高剂量胰岛素与血小板衍生生长因子BB(PDGF BB)、皮质酮和3-异丁基-1-甲基黄嘌呤共同作用,以刺激3T3-L1前脂肪细胞分化。在这些条件下,分化细胞表达CCAAT/增强子结合蛋白(C/EBP)C/EBPδ、C/EBPβ和C/EBPα,其序列与在有血清存在时分化细胞中所描述的相似。在无血清条件下检测到的主要差异如下:(a)PDGF BB是C/EBPβ同工型肝激活蛋白(LAP)表达的主要刺激物。(b)由于用PDGF BB处理,在汇合前增殖细胞中LAP的表达也增加。(c)用抗C/EBPβ抗体检测到一种20 kDa的小蛋白(p20C/EBPβ)。它在这些细胞中高水平合成,随后这些细胞表达高水平的分化标志物C/EBPα和甘油-3-磷酸脱氢酶。(d)与用PDGF BB处理相比,除了脂肪生成激素外,用成纤维细胞生长因子-2(bFGF)处理细胞仅在非常适度的程度上导致分化和C/EBPα表达,但会导致C/EBPβ和C/EBPδ的强烈表达。