Bortell R, Owen T A, Ignotz R, Stein G S, Stein J L
Department of Cell Biology, University of Massachusetts Medical Center, Worcester 01655.
J Cell Biochem. 1994 Feb;54(2):256-63. doi: 10.1002/jcb.240540214.
Pre-adipocyte 3T3-L1 cells, after an appropriate induction stimulus, proceed through a defined change in morphology as differentiation progresses. Transforming growth factor beta 1 (TGF beta 1) is able to block the morphological and biochemical changes which occur with differentiation of these cells if given within 36-40 h of induction [Ignotz and Massague (1985): Proc Natl Acad Sci USA 82:8530-8534]. To begin to elucidate the role of the extracellular matrix in adipogenesis, as well as the mechanism whereby TGF beta 1 inhibits differentiation, we examined the expression of two extracellular matrix genes, type I (alpha 1) procollagen and fibronectin, as well as endogenous TGF beta 1. Confluent cells were induced to differentiate by treatment with insulin, dexamethasone, and isobutylmethylxanthine in the presence or absence of TGF beta 1. Following 6 days of treatment, the cells in the differentiated group acquired the rounded shape of mature adipocytes; the cytosol of these cells also contained numerous lipid-filled vesicles, as demonstrated by oil red O staining. Cells treated with the differentiation compounds in the presence of TGF beta 1 maintained the fibroblast-like appearance of control cells and did not stain with oil red O. At the level of gene expression, both procollagen and fibronectin mRNAs were down-regulated during differentiation of 3T3-L1 cells. When cells from the control or differentiation groups were treated with TGF beta 1, there was a 2-5-fold induction of procollagen and fibronectin mRNAs throughout the 6-day time course.(ABSTRACT TRUNCATED AT 250 WORDS)
前脂肪细胞3T3-L1在受到适当的诱导刺激后,会随着分化进程经历明确的形态变化。如果在诱导后36 - 40小时内给予转化生长因子β1(TGFβ1),它能够阻断这些细胞分化过程中发生的形态和生化变化[伊格诺茨和马萨格(1985年):《美国国家科学院院刊》82:8530 - 8534]。为了开始阐明细胞外基质在脂肪生成中的作用以及TGFβ1抑制分化的机制,我们检测了两种细胞外基质基因,I型(α1)前胶原和纤连蛋白以及内源性TGFβ1的表达。在有或没有TGFβ1存在的情况下,用胰岛素、地塞米松和异丁基甲基黄嘌呤处理汇合细胞以诱导其分化。处理6天后,分化组的细胞呈现出成熟脂肪细胞的圆形;这些细胞的胞质溶胶中也含有大量充满脂质的小泡,油红O染色证实了这一点。在TGFβ1存在下用分化化合物处理的细胞保持了对照细胞的成纤维细胞样外观,并且油红O染色不着色。在基因表达水平上,3T3-L1细胞分化过程中前胶原和纤连蛋白的mRNA均下调。当对照或分化组的细胞用TGFβ1处理时,在整个6天的时间进程中,前胶原和纤连蛋白的mRNA诱导了2 - 5倍。(摘要截短于250字)