[MC3T3-E1培养过程中β -肌动蛋白基因表达的变化]。

Y Moriya, Y Shibata, Y Abiko, H Takiguchi
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引用次数: 0

摘要

多种形式的肌动蛋白(α, β和γ -肌动蛋白)已被发现在各种哺乳动物细胞系和组织中使用高分辨率,二维凝胶电泳。α -肌动蛋白仅存在于分化的肌肉细胞中,其合成在培养过程中被诱导,β -肌动蛋白和γ -肌动蛋白同型是微丝的主要成分,微丝的结构被认为与细胞形态发生、运动和有丝分裂有关。最近的研究表明,哺乳动物肌动蛋白mRNA水平在细胞形状变化和体外细胞分化过程中受到调节。另一方面,Kodama等人从新生小鼠颅骨中分离出克隆的MC3T3-E1细胞,经过多次连续传代,MC3T3-E1细胞仍保留了产生和矿化骨样基质物质的能力。因此克隆对研究成骨细胞分化及钙化机制具有重要意义。研究表明,骨细胞在激素处理后呈现星状形态,这些变化明显与微填充的重组改变有关,从而导致成骨细胞表型的增强。我们现在检测了培养时间对MC3T3-E1细胞β -actin基因表达的影响,发现β -actin基因的表达随着培养时间的增加而降低。这些对肌动蛋白基因表达的影响提示-肌动蛋白可能参与体内骨重塑。
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[Change of beta-actin gene expression during culture on osteoblast-like cell line, MC3T3-E1].

Multiple forms of actin (alpha, beta, and gamma-actin) have been found in a variety of mammalian cell lines and tissues by the use of high resolution, two-dimensional gel electrophoresis. alpha-Actin is found only in differentiated muscle cells, and its synthesis is induced during myogenesis in culture, beta- and gamma-actin isotypes are the principal components of microfilaments, structures believed to be involved in cellular morphogenesis, motility, and mitosis. Recent studies have shown that mammalian actin mRNA levels are modulated in response to changes in cell shape and during cell differentiation in vitro. On the other hand, Kodama et al. isolated clone MC3T3-E1 cells from newborn mouse calvaria, which have retained the ability to produce and mineralize a bone-like ground substance after many serial passages. Thus clone is useful for studying osteoblast differentiation as well as the mechanism of calcification. It is demonstrated that bone cells assume a stellate morphology after some hormone treatment and these changes were clearly associated with altered reorganization of the microfillaments which resulted in an enhanced osteoblast phenotype. We have now examined the effect of culture day on expression of beta-actin gene in MC3T3-E1 cells and found that expression of beta-actin gene reduced with culture days. These alternative on the expression of actin gene suggest that beta-actin may be involved in bone remodeling in vivo.

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