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巢蛋白在体内发育中的小鼠肢芽以及从肢芽分离的细胞微团培养物中的分布。

Distribution of nestin in the developing mouse limb bud in vivo and in micro-mass cultures of cells isolated from limb buds.

作者信息

Wroblewski J, Engström M, Edwall-Arvidsson C, Sjöberg G, Sejersen T, Lendahl U

机构信息

Department of Cell and Molecular Biology, Medical Nobel Institute, Karolinska Institutet, Stockholm, Sweden.

出版信息

Differentiation. 1997 Feb;61(3):151-9. doi: 10.1046/j.1432-0436.1997.6130151.x.

Abstract

Early skeletal muscle development is accompanied by changes in the composition of the cytoskeleton. In this report we analyze the distribution of the intermediate filament nestin in the developing mouse limb buds in vivo and in mesenchymal cells isolated from limb buds in vitro. The subcellular distribution of nestin mRNA and protein in muscle cells was also analyzed. We find a shift in nestin expression during early limb bud development. At embryonic day 11 (E11), low levels of nestin (protein) were expressed in the mesenchymal cells of the developing limb bud. Later, nestin mRNA and protein were down-regulated in the mesenchymal condensations undergoing chondrogenesis (E12 and E13), but remained expressed predominantly in the ectodermal cells and in the differentiating myoblasts. At E18, only muscle fibres, endothelial cells and nerves were nestin positive. This shift in expression was reproduced in vitro, in micro-mass cultures of mesenchymal cells. In E11 cultures, nestin protein was initially expressed in all cells. Upon formation of cartilage foci (after 2-3 days in culture), nestin immunoreactivity was not observed in cartilage, and low levels were detected in the cells located between the foci. A subpopulation of mono- and multinucleated cells, peripheral to the cartilage nodules, expressed the muscle-specific intermediate filament desmin protein together with high levels of nestin protein. The proportion of nestin-expressing cells could be changed by addition of specific signalling molecules. Insulin-like growth factors I and II (IGF I and II) increased the number of nestin-positive cells, while basic fibroblast growth factor (FGF) reduced the number of nestin-expressing cells. Finally, we present evidence for a different subcellular localization of nestin protein and mRNA: the mRNA is predominantly located in the ends of the muscle cell, whereas the protein is found in the central region. Intracellular localization of nestin mRNA may constitute an additional level of regulation of the cytoskeleton during muscle development.

摘要

早期骨骼肌发育伴随着细胞骨架组成的变化。在本报告中,我们分析了中间丝巢蛋白在体内发育中的小鼠肢芽以及体外从肢芽分离的间充质细胞中的分布情况。我们还分析了巢蛋白mRNA和蛋白在肌肉细胞中的亚细胞分布。我们发现在早期肢芽发育过程中巢蛋白表达发生了变化。在胚胎第11天(E11),发育中的肢芽间充质细胞中表达低水平的巢蛋白(蛋白)。之后,在经历软骨形成的间充质凝缩物中(E12和E13),巢蛋白mRNA和蛋白表达下调,但仍主要在外胚层细胞和分化的成肌细胞中表达。在E18时,只有肌纤维、内皮细胞和神经呈巢蛋白阳性。这种表达变化在体外间充质细胞的微团培养中也得到了重现。在E11培养物中,巢蛋白最初在所有细胞中表达。软骨灶形成后(培养2 - 3天后),在软骨中未观察到巢蛋白免疫反应性,而在灶之间的细胞中检测到低水平表达。软骨结节周围的单核和多核细胞亚群表达肌肉特异性中间丝结蛋白,同时巢蛋白表达水平较高。添加特定信号分子可改变巢蛋白表达细胞的比例。胰岛素样生长因子I和II(IGF I和II)增加了巢蛋白阳性细胞的数量,而碱性成纤维细胞生长因子(FGF)减少了巢蛋白表达细胞的数量。最后,我们提供了巢蛋白蛋白和mRNA不同亚细胞定位的证据:mRNA主要位于肌肉细胞的末端,而蛋白则位于中央区域。巢蛋白mRNA的细胞内定位可能构成肌肉发育过程中细胞骨架调控的一个额外层面。

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