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静止的乳腺上皮细胞中连接蛋白43含量减少,但仍维持高水平的间隙连接细胞间通讯。

Quiescent mammary epithelial cells have reduced connexin43 but maintain a high level of gap junction intercellular communication.

作者信息

Sia M A, Woodward T L, Turner J D, Laird D W

机构信息

Department of Anatomy and Cell Biology, University of Western Ontario, London, Canada.

出版信息

Dev Genet. 1999;24(1-2):111-22. doi: 10.1002/(SICI)1520-6408(1999)24:1/2<111::AID-DVG11>3.0.CO;2-P.

Abstract

Gap junctions have been implicated in growth control, but it remains unclear whether cells that enter a quiescent state continue to express connexins and maintain a high level of gap junction intercellular communication (GJIC). To this end, MAC-T cells, a bovine mammary epithelial cell line, were serum starved for 48 h to induce a quiescent (G0) state. In quiescent cells, [3H]thymidine incorporation was reduced by 97.3% from serum-fed controls. Western blotting in conjunction with Phosphorlmager analysis revealed up to a 20-fold decrease in the expression of the gap junction protein connexin43 (Cx43 or alpha 1) and a shift toward the unphosphorylated form in quiescent cells. However, cell-to-cell transfer of the gap junction-permeable fluorescent tracer, Lucifer yellow, was only moderately reduced in quiescent cells. In control cells, Cx43 was predominantly perinuclear, although it was also present at sites of cell-cell apposition. In quiescent cells, intracellular labeling for Cx43 decreased without a corresponding reduction at areas of cell-cell contact. Recovery from serum deprivation resulted in increased thymidine incorporation that corresponded with an elevation in Cx43 protein expression and phosphorylation. In parallel studies, MAC-T cells were also induced to enter a quiescent state through contact inhibition. Despite a 20-fold reduction in 5-bromo-2'-deoxyuridine and a substantial reduction in intracellular Cx43, contact inhibited MAC-T cells also maintained gap junctions and GJIC. These experiments demonstrate that the maintenance of dye coupling in quiescent mammary cells is correlated with a redistribution of intracellular stores of Cx43.

摘要

缝隙连接与生长控制有关,但尚不清楚进入静止状态的细胞是否继续表达连接蛋白并维持高水平的缝隙连接细胞间通讯(GJIC)。为此,将牛乳腺上皮细胞系MAC-T细胞血清饥饿48小时以诱导静止(G0)状态。在静止细胞中,[3H]胸苷掺入量比血清喂养的对照降低了97.3%。蛋白质免疫印迹结合磷光成像分析显示,缝隙连接蛋白连接蛋白43(Cx43或α1)的表达在静止细胞中降低了20倍,并向未磷酸化形式转变。然而,缝隙连接可渗透的荧光示踪剂荧光黄在细胞间的转移在静止细胞中仅适度减少。在对照细胞中,Cx43主要位于核周,尽管它也存在于细胞-细胞接触部位。在静止细胞中,Cx43的细胞内标记减少,但细胞-细胞接触区域没有相应减少。从血清剥夺中恢复导致胸苷掺入增加,这与Cx43蛋白表达和磷酸化的升高相对应。在平行研究中,MAC-T细胞也通过接触抑制被诱导进入静止状态。尽管5-溴-2'-脱氧尿苷减少了20倍,细胞内Cx43大量减少,但接触抑制的MAC-T细胞也维持了缝隙连接和GJIC。这些实验表明,静止乳腺细胞中染料偶联的维持与Cx43细胞内储存的重新分布有关。

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