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培养的血管平滑肌细胞间连接蛋白43间隙连接的表达取决于细胞表型。

Expression of connexin43 gap junctions between cultured vascular smooth muscle cells is dependent upon phenotype.

作者信息

Rennick R E, Connat J L, Burnstock G, Rothery S, Severs N J, Green C R

机构信息

Department of Anatomy and Developmental Biology, University College London, England.

出版信息

Cell Tissue Res. 1993 Feb;271(2):323-32. doi: 10.1007/BF00318619.

Abstract

The smooth muscle cell is the predominant cell type of the arterial media. In the adult vascular system, smooth muscle cells are found primarily in the contractile phenotype, but following injury or during atherosclerotic plaque formation the secretory synthetic phenotype is expressed. Recently it has been shown that gap junction connexin43 messenger RNA levels are six times higher in cultured smooth muscle cells in the synthetic phenotype than in intact aorta. We have modulated rabbit aortic smooth muscle cells in culture between the synthetic phenotype and one resembling the contractile phenotype, and correlated gap junction expression with phenotype. A dual labelling technique with antibodies against smooth muscle myosin and a synthetic peptide constructed to match a portion of the connexin43 gap junction protein was used for these experiments. Gap junctions are numerous between synthetic phenotype cells but few are observed between contractile cells. Rat aortic smooth muscle cells were also cultured and the growth and structure of gap junctions followed in the synthetic phenotype by use of freeze-fracture electron microscopy and immunohistochemical techniques. Junctional plaques are similar in structure to those observed in cardiac muscle, their size and number increasing with time in culture. The increased numbers of gap junctions between synthetic phenotype smooth muscle cells may be important during vessel development, following injury, or in atherosclerotic plaque formation.

摘要

平滑肌细胞是动脉中膜的主要细胞类型。在成体血管系统中,平滑肌细胞主要呈收缩表型,但在损伤后或动脉粥样硬化斑块形成过程中会表达分泌性合成表型。最近研究表明,合成表型的培养平滑肌细胞中缝隙连接蛋白43信使核糖核酸水平比完整主动脉中的高出六倍。我们在培养的兔主动脉平滑肌细胞中调控其在合成表型和类似收缩表型之间转换,并将缝隙连接表达与表型相关联。这些实验采用了针对平滑肌肌球蛋白的抗体和为匹配连接蛋白43缝隙连接蛋白一部分而构建的合成肽的双重标记技术。合成表型细胞之间缝隙连接众多,但收缩细胞之间观察到的较少。还培养了大鼠主动脉平滑肌细胞,并通过冷冻断裂电子显微镜和免疫组织化学技术观察合成表型中缝隙连接的生长和结构。连接斑在结构上与心肌中观察到的相似,其大小和数量随培养时间增加。合成表型平滑肌细胞之间缝隙连接数量的增加在血管发育、损伤后或动脉粥样硬化斑块形成过程中可能很重要。

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