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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Characterization of isoform expression and subcellular distribution of MYPT1 in intestinal epithelial cells
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Characterization of isoform expression and subcellular distribution of MYPT1 in intestinal epithelial cells

机译:肠上皮细胞中MYPT1同工型表达和亚细胞分布的表征

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摘要

The regulation of intestinal epithelial permeability requires phosphorylation of myosin regulatory light chain (MLC). The phosphorylation status of MLC is regulated by myosin light chain phosphatase (MLCP) activities. The activity of the catalytic subunit of MLCP (PP1c delta) toward MLC depends on its regulatory subunit (MYPT1). In this study, we revealed the presence of two MYPT1 isoforms, full length and variant 2 in human intestinal (Caco-2) epithelial cells and isolated intestinal epithelial cells (IECs) from mice. In confluent Caco-2 cells, MYPT1 was distributed at cell-cell contacts and colocalized with F-actin. These results suggest that MYPT1 isoforms are expressed in intestinal epithelial cells and MYPT1 may be involved in the regulation of intestinal epithelial barrier function. (C) 2016 Elsevier B.V. All rights reserved.
机译:肠上皮通透性的调节需要肌球蛋白调节轻链(MLC)的磷酸化。 MLC的磷酸化状态受肌球蛋白轻链磷酸酶(MLCP)活性的调节。 MLCP的催化亚基(PP1c delta)对MLC的活性取决于其调节性亚基(MYPT1)。在这项研究中,我们揭示了人类肠道(Caco-2)上皮细胞和小鼠分离的肠道上皮细胞(IEC)中存在两种MYPT1亚型,全长和变异体2。在融合的Caco-2细胞中,MYPT1分布在细胞间接触处,并与F-肌动蛋白共定位。这些结果表明,MYPT1亚型在肠上皮细胞中表达,MYPT1可能参与了肠上皮屏障功能的调节。 (C)2016 Elsevier B.V.保留所有权利。

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