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Par-1 promotes a hepatic mode of apical protein trafficking in MDCK cells

机译:Par-1促进MDCK细胞中顶端蛋白运输的肝模式

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Simple (i.e., nonstratified) epithelial cells use two different routes to target their newly synthesized luminal plasma membrane proteins to the cell surface: a direct route from the Golgi complex, as in the kidney-derived MDCK cell line, or an indirect route that involves a intermediate stop at the ab-luminal (basolateral) membrane, as in hepatocytes. The mechanisms or proteins responsible for these different protein targeting strategies are not known. Here, we show that increased expression of EMK1, a mammalian ortholog of Caenorhabditis elegans Par-1, in MDCK cells promotes a switch from a direct to a transcytotic mode of apical protein delivery and other trafficking changes typical of hepatocytes. These results, together with our recent demonstration that PAR-1 promotes morphological features of hepatocytes in MDCK cells, indicate that Par-1 modulates the developmental decision to build a columnar versus a hepatic epithelial cell. To our knowledge, Par-1 is the first gene assigned to this task in epithelial morphogenesis.
机译:简单的(即非分层)上皮细胞使用两种不同的途径将其新合成的腔质膜蛋白靶向到细胞表面:从高尔基复合体的直接途径,如在肾脏衍生的MDCK细胞系中,或涉及如肝细胞一样,在腹腔(基底外侧)膜的中间停止。负责这些不同蛋白质靶向策略的机制或蛋白质尚不清楚。在这里,我们显示MDK细胞中的秀丽隐杆线虫Par-1的哺乳动物直系同源基因EMK1的表达增加,促进了根尖蛋白递送从直接模式转换为跨细胞模式以及其他肝细胞典型的运输变化。这些结果,加上我们最近的研究表明PAR-1促进MDCK细胞中肝细胞的形态学特征,表明Par-1调节了构建柱状和肝上皮细胞的发育决定。据我们所知,Par-1是在上皮形态发生中分配给该任务的第一个基因。

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