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首页> 外文期刊>Journal of cell biology >Atypical Protein Kinase C Is Involved in the Evolutionarily Conserved Par Protein Complex and Plays a Critical Role in Establishing Epithelia-Specific Junctional Structures
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Atypical Protein Kinase C Is Involved in the Evolutionarily Conserved Par Protein Complex and Plays a Critical Role in Establishing Epithelia-Specific Junctional Structures

机译:非典型蛋白激酶C参与进化上保守的Par蛋白复合物,并在建立上皮特异性连接结构中起关键作用

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摘要

We have previously shown that during early Caenorhabditis elegans embryogenesis PKC-3, a C. elegans atypical PKC (aPKC), plays critical roles in the establishment of cell polarity required for subsequent asymmetric cleavage by interacting with PAR-3 [Tabuse, Y., Y. Izumi, F. Piano, K.J. Kemphues, J. Miwa, and S. Ohno. 1998. Development (Camb.). 125:3607鈥?614]. Together with the fact that aPKC and a mammalian PAR-3 homologue, aPKC-specific interacting protein (ASIP), colocalize at the tight junctions of polarized epithelial cells (Izumi, Y., H. Hirose, Y. Tamai, S.-I. Hirai, Y. Nagashima, T. Fujimoto, Y. Tabuse, K.J. Kemphues, and S. Ohno. 1998. J. Cell Biol . 143:95鈥?06), this suggests a ubiquitous role for aPKC in establishing cell polarity in multicellular organisms. Here, we show that the overexpression of a dominant-negative mutant of aPKC (aPKCkn) in MDCK II cells causes mislocalization of ASIP/PAR-3. Immunocytochemical analyses, as well as measurements of paracellular diffusion of ions or nonionic solutes, demonstrate that the biogenesis of the tight junction structure itself is severely affected in aPKCkn-expressing cells. Furthermore, these cells show increased interdomain diffusion of fluorescent lipid and disruption of the polarized distribution of Na+,K+-ATPase, suggesting that epithelial cell surface polarity is severely impaired in these cells. On the other hand, we also found that aPKC associates not only with ASIP/PAR-3, but also with a mammalian homologue of C. elegans PAR-6 (mPAR-6), and thereby mediates the formation of an aPKC-ASIP/PAR-3鈥揚AR-6 ternary complex that localizes to the apical junctional region of MDCK cells. These results indicate that aPKC is involved in the evolutionarily conserved PAR protein complex, and plays critical roles in the development of the junctional structures and apico-basal polarization of mammalian epithelial cells.
机译:先前我们已经表明,在秀丽隐杆线虫胚胎发生PKC-3早期,秀丽隐杆线虫非典型PKC(aPKC)在通过与PAR-3相互作用进行随后的不对称裂解所需的细胞极性的建立中起着关键作用[Tabuse,Y., Y.Izumi,F.Piano,KJ Kemphues,J。Miwa和S.Ohno。 1998年。发展(Camb。)。 125:3607-614]。连同aPKC和哺乳动物PAR-3同源物,aPKC特异性相互作用蛋白(ASIP)共同定位在极化上皮细胞的紧密连接处(Izumi,Y.,H.Hirose,Y.Tamai,S.I Hirai,Y. Nagashima,T. Fujimoto,Y. Tabuse,KJ Kemphues,and S. Ohno。1998. J. Cell Biol。143:95-?06),这表明aPKC在建立细胞极性中的普遍作用。多细胞生物。在这里,我们显示在MDCK II细胞中aPKC(aPKCkn)的显性负突变体的过表达导致ASIP / PAR-3的错误定位。免疫细胞化学分析以及离子或非离子溶质的细胞旁扩散测量表明,紧密连接结构本身的生物发生在表达aPKCkn的细胞中受到严重影响。此外,这些细胞显示出增加的区域性荧光脂质扩散和Na +,K + -ATPase极化分布的破坏,表明这些细胞中的上皮细胞表面极性严重受损。另一方面,我们还发现aPKC不仅与ASIP / PAR-3相关,而且与秀丽隐杆线虫PAR-6(mPAR-6)的哺乳动物同源物相关,从而介导aPKC-ASIP / PAR-3'扬AR-6三元复合物,位于MDCK细胞的顶端连接区域。这些结果表明aPKC参与进化上保守的PAR蛋白复合物,并在哺乳动物上皮细胞的连接结构和apico-基底极化的发展中发挥关键作用。

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