...
首页> 外文期刊>Journal of Cell Science >Lgl mediates apical domain disassembly by suppressing the PAR-3-aPKC-PAR-6 complex to orient apical membrane polarity
【24h】

Lgl mediates apical domain disassembly by suppressing the PAR-3-aPKC-PAR-6 complex to orient apical membrane polarity

机译:Lgl通过抑制PAR-3-aPKC-PAR-6复合物定向顶膜极性来介导顶结构域拆卸

获取原文
获取原文并翻译 | 示例

摘要

The basolateral tumor suppressor protein Lgl is important for the regulation of epithelial cell polarity and tissue morphology. Recent studies have shown a physical and functional interaction of Lgl with another polarity-regulating protein machinery, the apical PAR3-aPKC-PAR-6 complex, in epithelial cells. However, the mechanism of Lgl-mediated regulation of epithelial cell polarity remains obscure. By an siRNA method, we here show that endogenous Lgl is required for the disassembly of apical membrane domains in depolarizing MDCK cells induced by Ca2+ depletion. Importantly, this Lgl function is mediated by the suppression of the apical PAR3-aPKC-PAR-6 complex activity. Analysis using 2D- or 3D-cultured cells in collagen gel suggests the importance of this suppressive regulation of Lgl on the collagen-mediated re-establishment of apical membrane domains and lumen formation. These results indicate that basolateral Lgl plays a crucial role in the disassembly of apical membrane domains to induce the orientation of apical membrane polarity, which is mediated by the suppression of apical PAR-3-aPKC-PAR-6 complex activity.
机译:基底外侧肿瘤抑制蛋白Lgl对于调节上皮细胞极性和组织形态很重要。最近的研究表明,Lgl与上皮细胞中另一种极性调节蛋白机制,即顶端PAR3-aPKC-PAR-6复合物发生了物理和功能相互作用。然而,Lgl介导的上皮细胞极性调节机制仍然不清楚。通过siRNA方法,我们在这里显示内源性Lgl是由Ca2 +耗尽诱导的去极化MDCK细胞中的顶膜结构域拆卸所必需的。重要的是,该Lgl功能是通过抑制顶端的PAR3-aPKC-PAR-6复合物活性来介导的。在胶原蛋白凝胶中使用2D或3D培养的细胞进行的分析表明,Lgl的这种抑制性调节对胶原蛋白介导的顶膜结构域重建和管腔形成的重要性。这些结果表明,基底外侧Lgl在顶膜域的分解以诱导顶膜极性的取向中起关键作用,这是通过抑制顶体PAR-3-aPKC-PAR-6复合物活性来介导的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号