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Lgl通过抑制PAR-3-aPKC-PAR-6复合物来介导顶端结构域的解体,从而确定顶端膜极性。

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

作者信息

Yamanaka Tomoyuki, Horikoshi Yosuke, Izumi Natsuko, Suzuki Atsushi, Mizuno Keiko, Ohno Shigeo

机构信息

Department of Molecular Biology, Yokohama City University, Graduate School of Medical Science, 3-9 Fuku-ura, Kanazawa-ku, Yokohama 236-0004, Japan.

出版信息

J Cell Sci. 2006 May 15;119(Pt 10):2107-18. doi: 10.1242/jcs.02938. Epub 2006 Apr 25.

Abstract

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 PAR-3-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 PAR-3-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.

摘要

基底外侧肿瘤抑制蛋白Lgl对于上皮细胞极性和组织形态的调节至关重要。最近的研究表明,在上皮细胞中,Lgl与另一种极性调节蛋白机制——顶端PAR-3-aPKC-PAR-6复合体之间存在物理和功能上的相互作用。然而,Lgl介导的上皮细胞极性调节机制仍不清楚。通过RNA干扰方法,我们在此表明,在Ca2+耗竭诱导的去极化MDCK细胞中,内源性Lgl是顶端膜结构域解体所必需的。重要的是,这种Lgl功能是通过抑制顶端PAR-3-aPKC-PAR-6复合体的活性来介导的。在胶原凝胶中使用二维或三维培养细胞进行的分析表明,Lgl的这种抑制性调节对于胶原介导的顶端膜结构域的重新建立和管腔形成至关重要。这些结果表明,基底外侧Lgl在顶端膜结构域的解体中起关键作用,以诱导顶端膜极性的定向,这是通过抑制顶端PAR-3-aPKC-PAR-6复合体的活性来介导的。

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