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The adenomatous polyposis coli protein unambiguously localizes to microtubule plus ends and is involved in establishing parallel arrays of microtubule bundles in highly polarized epithelial cells

机译:腺瘤性息肉病大肠杆菌蛋白清楚地定位于微管的正末端并参与在高度极化的上皮细胞中建立微管束的平行阵列

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摘要

Loss of full-length adenomatous polyposis coli (APC) protein correlates with the development of colon cancers in familial and sporadic cases. In addition to its role in regulating β-catenin levels in the Wnt signaling pathway, the APC protein is implicated in regulating cytoskeletal organization. APC stabilizes microtubules in vivo and in vitro, and this may play a role in cell migration (Näthke, I.S., C.L. Adams, P. Polakis, J.H. Sellin, and W.J. Nelson. 1996. J. Cell Biol. 134:165–179; Mimori-Kiyosue, Y., N. Shiina, and S. Tsukita. 2000. J. Cell Biol. 148:505–517; Zumbrunn, J., K. Inoshita, A.A. Hyman, and I.S. Näthke. 2001. Curr. Biol. 11:44–49) and in the attachment of microtubules to kinetochores during mitosis (Fodde, R., J. Kuipers, C. Rosenberg, R. Smits, M. Kielman, C. Gaspar, J.H. van Es, C. Breukel, J. Wiegant, R.H. Giles, and H. Clevers. 2001. Nat. Cell Biol. 3:433–438; Kaplan, K.B., A. Burds, J.R. Swedlow, S.S. Bekir, P.K. Sorger, and I.S. Näthke. 2001. Nat. Cell Biol. 3:429–432). The localization of endogenous APC protein is complex: actin- and microtubule-dependent pools of APC have been identified in cultured cells (; ; Reinacher-Schick, A., and B.M. Gumbiner. 2001. J. Cell Biol. 152:491–502; Rosin-Arbesfeld, R., G. Ihrke, and M. Bienz. 2001. EMBO J. 20:5929–5939). However, the localization of APC in tissues has not been identified at high resolution. Here, we show that in fully polarized epithelial cells from the inner ear, endogenous APC protein associates with the plus ends of microtubules located at the basal plasma membrane. Consistent with a role for APC in supporting the cytoskeletal organization of epithelial cells in vivo, the number of microtubules is significantly reduced in apico-basal arrays of microtubule bundles isolated from mice heterozygous for APC.
机译:家族性和散发性病例中,全长腺瘤性息肉病大肠杆菌(APC)蛋白的丢失与结肠癌的发展有关。除了其在Wnt信号通路中调节β-catenin水平的作用外,APC蛋白还涉及调节细胞骨架的组织。 APC可在体内和体外稳定微管,这可能在细胞迁移中起作用(Näthke,IS,CL Adams,P。Polakis,JH Sellin和WJ Nelson。1996. J. Cell Biol。134:165-179; J。Cell Biol。 Mimori-Kiyosue,Y.,N。Shiina和S. Tsukita。2000. J. Cell Biol。148:505-517; Zumbrunn,J.,K. Inoshita,AA Hyman和ISNäthke。2001. Curr。Biol 。11:44–49)以及有丝分裂期间微管与动植物的连接(Fodde,R.,J. Kuipers,C. Rosenberg,R. Smits,M. Kielman,C. Gaspar,JH van Es,C. Breukel ,J。Wiegant,RH Giles和H.Clevers。2001. Nat。Cell Biol。3:433-438; Kaplan,KB,A。Burds,JR Swedlow,SS Bekir,PK Sorger和ISNäthke。2001。 (Cell Biol.3:429–432)。内源性APC蛋白的定位非常复杂:已在培养的细胞中鉴定了APC依赖肌动蛋白和微管的库(;; Reinacher-Schick,A.和BM Gumbiner。2001. J. Cell Biol。152:491-502 ; Rosin-Arbesfeld,R.,G. Ihrke和M. Bienz。2001. EMBO J. 20:5929-5939)。但是,尚未在高分辨率下确定APC在组织中的定位。在这里,我们显示,在来自内耳的完全极化的上皮细胞中,内源性APC蛋白与位于基质膜的微管的正端相关。与APC在体内支持上皮细胞的细胞骨架组织中的作用一致,从对APC杂合的小鼠中分离出的微管束的apico-基础阵列中的微管数量显着减少。

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