Lütcke A, Jansson S, Parton R G, Chavrier P, Valencia A, Huber L A, Lehtonen E, Zerial M
European Molecular Biology Laboratory, Heidelberg, Germany.
J Cell Biol. 1993 May;121(3):553-64. doi: 10.1083/jcb.121.3.553.
The rab subfamily of small GTPases has been demonstrated to play an important role in the regulation of membrane traffic in eukaryotic cells. Compared with nonpolarized cells, epithelial cells have distinct apical and basolateral transport pathways which need to be separately regulated. This raises the question whether epithelial cells require specific rab proteins. However, all rab proteins identified so far were found to be equally expressed in polarized and nonpolarized cells. Here we report the identification of rab17, the first epithelial cell-specific small GTPase. Northern blot analysis on various mouse organs, revealed that the rab17 mRNA is present in kidney, liver, and intestine but not in organs lacking epithelial cells nor in fibroblasts. To determine whether rab17 is specific for epithelial cells we studied its expression in the developing kidney. We found that rab17 is absent from the mesenchymal precursors but is induced upon their differentiation into epithelial cells. In situ hybridization studies on the embryonic kidney and intestine revealed that rab17 is restricted to epithelial cells. By immunofluorescence and immunoelectron microscopy on kidney sections, rab17 was localized to the basolateral plasma membrane and to apical tubules. Rab proteins associated with two distinct compartments have been found to regulate transport between them. Therefore, our data suggest that rab17 might be involved in transcellular transport.
小GTP酶的rab亚家族已被证明在真核细胞的膜运输调节中起重要作用。与非极化细胞相比,上皮细胞具有独特的顶端和基底外侧运输途径,需要分别进行调节。这就提出了一个问题,即上皮细胞是否需要特定的rab蛋白。然而,迄今为止鉴定出的所有rab蛋白在极化和非极化细胞中均有同等表达。在此,我们报告rab17的鉴定,它是第一个上皮细胞特异性小GTP酶。对各种小鼠器官进行的Northern印迹分析表明,rab17 mRNA存在于肾脏、肝脏和肠道中,但不存在于缺乏上皮细胞的器官中,也不存在于成纤维细胞中。为了确定rab17是否对上皮细胞具有特异性,我们研究了它在发育中的肾脏中的表达。我们发现rab17在间充质前体细胞中不存在,但在它们分化为上皮细胞时被诱导表达。对胚胎肾脏和肠道进行的原位杂交研究表明,rab17仅限于上皮细胞。通过对肾脏切片进行免疫荧光和免疫电子显微镜观察,rab17定位于基底外侧质膜和顶端小管。已发现与两个不同区室相关的Rab蛋白调节它们之间的运输。因此,我们的数据表明rab17可能参与跨细胞运输。