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Rab3D和肌动蛋白揭示了肺泡II型上皮细胞中不同的板层体亚群。

Rab3D and actin reveal distinct lamellar body subpopulations in alveolar epithelial type II cells.

作者信息

van Weeren Laura, de Graaff Anko M, Jamieson James D, Batenburg Joseph J, Valentijn Jack A

机构信息

Department of Biochemistry and Cell Biology, Faculty of Veterinary Medicine, University of Utrecht, Yalelaan 2, 3584 CM Utrecht, The Netherlands.

出版信息

Am J Respir Cell Mol Biol. 2004 Mar;30(3):288-95. doi: 10.1165/rcmb.2003-0264OC. Epub 2003 Aug 21.

Abstract

Rab3D is a small GTP-binding protein associated with secretory vesicles in various exocrine and endocrine cells, where it has been implicated in regulated exocytosis. Data obtained previously in pancreas have suggested that rab3D is involved in the coating of secretory granules with filamentous actin. In the present study we employed Western blot analysis, immunofluorescence, and immunoelectron microscopy to examine the distribution of rab3D in rat lung. Rab3D immunoreactivity was detected in bronchiolar Clara cells and alveolar epithelial type II (AET-II) cells. In both cell types, rab3D displayed preferential localization to secretory vesicles that were identified using specific antibodies against Clara Cell Secretory Protein and p180 lamellar body protein, respectively. Interestingly, rab3D was associated with only 24% of the lamellar bodies in AET-II cells. Rab3D-positive lamellar bodies were typically in close proximity of the apical plasma membrane, where exocytosis occurs. Another subpopulation of lamellar bodies, constituting only 2%, was not only rab3D-positive but could also be labeled with the filamentous-actin probe phalloidin. A third subpopulation, constituting 9%, displayed actin coating without rab3D staining. We propose that these three lamellar body subpopulations represent consecutive intermediates along the regulated exocytotic pathway, implying that rab3D release and actin coating are intimately linked processes.

摘要

Rab3D是一种小GTP结合蛋白,与各种外分泌和内分泌细胞中的分泌囊泡相关,在这些细胞中它参与调节性胞吐作用。先前在胰腺中获得的数据表明,rab3D参与分泌颗粒被丝状肌动蛋白包被的过程。在本研究中,我们采用蛋白质免疫印迹分析、免疫荧光和免疫电子显微镜来检测rab3D在大鼠肺中的分布。在细支气管的克拉拉细胞和肺泡II型上皮(AET-II)细胞中检测到Rab3D免疫反应性。在这两种细胞类型中,rab3D分别优先定位于使用针对克拉拉细胞分泌蛋白和p180板层小体蛋白的特异性抗体鉴定出的分泌囊泡上。有趣的是,rab3D仅与AET-II细胞中24%的板层小体相关。Rab3D阳性的板层小体通常靠近顶端质膜,即发生胞吐作用的位置。板层小体的另一个亚群仅占2%,不仅rab3D阳性,还可以用丝状肌动蛋白探针鬼笔环肽标记。第三个亚群占9%,显示有肌动蛋白包被但无rab3D染色。我们提出,这三个板层小体亚群代表了沿着调节性胞吐途径的连续中间体,这意味着rab3D释放和肌动蛋白包被是紧密相连的过程。

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