Krasteva Gabriela, Pfeil Uwe, Drab Marek, Kummer Wolfgang, König Peter
Institut für Anatomie und Zellbiologie, University of Giessen Lung Center, Justus-Liebig-Universität Giessen, Germany.
Respir Res. 2006 Aug 11;7(1):108. doi: 10.1186/1465-9921-7-108.
Caveolae are involved in diverse cellular functions such as signal transduction, cholesterol homeostasis, endo- and transcytosis, and also may serve as entry sites for microorganisms. Hence, their occurrence in epithelium of the airways might be expected but, nonetheless, has not yet been examined.
Western blotting, real-time quantitative PCR analysis of abraded tracheal epithelium and laser-assisted microdissection combined with subsequent mRNA analysis were used to examine the expression of cav-1 and cav-2, two major caveolar coat proteins, in rat tracheal epithelium. Fluorescence immunohistochemistry was performed to locate caveolae and cav-1 and -2 in the airway epithelium of rats, mice and humans. Electron-microscopic analysis was used for the identification of caveolae. CLSM-FRET analysis determined the interaction of cav-1alpha and cav-2 in situ.
Western blotting and laser-assisted microdissection identified protein and transcripts, respectively, of cav-1 and cav-2 in airway epithelium. Real-time quantitative RT-PCR analysis of abraded tracheal epithelium revealed a higher expression of cav-2 than of cav-1. Immunoreactivities for cav-1 and for cav-2 were co-localized in the cell membrane of the basal cells and basolaterally in the ciliated epithelial cells of large airways of rat and human. However, no labeling for cav-1 or cav-2 was observed in the epithelial cells of small bronchi. Using conventional double-labeling indirect immunofluorescence combined with CLSM-FRET analysis, we detected an association of cav-1alpha and -2 in epithelial cells. The presence of caveolae was confirmed by electron microscopy. In contrast to human and rat, cav-1-immunoreactivity and caveolae were confined to basal cells in mice. Epithelial caveolae were absent in cav-1-deficient mice, implicating a requirement of this caveolar protein in epithelial caveolae formation.
These results show that caveolae and caveolins are integral membrane components in basal and ciliated epithelial cells, indicating a crucial role in these cell types. In addition to their physiological role, they may be involved in airway infection.
小窝参与多种细胞功能,如信号转导、胆固醇稳态、内吞和转胞吞作用,还可能作为微生物的进入位点。因此,它们在气道上皮中的存在可能是预期的,但尽管如此,尚未得到研究。
采用蛋白质免疫印迹法、对刮除的气管上皮进行实时定量PCR分析以及激光辅助显微切割并随后进行mRNA分析,以检测大鼠气管上皮中两种主要的小窝衣被蛋白cav-1和cav-2的表达。进行荧光免疫组织化学定位大鼠、小鼠和人类气道上皮中的小窝以及cav-1和cav-2。采用电子显微镜分析鉴定小窝。利用共聚焦激光扫描显微镜-荧光共振能量转移(CLSM-FRET)分析原位确定cav-1α和cav-2的相互作用。
蛋白质免疫印迹法和激光辅助显微切割分别在气道上皮中鉴定出cav-1和cav-2的蛋白质和转录本。对刮除的气管上皮进行实时定量逆转录PCR分析显示,cav-2的表达高于cav-1。cav-1和cav-2的免疫反应性在大鼠和人类大气道的基底细胞膜以及纤毛上皮细胞的基底外侧共定位。然而,在小支气管的上皮细胞中未观察到cav-1或cav-2的标记。使用传统的双标记间接免疫荧光结合CLSM-FRET分析,我们在上皮细胞中检测到cav-1α和cav-2的关联。通过电子显微镜证实了小窝的存在。与人类和大鼠不同,cav-1免疫反应性和小窝局限于小鼠的基底细胞。在cav-1缺陷小鼠中上皮小窝缺失。这表明这种小窝蛋白在上皮小窝形成中是必需的。
这些结果表明,小窝和小窝蛋白是基底细胞和纤毛上皮细胞中的完整膜成分,表明它们在这些细胞类型中起关键作用。除了其生理作用外,它们可能还参与气道感染。