Bohrmann J, Bonafede A
Institut für Biologie I, Zoologie, Universität Freiburg, Germany.
Int J Dev Biol. 2000 Dec;44(8):883-90.
Ductins represent membrane channel proteins which are supposed to form both proton channels in V-ATPases and connexon channels in gap junctions. In order to localize and characterize these proteins in different tissues of Drosophila, we applied indirect immunofluorescence microscopy and immunoblots, using antisera prepared against Drosophila ductin and against Nephrops ductin. Previously, these antisera have been shown to recognize, in ovarian follicles and young embryos of Drosophila, the ductin monomer of 16 kDa and a putative dimer of 29 kDa. Moreover, both anti-ductin sera label antigens in plasma membranes and in the cytoplasm and block, when microinjected, cell-cell communication via gap junctions. In the present study, comparing several embryonic, larval and adult tissues, the anti-ductin sera were found to recognize antigens with various locations in cells of the midgut, the salivary gland, the nervous system, the muscles and the epidermis. For example, in midgut cells, antigens were labeled mainly in apical plasma membranes and in the apical part of the cytoplasm, while in salivary-gland cells, labeling was found throughout the plasma membranes and the cytoplasm. We conclude that putative gap junctions were revealed in the salivary gland, the nervous system and the epidermis, while plasma membrane-associated putative V-ATPases were detected in the midgut, the salivary gland and the muscles. Moreover, V-ATPases associated with cytoplasmic vesicles were found in almost every tissue. On immunoblots of homogenates from various tissues, the anti-ductin sera specifically labeled bands of 16, 21 and 29 kDa. When comparing these bands using peptide mapping with V8 protease, we found that they represent closely related proteins. Therefore, either different ductins or modifications of a single ductin appear to be present in different cellular regions, cell types and developmental stages of Drosophila.
导管蛋白代表膜通道蛋白,它们被认为既能在V-ATP酶中形成质子通道,又能在间隙连接中形成连接子通道。为了在果蝇的不同组织中定位和表征这些蛋白,我们应用了间接免疫荧光显微镜和免疫印迹技术,使用针对果蝇导管蛋白和螯龙虾导管蛋白制备的抗血清。此前,这些抗血清已被证明在果蝇的卵巢卵泡和幼胚中能识别16 kDa的导管蛋白单体和一个假定的29 kDa二聚体。此外,两种抗导管蛋白血清都能标记质膜和细胞质中的抗原,并且在显微注射时会阻断通过间隙连接的细胞间通讯。在本研究中,通过比较几个胚胎、幼虫和成虫组织,发现抗导管蛋白血清能识别中肠、唾液腺、神经系统、肌肉和表皮细胞中不同位置的抗原。例如,在中肠细胞中,抗原主要标记在顶端质膜和细胞质顶端部分,而在唾液腺细胞中,在整个质膜和细胞质中都能发现标记。我们得出结论,在唾液腺、神经系统和表皮中发现了假定的间隙连接,而在中肠、唾液腺和肌肉中检测到了与质膜相关的假定V-ATP酶。此外,在几乎每个组织中都发现了与细胞质囊泡相关的V-ATP酶。在来自各种组织的匀浆免疫印迹中,抗导管蛋白血清特异性标记了16、21和29 kDa的条带。当使用V8蛋白酶进行肽图谱分析比较这些条带时,我们发现它们代表密切相关的蛋白质。因此,在果蝇的不同细胞区域、细胞类型和发育阶段,可能存在不同的导管蛋白或单一导管蛋白的修饰形式。