Kishore B K, Wade J B, Schorr K, Inoue T, Mandon B, Knepper M A
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda 20892-0951, Maryland.
Am J Physiol. 1998 Jul;275(1):F131-42. doi: 10.1152/ajprenal.1998.275.1.F131.
The synaptotagmins are a family of integral membrane proteins proposed to function as regulators of both exocytosis and endocytosis. Here, we have used immunochemical techniques and RT-PCR to assess sites of renal expression of synaptotagmin VIII. A polyclonal antibody was raised to a synthetic peptide corresponding to the carboxy-terminal 21 amino acids of mouse synaptotagmin VIII. On immunoblots of membrane fractions from renal cortex and medulla (and in several other tissues), the antibody labeled a 52-kDa band (absent with preimmune IgG). Immunofluorescence localization was carried out in tissue sections from rat kidney. The synaptotagmin VIII antibody labeled early proximal tubules, thin ascending limbs, thick ascending limbs, connecting tubules, and collecting ducts. In collecting ducts, both type A and B intercalated cells exhibited basolateral labeling, whereas principal cells were labeled chiefly in the apical and subapical portion of the cells. Thick ascending limbs were labeled in both the basolateral and apical regions. RT-PCR experiments using total RNA extracted from cortex and medulla or microdissected inner medullary collecting ducts gave a single band of appropriate size. Sequencing of the PCR product confirmed that the amplified target is synaptotagmin VIII. We conclude that synaptotagmin VIII is broadly expressed among renal tubule epithelia, raising the possibility that it is involved in regulation of transport and/or cell remodeling at several sites in the nephron and collecting duct.
突触结合蛋白是一类整合膜蛋白,被认为在胞吐作用和胞吞作用中均发挥调节作用。在此,我们运用免疫化学技术和逆转录聚合酶链反应(RT-PCR)来评估突触结合蛋白VIII在肾脏中的表达部位。我们制备了一种针对与小鼠突触结合蛋白VIII羧基末端21个氨基酸对应的合成肽的多克隆抗体。在肾皮质和髓质(以及其他几种组织)膜组分的免疫印迹中,该抗体标记出一条52 kDa的条带(免疫前IgG不存在此条带)。在大鼠肾脏组织切片中进行了免疫荧光定位。突触结合蛋白VIII抗体标记了早期近端小管、细段升支、粗段升支、连接小管和集合管。在集合管中,A型和B型闰细胞均表现出基底外侧标记,而主细胞主要在细胞的顶端和顶端下部分被标记。粗段升支在基底外侧和顶端区域均被标记。使用从皮质和髓质或显微解剖的内髓集合管中提取的总RNA进行的RT-PCR实验产生了一条大小合适的单一条带。PCR产物的测序证实扩增的靶标是突触结合蛋白VIII。我们得出结论,突触结合蛋白VIII在肾小管上皮细胞中广泛表达,这增加了其参与肾单位和集合管多个部位的转运调节和/或细胞重塑的可能性。