Hentschel Hartmut, Nearing Jacqueline, Harris H William, Betka Marlies, Baum Michelle, Hebert Steven C, Elger Marlies
Max Planck Institute for Molecular Physiology, Dortmund, Germany.
Am J Physiol Renal Physiol. 2003 Sep;285(3):F430-9. doi: 10.1152/ajprenal.00081.2002. Epub 2003 May 20.
We recently cloned a homologue of the bovine parathyroid calcium receptor from the kidney of a spiny dogfish (Squalus acanthias) and termed this new protein SKCaR. SKCaR senses alterations in extracellular Mg2+ after its expression in human embryonic kidney cells (Nearing J, Betka M, Quinn S, Hentschel H, Elger M, Baum M, Bai M, Chattopadyhay N, Brown E, Hebert S, and Harris HW. Proc Natl Acad. Sci USA 99: 9231-9236, 2002). In this report, we used light and electron microscopic immunocytochemical techniques to study the distribution of SKCaR in dogfish kidney. SKCaR antiserum bound to the apical membranes of shark kidney epithelial cells in the following tubular segments: proximal tubules (PIa and PIIb), late distal tubule, and collecting tubule/collecting duct as well as diffusely labeled cells of early distal tubule. The highly specific distribution of SKCaR in mesial tissue as well as lateral countercurrent bundles of dogfish kidney is compatible with a role for SKCaR to sense local tubular Mg2+ concentrations. This highly specific distribution of SKCaR protein in dogfish kidney could possibly work in concert with the powerful Mg2+ secretory system present in the PIIa segment of elasmobranch fish kidney to affect recycling of Mg2+ from putative Mg2+-sensing/Mg2+-reabsorbing segments. These data provide support for the possible existence of Mg2+ cycling in elasmobranch kidney in a manner analogous to that described for mammals.
我们最近从棘鲨(Squalus acanthias)的肾脏中克隆出了牛甲状旁腺钙受体的一个同源物,并将这种新蛋白质命名为SKCaR。SKCaR在人胚肾细胞中表达后可感知细胞外Mg2+的变化(Nearing J,Betka M,Quinn S,Hentschel H,Elger M,Baum M,Bai M,Chattopadyhay N,Brown E,Hebert S,和Harris HW。美国国家科学院院刊99:9231 - 9236,2002)。在本报告中,我们使用光镜和电镜免疫细胞化学技术研究了SKCaR在棘鲨肾脏中的分布。SKCaR抗血清与鲨鱼肾脏上皮细胞的顶膜结合,这些细胞位于以下肾小管节段:近端小管(PIa和PIIb)、远曲小管晚期以及集合小管/集合管,还有远曲小管早期的弥漫性标记细胞。SKCaR在棘鲨肾脏的内侧组织以及外侧逆流束中的高度特异性分布,与SKCaR感知局部肾小管Mg2+浓度的作用相一致。SKCaR蛋白在棘鲨肾脏中的这种高度特异性分布可能与板鳃鱼类肾脏PIIa节段中强大的Mg2+分泌系统协同作用,以影响Mg2+从假定的Mg2+感知/ Mg2+重吸收节段的循环利用。这些数据为板鳃类肾脏中可能存在类似于哺乳动物所描述的Mg2+循环提供了支持。