1Nephrology Division, MGH Center for Systems Biology, Program in Membrane Biology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
Am J Physiol Renal Physiol. 2013 Mar 1;304(5):F553-64. doi: 10.1152/ajprenal.00438.2011. Epub 2012 Dec 12.
Vasopressin (VP) binds to the vasopressin type 2 receptor (V2R) to trigger physiological effects including body fluid homeostasis and blood pressure regulation. Signaling is terminated by receptor downregulation involving clathrin-mediated endocytosis and V2R degradation. We report here that both native and epitope-tagged V2R are internalized from the plasma membrane of LLC-PK1 kidney epithelial cells in the presence of another ligand, transferrin (Tf). The presence of iron-saturated Tf (holo-Tf; 4 h) reduced V2R binding sites at the cell surface by up to 33% while iron-free (apo-Tf) had no effect. However, no change in green fluorescent protein-tagged V2R distribution was observed in the presence of bovine serum albumin, atrial natriuretic peptide, or ANG II. Conversely, holo-Tf did not induce the internalization of another G protein-coupled receptor, the parathyroid hormone receptor. In contrast to the effect of VP, Tf did not increase intracellular cAMP or modify aquaporin-2 distribution in these cells, although addition of VP and Tf together augmented VP-induced V2R internalization. Tf receptor coimmunoprecipitated with V2R, suggesting that they interact closely, which may explain the additive effect of VP and Tf on V2R endocytosis. Furthermore, Tf-induced V2R internalization was abolished in cells expressing a dominant negative dynamin (K44A) mutant, indicating the involvement of clathrin-coated pits. We conclude that Tf can induce heterologous downregulation of the V2R and this might desensitize VP target cells without activating downstream V2R signaling events. It also provides new insights into urine-concentrating defects observed in rat models of hemochromatosis.
血管加压素(VP)与血管加压素 2 型受体(V2R)结合,引发包括体液稳态和血压调节在内的生理效应。信号转导通过网格蛋白介导的内吞作用和 V2R 降解来终止受体下调。我们在这里报告,在另一种配体转铁蛋白(Tf)存在的情况下,内源性和表位标记的 V2R 均从 LLC-PK1 肾上皮细胞的质膜内化。铁饱和的 Tf(全 Tf;4 h)使细胞表面的 V2R 结合位点减少了多达 33%,而无铁的 Tf(脱铁 Tf)则没有影响。然而,在牛血清白蛋白、心钠肽或 ANG II 存在的情况下,未观察到绿色荧光蛋白标记的 V2R 分布的变化。相反,全 Tf 不会诱导另一种 G 蛋白偶联受体甲状旁腺激素受体的内化。与 VP 的作用相反,Tf 不会增加这些细胞内的 cAMP 或改变水通道蛋白-2 的分布,尽管 VP 和 Tf 一起添加会增强 VP 诱导的 V2R 内化。Tf 受体与 V2R 共免疫沉淀,表明它们密切相互作用,这可能解释了 VP 和 Tf 对 V2R 内吞作用的加性效应。此外,在表达显性负性动力蛋白(K44A)突变体的细胞中,Tf 诱导的 V2R 内化被废除,表明涉及网格蛋白包被的凹陷。我们得出结论,Tf 可以诱导 V2R 的异源下调,这可能使 VP 靶细胞脱敏而不激活下游 V2R 信号事件。它还为血色素沉着症大鼠模型中观察到的尿液浓缩缺陷提供了新的见解。