Yang Tianxin, Gao Zhong-Xiuzi, Mao Zi-Hui, Wu Peng
Department of Internal Medicine, University of Utah, Salt Lake City, Utah, United States.
Veterans Affairs Medical Center, Salt Lake City, Utah, United States.
Am J Physiol Renal Physiol. 2025 Feb 1;328(2):F239-F247. doi: 10.1152/ajprenal.00156.2024. Epub 2024 Nov 7.
Epithelial sodium channel (ENaC) represents a major route of Na reabsorption in the aldosterone-sensitive distal nephron where the bulk of ENaC activity is considered to occur in the cortical collecting duct (CCD). Relatively, ENaC activity in the medulla, especially the inner medulla, is often neglected. (Pro)renin receptor (PRR), also termed ATP6ap2, a newly characterized member of the renin-angiotensin system, has emerged as an important regulator of ENaC in the distal nephron. The ENaC regulatory action of PRR is largely mediated by the 28 kDa soluble PRR (sPRR). Although all three subunits of ENaC are under the control of aldosterone, sPRR only mediates the upregulation of α-ENaC but not the other two subunits. Furthermore, sPRR-dependent regulation of α-ENaC only occurs in the renal inner medulla but not in the cortex. sPRR also rapidly upregulates ENaC activity via Nox4-derived HO. Overall, sPRR has emerged as an important regulator of renal medullary Na reabsorption in the context of overactivation of the renin-angiotensin-aldosterone system.
上皮钠通道(ENaC)是醛固酮敏感远端肾单位中钠重吸收的主要途径,其中大部分ENaC活性被认为发生在皮质集合管(CCD)。相对而言,髓质尤其是内髓质中的ENaC活性常常被忽视。(前)肾素受体(PRR),也称为ATP6ap2,是肾素 - 血管紧张素系统新发现的成员,已成为远端肾单位中ENaC的重要调节因子。PRR对ENaC的调节作用很大程度上由28 kDa可溶性PRR(sPRR)介导。虽然ENaC的所有三个亚基都受醛固酮控制,但sPRR仅介导α-ENaC的上调,而不介导其他两个亚基。此外,sPRR对α-ENaC的依赖性调节仅发生在肾内髓质而非皮质。sPRR还通过Nox4衍生的HO迅速上调ENaC活性。总体而言,在肾素 - 血管紧张素 - 醛固酮系统过度激活的情况下,sPRR已成为肾髓质钠重吸收的重要调节因子。