Renal Division, Department of Medicine, Peking University First Hospital, Beijing, China.
Peking University Institute of Nephrology, Beijing, China.
J Cell Mol Med. 2021 May;25(9):4316-4325. doi: 10.1111/jcmm.16492. Epub 2021 Mar 31.
Uromodulin (UMOD) can bind complement factor H (cFH) and inhibit the activation of complement alternative pathway (AP) by enhancing the cofactor activity of cFH on degeneration of C3b. UMOD, an N-glycans-rich glycoprotein, is expressed in thick ascending limb of Henle's loop where the epithelia need to adapt to gradient change of pH and ion concentration. ELISA-based cofactor activity of cFH and erythrocytes haemolytic assay was used to measure the impact of native and de-glycosylated UMOD on the functions of cFH. The binding assay was performed under different pH and ion concentrations, using ELISA. The levels of sialic acid on UMOD, from healthy controls and patients with chronic kidney disease (CKD), were also detected by lectin-ELISA. It was shown that removal of glycans decreased the binding between UMOD and cFH and abolished the ability of enhancing C3b degradation. In acidic condition, the binding became stronger, but it reduced as sodium concentration increased. A significant decrease of α-2,3 sialic acids on UMOD was observed in CKD patients compared with that of healthy individuals. The sialic acids on UMOD, local pH and sodium concentration could impact the binding capacity between UMOD and cFH and thus regulate the activation of complement AP.
尿调蛋白 (UMOD) 可以与补体因子 H (cFH) 结合,并通过增强 cFH 在 C3b 变性时的辅助因子活性来抑制补体替代途径 (AP) 的激活。UMOD 是一种富含 N-聚糖的糖蛋白,在 Henle 袢升支粗段表达,该处的上皮细胞需要适应 pH 值和离子浓度的梯度变化。基于 ELISA 的 cFH 辅助因子活性和红细胞溶血测定用于测量天然和去糖基化 UMOD 对 cFH 功能的影响。在不同的 pH 值和离子浓度下,通过 ELISA 进行结合测定。还通过凝集素-ELISA 检测来自健康对照者和慢性肾脏病 (CKD) 患者的 UMOD 上唾液酸的水平。结果表明,糖基去除降低了 UMOD 与 cFH 之间的结合,并消除了增强 C3b 降解的能力。在酸性条件下,结合变得更强,但随着钠离子浓度的增加而减少。与健康个体相比,CKD 患者的 UMOD 上的 α-2,3 唾液酸明显减少。UMOD 上的唾液酸、局部 pH 值和钠离子浓度可以影响 UMOD 和 cFH 之间的结合能力,从而调节补体 AP 的激活。