Wang Cheng, Ye Zengchun, Peng Hui, Tang Hua, Liu Xun, Chen Zhujiang, Yu Xueqing, Lou Tanqi
Department of Nephrology, the Third First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, China.
Nephrology (Carlton). 2009 Apr;14(2):213-8. doi: 10.1111/j.1440-1797.2008.01025.x.
Abnormal immunoglobulin (Ig)A1 is considered to play a pivotal role in IgA nephropathy. We used mouse podocytes as the experimental model to investigate the effect of aggregated IgA1 (aIgA1) isolated from IgA nephropathy (IgAN) patients on nephrin expression in podocytes through direct and indirect pathways.
Jacalin affinity chromatography and Sephacryl S-200 molecular sieve chromatography were used to isolate IgA1 from blood of IgAN patients which was therefore became aIgA1. Podocytes were incubated with aIgA1 or special mesangial medium. Nephrin expression in podocytes was measured by real-time polymerase chain reaction and western blot analysis.
Aggregated IgA1 from IgAN patients and healthy controls reduced nephrin expression in podocytes at mRNA and protein levels when compared with podocytes incubated with control medium (RPMI-1640 with 0.5% foetal bovine serum) (P<0.05). While medium from mesangial cells incubated with aIgA1 from IgAN inhibited nephrin expression in podocytes at mRNA and protein levels when compared with podocytes incubated with medium from mesangial cells with aIgA1 from healthy controls (P<0.05).
Our findings implicate that aIgA1 from IgAN patients could inhibit nephrin expression through direct and indirect pathways, although these mechanisms remain to be clarified.
异常免疫球蛋白A1(IgA1)被认为在IgA肾病中起关键作用。我们以小鼠足细胞为实验模型,通过直接和间接途径研究从IgA肾病(IgAN)患者分离出的聚集性IgA1(aIgA1)对足细胞中nephrin表达的影响。
采用jacalin亲和层析和Sephacryl S - 200分子筛层析从IgAN患者血液中分离IgA1,使其成为aIgA1。将足细胞与aIgA1或特殊系膜细胞培养基孵育。通过实时聚合酶链反应和蛋白质印迹分析测定足细胞中nephrin的表达。
与用对照培养基(含0.5%胎牛血清的RPMI - 1640)孵育的足细胞相比,IgAN患者和健康对照者的聚集性IgA1在mRNA和蛋白质水平上降低了足细胞中nephrin的表达(P<0.05)。与用来自健康对照者的含aIgA1的系膜细胞培养基孵育的足细胞相比,用来自IgAN患者的含aIgA1的系膜细胞培养基孵育的系膜细胞培养基在mRNA和蛋白质水平上抑制了足细胞中nephrin的表达(P<0.05)。
我们的研究结果表明,IgAN患者的aIgA1可通过直接和间接途径抑制nephrin的表达,尽管这些机制仍有待阐明。