Department of Medicine, Division of Nephrology, West China Hospital of Sichuan University, 37# Guoxue Road, Wuhou District, Chengdu, 610041 Sichuan, China.
Int Urol Nephrol. 2013 Apr;45(2):571-9. doi: 10.1007/s11255-012-0313-y. Epub 2012 Nov 8.
Impaired core I β3-Gal-T-specific molecular chaperone (Cosmc) expression-caused IgA1 aberrant O-glycosylation is one of the main pathogeneses of IgA nephropathy (IgAN).This study tried to elucidate whether mycophenolic acid (MPA) could up-regulate Cosmc expression of peripheral lymphocytes in IgAN patients and reverse the dys-O-glycosylation.
Peripheral lymphocytes of eighteen IgAN patients and twelve normal controls were isolated and cultured for 3-7 days with or without lipopolysaccharide (LPS) and MPA. Cosmc mRNA and protein expression levels were measured by real-time RT-PCR and western blot. IgA1 and O-glycosylation level were determined by enzyme-linked immunosorbent assay (ELISA) and VV lectin-binding test. Correlation analysis was performed between Cosmc expression levels and IgA1 O-glycosylation level.
Cosmc mRNA expression and IgA1 O-glycosylation level in IgAN patients were significantly lower than normal controls. Treatment of LPS could obviously inhibit the Cosmc expression and increase the IgA1 secretion in peripheral lymphocytes of IgAN patients, which resulted in a significantly increase in IgA1 aberrant glycosylation level. Addition of MPA could significantly increase the Cosmc expression level along with a decrease in IgA1 secretion, leading to a reverse of aberrant glycosylation. A significant positive correlation between the Cosmc expression and IgA1 O-glycosylation level was noticed.
MPA can up-regulate the Cosmc expression and reverse the IgA1 aberrant O-glycosylation level in peripheral lymphocytes of IgAN patients, which might be the underlying mechanism of mycophenolate mofetil (MMF) therapy used in treating IgAN.
核心 I β3-Gal-T 特异性分子伴侣(Cosmc)表达受损导致的 IgA1 异常 O-糖基化是 IgA 肾病(IgAN)的主要发病机制之一。本研究试图阐明霉酚酸(MPA)是否可以上调 IgAN 患者外周淋巴细胞的 Cosmc 表达并逆转异常的 O-糖基化。
分离并培养 18 例 IgAN 患者和 12 例正常对照者的外周淋巴细胞,分别在有无脂多糖(LPS)和 MPA 的条件下培养 3-7 天。通过实时 RT-PCR 和 Western blot 检测 Cosmc mRNA 和蛋白表达水平。通过酶联免疫吸附试验(ELISA)和 VV 凝集素结合试验测定 IgA1 和 O-糖基化水平。分析 Cosmc 表达水平与 IgA1 O-糖基化水平之间的相关性。
IgAN 患者外周淋巴细胞 Cosmc mRNA 表达和 IgA1 O-糖基化水平明显低于正常对照组。LPS 处理可明显抑制 IgAN 患者外周淋巴细胞 Cosmc 表达并增加 IgA1 分泌,导致 IgA1 异常糖基化水平显著增加。加入 MPA 可明显增加 Cosmc 表达水平,同时减少 IgA1 分泌,导致异常糖基化逆转。Cosmc 表达与 IgA1 O-糖基化水平之间存在显著正相关。
MPA 可上调 IgAN 患者外周淋巴细胞 Cosmc 表达并逆转 IgA1 异常 O-糖基化水平,这可能是霉酚酸酯(MMF)治疗 IgAN 的潜在机制。