Infection and Immunity Lab, West China Medical Center, Sichuan University, Chengdu, China.
Acta Biochim Biophys Sin (Shanghai). 2010 Jan;42(1):70-9. doi: 10.1093/abbs/gmp109.
Leptospirosis renal disease is one of the common clinical manifestations of leptospirosis, including acute renal failure and tubulointerstitial nephritis. Outer membrane protein A-like protein Loa22 is a lipoprotein from Leptospira interrogans and has been suggested to be a corresponding virulence factor. However, the role of Loa22 in leptospiral nephropathy is not yet understood. In the present study, we constructed a vector and artificially expressed Loa22 in Escherichia coli BL21(DE)pLysS cells. After extensive purification, along with a GST tag protein control, Loa22 protein was used to test the cytotoxicity in cultured rat proximal tubule cells (NRK52E) and examine its effects on the induction of inflammatory responses. Using morphological examination, 2,3-bis(2-methoxy-4- nitro-5-sulfophenyl)-5-[(phenylamino)carbonyl]-2H-tetrazoium hydrixide absorbance, lactate dehydrogenase assays and an analysis of apoptosis via flow cytometry, it was found that Loa22 protein mediates a direct cytotoxic effect on NRK52E cells in a dose-dependent manner. Using real-time PCR, western blotting and immunofluorescence, it was found that Loa22 protein upregulates the expression of toll-like receptor 2 (TLR2), induces nitric oxide synthase and promotes the production of nitric oxide (NO) and monocyte chemoattractant protein-1 (MCP-1) by NRK52E cells. Additionally, using a TLR2 blocking antibody, it was found that enhanced NO and MCP-1 production by NRK52E cells after Loa22 stimulation requires the activation of TLR2. Collectively, our data suggested that Loa22 is a critical virulence factor of L. interrogans and is involved in the leptospiral nephropathy through mediating direct cytotoxicity and enhancing inflammatory responses.
钩端螺旋体病肾脏疾病是钩端螺旋体病的常见临床表现之一,包括急性肾衰竭和肾小管间质性肾炎。外膜蛋白 A 样蛋白 Loa22 是来自问号钩端螺旋体的脂蛋白,被认为是相应的毒力因子。然而,Loa22 在钩端螺旋体肾病中的作用尚不清楚。在本研究中,我们构建了一个载体,并在大肠杆菌 BL21(DE)pLysS 细胞中人工表达了 Loa22。经过广泛的纯化,以及 GST 标签蛋白对照,Loa22 蛋白被用于测试在培养的大鼠近端肾小管细胞 (NRK52E) 中的细胞毒性,并研究其对诱导炎症反应的影响。通过形态学检查、2,3-双(2-甲氧基-4-硝基-5-磺苯基)-5-[(苯氨基)羰基]-2H-四唑水合吸光度、乳酸脱氢酶测定和流式细胞术分析细胞凋亡,发现 Loa22 蛋白以剂量依赖的方式介导对 NRK52E 细胞的直接细胞毒性作用。通过实时 PCR、western blot 和免疫荧光,发现 Loa22 蛋白上调 TLR2 的表达,诱导一氧化氮合酶,并促进 NRK52E 细胞产生一氧化氮 (NO) 和单核细胞趋化蛋白-1 (MCP-1)。此外,使用 TLR2 阻断抗体,发现 Loa22 刺激后 NRK52E 细胞增强的 NO 和 MCP-1 产生需要 TLR2 的激活。综上所述,我们的数据表明,Loa22 是问号钩端螺旋体的一个关键毒力因子,通过介导直接细胞毒性和增强炎症反应参与钩端螺旋体肾病。