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培养的同基因肾小球系膜细胞激活自身反应性T淋巴细胞。

Activation of autoreactive T-lymphocytes by cultured syngeneic glomerular mesangial cells.

作者信息

Radeke H H, Emmendörffer A, Uciechowski P, von der Ohe J, Schwinzer B, Resch K

机构信息

Institute of Molecular Pharmacology, Medical School, Hannover, Germany.

出版信息

Kidney Int. 1994 Mar;45(3):763-74. doi: 10.1038/ki.1994.101.

Abstract

The capacity of intrinsic, glomerular mesangial cells (MC) to cause an autoreactive response of syngeneic lymphocytes in vitro are presented. Initial experiments demonstrated the MHC class II dependent capacity of MC to present exogenous antigen to sensitized lymph node lymphocytes (LN) and to activate naive, allogeneic LN in the absence of a nominal antigen. However, the most striking finding of the present investigation was that mouse MC (C57BL/6 or DBA/2) augmented a significant activation of naive, syngeneic lymphocytes. The extent of the proliferative lymphocyte response was comparable to that observed after stimulation with allogeneic MC. Moreover, during syngeneic coculture substantial amounts of interferon bioactivity were generated. Equipotent concentrations of rm IFN-gamma were sufficient to induce class II MHC expression of mouse MC. In control experiments the macrophage cell line, IC-21 (C57BL/6), or freshly prepared DBA/2 mouse peritoneal macrophages did not elicit a syngeneic LN response. Using MC, which had not been pretreated, the MC-specific LN stimulation occurred after prolonged periods of coculture. The stimulation index (S.I.) was 9.77 after 144 hours compared with LN controls (S.I. = 1). However, a 48 hour pretreatment of MC with either rm IFN-gamma alone or in combination with rh TNF-alpha and/or the continuous presence of rm IL-1 alpha during coculture periods from 72 to 144 hours substantially enhanced the proliferative LN response. Analysis of non-adherent LN by flow cytometry (FACS) after 96 or 120 hours coculture with MC revealed an increased ratio of Thy1.2+ to B220+ cells with a predominant rise of L3T4+ T-helper cells compared to Lyt2+ cytotoxic T-cells. Furthermore, immune fluorescence microscopy showed that a fraction of Thy1.2+ lymphoblasts adhered to MC. FACS analysis of these adherent LN after detachment demonstrated that in comparison to cocultures with untreated MC, cocultures of LN with IFN-gamma/TNF-alpha pre-treated MC resulted in a 24.4% increase of Thy1.2+ cells, with 89% of these being L3T4+ T-helper lymphocytes. In conclusion, autoreactivity of preferentially T-helper cells to cocultured glomerular MC was shown, which may represent a useful model of T-lymphocyte dependent glomerulonephritis.

摘要

本文展示了内源性肾小球系膜细胞(MC)在体外引发同基因淋巴细胞自身反应性应答的能力。初步实验证明,MC具有依赖MHC II类分子的能力,可将外源性抗原呈递给致敏淋巴结淋巴细胞(LN),并在无特异性抗原的情况下激活未致敏的同种异体LN。然而,本研究最显著的发现是,小鼠MC(C57BL/6或DBA/2)可增强未致敏同基因淋巴细胞的显著激活。淋巴细胞增殖反应的程度与同种异体MC刺激后观察到的程度相当。此外,在同基因共培养过程中产生了大量的干扰素生物活性。等效力浓度的重组干扰素-γ足以诱导小鼠MC表达II类MHC。在对照实验中,巨噬细胞系IC-21(C57BL/6)或新鲜制备的DBA/2小鼠腹腔巨噬细胞未引发同基因LN反应。使用未经预处理的MC,在长时间共培养后才出现MC特异性LN刺激。与LN对照(刺激指数=1)相比,144小时后的刺激指数为9.77。然而,在共培养72至144小时期间,单独用重组干扰素-γ或与重组肿瘤坏死因子-α联合预处理MC,或持续存在重组白细胞介素-1α,可显著增强LN增殖反应。与MC共培养96或120小时后,通过流式细胞术(FACS)分析非贴壁LN发现,与Lyt2+细胞毒性T细胞相比,Thy1.2+与B220+细胞的比例增加,其中L3T4+辅助性T细胞显著增多。此外,免疫荧光显微镜显示,一部分Thy1.2+淋巴母细胞粘附于MC。对这些脱离后的贴壁LN进行FACS分析表明,与未经处理的MC共培养相比,LN与干扰素-γ/肿瘤坏死因子-α预处理的MC共培养导致Thy1.2+细胞增加24.4%,其中89%为L3T4+辅助性T淋巴细胞。总之,研究表明优先辅助性T细胞对共培养的肾小球MC具有自身反应性,这可能代表了一种T淋巴细胞依赖性肾小球肾炎的有用模型。

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