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脂质A诱导针对培养的同基因大鼠肾小管细胞的细胞毒性抗体。

Lipid A induction of cytotoxic antibody to cultured syngeneic rat kidney tubular cells.

作者信息

Hemstreet G P, Enoch P G, Fine P R, Wheat R

出版信息

Kidney Int. 1981 Feb;19(2):275-80. doi: 10.1038/ki.1981.17.

Abstract

Syngeneic Fischer rat kidneys repeatedly injected with lipid A induced a cytotoxic antibody to cultured syngeneic rat kidney tubular cells. To test for antibodies in the serum of immunized animals, we disaggregated syngeneic rat kidney tubular cells with collagenase and trypsin and established them in short-term culture. Cultured kidney tubule cells were then radiolabeled 24 hours later with chromium 51 and cultured for an additional 24 hours. Rabbit antirat kidney tubule cell antibody served as the positive control antisera in a complement-dependent antibody cytotoxicity assay. Serum samples from animals whose kidneys were innoculated with Re glycolipid were then tested for antibody cytotoxicity. Autoantibody to syngeneic cultured kidney tubule cells was presented in the serum from these animals (P less than 0.01) as well as in the serum of animals injected i.p. with Re glycolipid when compared with saline controls. The cytotoxic antibody could be removed by absorbing with syngeneic cultured kidney tubule cell membranes. These results suggest that the glycolipid from the mutant strain Re 595 of Salmonella minnesota stimulates a crossreactive antibody to cultured rat kidney tubular cells. The methodology used in these experiments provides an in vitro models for investigating the importance of the immune system in the pathogenesis of pyelonephritis.

摘要

将脂多糖反复注射到同基因的Fischer大鼠肾脏中,可诱导产生针对培养的同基因大鼠肾小管细胞的细胞毒性抗体。为检测免疫动物血清中的抗体,我们用胶原酶和胰蛋白酶将同基因大鼠肾小管细胞分散,并进行短期培养。培养24小时后,用51铬对培养的肾小管细胞进行放射性标记,再培养24小时。在补体依赖性抗体细胞毒性试验中,兔抗大鼠肾小管细胞抗体用作阳性对照抗血清。然后检测肾脏接种了Re糖脂的动物的血清样本的抗体细胞毒性。与生理盐水对照组相比,这些动物的血清以及经腹腔注射Re糖脂的动物的血清中均出现了针对同基因培养的肾小管细胞的自身抗体(P小于0.01)。细胞毒性抗体可通过与同基因培养的肾小管细胞膜吸附而去除。这些结果表明,来自明尼苏达沙门氏菌Re 595突变株的糖脂可刺激产生针对培养的大鼠肾小管细胞的交叉反应性抗体。这些实验中使用的方法为研究免疫系统在肾盂肾炎发病机制中的重要性提供了一个体外模型。

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