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肾成纤维细胞对来自活化淋巴细胞的生长抑制因子和基质减少因子敏感。

Renal fibroblasts are sensitive to growth-repressing and matrix-reducing factors from activated lymphocytes.

作者信息

Kitamura A, Kitamura M, Nagasawa R, Maruyama N, Mitarai T, Takahashi T, Isoda K

机构信息

Department of Internal Medicine, Saitama Medical Center, Japan.

出版信息

Clin Exp Immunol. 1993 Mar;91(3):516-20. doi: 10.1111/j.1365-2249.1993.tb05934.x.

Abstract

Various forms of nephropathy accompany interstitial fibrosis with lymphocytic infiltration. To probe the relationship between lymphocyte-derived factors and renal fibroblasts, we studied the effect of culture supernatant from lymphocytes stimulated by concanavalin A (ConASN) on the growth and matrix metabolism of rat kidney fibroblasts. 3H-thymidine incorporation and Northern analysis, respectively, revealed that ConASN repressed cell growth and the mRNA level of collagen type I, but dramatically elevated the steady-state expression of metalloproteinase transin/stromelysin. The growth inhibitor in ConASN was moderately heat-sensitive and less than 5 kD in molecular size, qualities that differed from those of transforming growth factor-beta (TGF-beta), IL-1 beta, IL-6, and tumour necrosis factor-alpha (TNF-alpha). The matrix regulatory factor in ConASN was highly heat-sensitive and more than 30 kD in size. Among several lymphokines tested, TNF-alpha produced the same effects as ConASN on the metabolism of extracellular matrix. We hypothesize that lymphocyte-derived factors have a significant role in the attenuation of renal fibrogenesis, as well as its progression, via inhibiting cell growth and matrix accumulation.

摘要

各种形式的肾病都伴有间质纤维化和淋巴细胞浸润。为了探究淋巴细胞衍生因子与肾成纤维细胞之间的关系,我们研究了伴刀豆球蛋白A刺激的淋巴细胞培养上清液(ConASN)对大鼠肾成纤维细胞生长和基质代谢的影响。3H-胸腺嘧啶核苷掺入法和Northern分析分别显示,ConASN抑制细胞生长和I型胶原的mRNA水平,但显著提高金属蛋白酶transin/基质溶解素的稳态表达。ConASN中的生长抑制剂对热有中度敏感性,分子大小小于5 kD,这些特性与转化生长因子-β(TGF-β)、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)不同。ConASN中的基质调节因子对热高度敏感,大小超过30 kD。在测试的几种淋巴因子中,TNF-α对细胞外基质代谢产生与ConASN相同的作用。我们推测,淋巴细胞衍生因子通过抑制细胞生长和基质积累,在肾纤维化形成的减弱及其进展中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81c5/1554705/c4784febc681/clinexpimmunol00041-0178-a.jpg

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