Frishberg Y, Meyers C M, Kelly C J
Division of Nephrology-Hypertension, University of California, San Diego, USA.
Kidney Int. 1996 Jul;50(1):45-53. doi: 10.1038/ki.1996.285.
In contrast to the well characterized suppressive effect of cyclosporine A (CsA) on IL-2 gene transcription in T cells, other immunosuppressive effects of CsA have received less attention. We have examined the effect of CsA on the expression of the beta 2 integrin, LFA-1, and its counter receptor, ICAM-1, on a renal Ag-specific murine T cell clone and Ag-expressing renal tubular epithelial cells. We have found that CsA has a concentration dependent effect on the expression of both ICAM-1 mRNA and gene product on renal tubular cells. At 0.1 microgram/ml, CsA exhibits a costimulatory effect, with TNF alpha, on ICAM-1 expression. CsA at 1 to 5 micrograms/ml exhibits concentration dependent inhibition of ICAM-1 cell surface expression by the tubular cells. Although CsA does not inhibit ICAM-1 on T cells, it does inhibit surface expression of LFA-1. The concentration dependent effects of CsA on ICAM-1 expression correlate well with ICAM-1 dependent T cell adhesion to TNF alpha stimulated tubular epithelial cells. TGF-beta 1 has similar effects on ICAM-1 and LFA-1 expression as high dose CsA, but the CsA effects are not mediated through induced TGF-beta 1 expression. Our studies support the conclusion that CsA may bidirectionally alter ICAM-1 dependent cellular adhesive interactions. The inhibition of cytokine stimulated ICAM-1 expression at higher CsA concentrations would contribute to the overall immunosuppressive effect of the drug.
与环孢素A(CsA)对T细胞中白细胞介素-2基因转录具有明确特征的抑制作用相反,CsA的其他免疫抑制作用受到的关注较少。我们研究了CsA对肾抗原特异性小鼠T细胞克隆以及表达抗原的肾小管上皮细胞上β2整合素LFA-1及其配体ICAM-1表达的影响。我们发现,CsA对肾小管细胞上ICAM-1 mRNA和基因产物的表达具有浓度依赖性作用。在0.1微克/毫升时,CsA与肿瘤坏死因子α(TNFα)共同对ICAM-1表达产生共刺激作用。1至5微克/毫升的CsA对肾小管细胞ICAM-1细胞表面表达呈现浓度依赖性抑制。虽然CsA不抑制T细胞上的ICAM-1,但它确实抑制LFA-1的表面表达。CsA对ICAM-1表达的浓度依赖性作用与ICAM-1依赖性T细胞与TNFα刺激的肾小管上皮细胞的黏附密切相关。转化生长因子β1(TGF-β1)对ICAM-1和LFA-1表达的作用与高剂量CsA相似,但CsA的作用不是通过诱导TGF-β1表达介导的。我们的研究支持以下结论:CsA可能双向改变ICAM-1依赖性细胞黏附相互作用。较高浓度的CsA对细胞因子刺激的ICAM-1表达的抑制作用将有助于该药物的整体免疫抑制效果。