Leszczynski D
Transplantation Laboratory, University of Helsinki, Finland.
Am J Pathol. 1990 Jan;136(1):229-37.
Modulation of the major histocompatibility (MHC) antigen expression on rat endothelial cells by a mixture of cytokines has been examined. Experiments were performed employing both enzyme-linked immunoassay (ELISA) and fluorescence-activated cell-sorting (FACS) techniques and recombinant cytokines: interleukin-1 alpha (IL-1 alpha), tumor necrosis factor alpha (TNF alpha), and gamma-interferon (tau IFN). The results obtained show that TNF alpha enhances the effect of tau IFN on the expression of class I and II MHC antigens. IL-1 alpha did not affect tau IFN-induced class I expression but did inhibit tau IFN-induced class II expression. Finally, TNF alpha-induced class I MHC expression was inhibited strongly by IL-1 alpha. Pretreatment of endothelium with tau IFN did not potentiate the effects of IL-1 alpha or TNF alpha on the endothelial MHC antigen expression. These results suggest a possible anti-inflammatory role of IL-1 alpha via down-regulation of MHC antigen expression by the endothelium.
已研究了细胞因子混合物对大鼠内皮细胞主要组织相容性(MHC)抗原表达的调节作用。采用酶联免疫吸附测定(ELISA)和荧光激活细胞分选(FACS)技术以及重组细胞因子:白细胞介素-1α(IL-1α)、肿瘤坏死因子α(TNFα)和γ-干扰素(τ IFN)进行了实验。所得结果表明,TNFα增强了τ IFN对I类和II类MHC抗原表达的影响。IL-1α不影响τ IFN诱导的I类表达,但确实抑制了τ IFN诱导的II类表达。最后,IL-1α强烈抑制TNFα诱导的I类MHC表达。用τ IFN预处理内皮细胞并未增强IL-1α或TNFα对内皮MHC抗原表达的影响。这些结果表明IL-1α可能通过下调内皮细胞的MHC抗原表达发挥抗炎作用。