摘要
用细胞膜放射性标记和离子交换层析法、Ca ̄(2+)指示剂的分光光谱法和APAAP桥联酶标法分别检测M内IP_3、〔Ca ̄(2+)〕i和膜上Ia抗原的表达,研究IP_3受体阻断剂肝素(H)和钙调蛋白(CaRP)抑制剂三氟啦嗪(TFP)对NE调控MIa抗原表达的影响。结果显示:H(40μg/ml)不影响NE(10 ̄(-8)mol/L)增高M内IP_3的作用(452±30c.p.m./10 ̄6cells,NE组:442±22c.p.m./10 ̄6cells,P>0.05);但能阻断NE增高M〔Ca ̄(2+)〕i的作用(114±43nmol/L,NE组:322±76nmol/L,P<0.01);还能阻断NE促进MI-A、I-E表达的效应(46%±4%、45%±7%,NE组:64%±8%、58%±6%,P<0.01)。TFP(50μmol/L)不影响NE升高M〔Ca ̄(2+)〕的作用(328±89nmol/L,NE组:322±76nmol/L,P>0.05),却能阻断NE促进MI-A、I-E表达的效应(45%±4%、44%±5%,NE组:64%±8%、58%±6%,P<0.01)。结果提示:NE调控MIa抗原表达的效?
ell membrane isotope labelling and ion-exchange chromatography were used to determinethe IP_3 conten*t, Fura-2 was used as a fluorescence indicator to assav the intracellular calciumion concentration( Ca ̄(2+) i),and alkaline phosphatase anti-alkaline phosphatase(APAAP ) en-zyme immunoassay was used to detect the Ia antigen expression of rat peritoneal macrophages(MΦs). It was found that the effect of norepinephrine(NE,10 ̄(-8) nol/L,the same below) to in-crease Ca ̄(2+) i and to promote Ia antigen expression of the MΦs could be blocked by heparin(H,40μg/ml, the same below), an inositol triphosphate(IP_3) receptor blocking agent, despite thatthe latter did not interfere with the effect of NE to increase the IP_3 content of the MΦs.Triflu-operazine(TFP, 50μmol/L), an antagonist of the calcium regulatory protein (CaRP),could alsoblock the effect of NE to promote Ia antigen expression,without influencing the effect of NE toincrease Ca ̄(2+) i of the MΦs. These findings suggest that the promotive effect of NE of Ia anti-gen expression of the MΦs is dependent on the calcium ions released from calcium pool sensitiveto IP_3 stimulation and that binding of Ca ̄(2+) with CaRP is an indispensable step of the NE effectto promote Ia antigen expression on the MΦs.
出处
《中国免疫学杂志》
CSCD
北大核心
1994年第1期35-38,共4页
Chinese Journal of Immunology
基金
国家自然科学基金
关键词
巨噬细胞
去甲肾上腺素
抗原
肝素
Macrophage Norepinephrine Calcium ion concentration intra-cellular Ia antigen Heparin Trifluoperazine