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2'-'5-三腺苷酸对巨噬细胞腺苷酸环化酶和cAMP-磷酸二酯酶活性的影响
引用本文:尹桂山,王桂香,刘静芳,冯仁青,张书岑,陈寅,周月芳,刘新垣.2'-'5-三腺苷酸对巨噬细胞腺苷酸环化酶和cAMP-磷酸二酯酶活性的影响[J].中国生物化学与分子生物学报,1993,9(1):37-41.
作者姓名:尹桂山  王桂香  刘静芳  冯仁青  张书岑  陈寅  周月芳  刘新垣
作者单位:河北医学院生物化学教研室,河北医学院生物化学教研室,河北医学院生物化学教研室,河北医学院生物化学教研室,河北医学院生物化学教研室,中国科学院上海生物化学研究所,中国科学院上海生物化学研究所,中国科学院上海生物化学研究所 石家庄 050017,石家庄 050017,石家庄 050017,石家庄 050017,石家庄 050017,上海,上海,上海
摘    要:1989年,我们曾首次证实干扰素作用介导物pppA2'p5'A2'p5'A(2'-5'-三腺苷酸,2'-5'P_3A_3)能引起巨噬细胞中cAMP,cGMP水平升高,表明这两种环核苷酸在传递干扰素信息中起着重要作用。在上述研究的基础上,本研究观察了2'-5'P_3A_3对腺苷酸环化酶(AC)和cAMP-磷酸二酯酶(cAMP-PDE)两种酶的活性影响,结果发现,1×10~(-6)mol/L的2'-5'P_3A_3可显著增加AC的活性,而对cAMP-PDE活性沒有显著影响,这说明2'-5'P_3A_3引起的细胞内cAMP水平的升高是由于激活AC而使其生成增多,而不是抑制cAMP-PDE而使其降解减少的结果。

关 键 词:干扰素  2'-5'-三腺苷酸  腺苷酸环化酶  cAMP-磷酸二酯酶  
收稿时间:1993-02-20

Study on the Mechanism of Interferon Action: the Effect of 2'-5'P_3A_3 on the Activities of AC and cAMP-PDE in Macrophages
Yin,Gui-shan Wang,Cui-xang Liu,Jing-fang Feng,Ren-qing Zhang,Shu-ling.Study on the Mechanism of Interferon Action: the Effect of 2'-5'P_3A_3 on the Activities of AC and cAMP-PDE in Macrophages[J].Chinese Journal of Biochemistry and Molecular Biology,1993,9(1):37-41.
Authors:Yin  Gui-shan Wang  Cui-xang Liu  Jing-fang Feng  Ren-qing Zhang  Shu-ling
Institution:(Dept. of Biochem., Hebei Medical College, Shijiazhuang 050017) Chen,Yin Zhou,Yue-fang Liu, Xin-yuan (Shanghai Institute of Biochem., Academia Sinica, Shanghai
Abstract:In 1989, we first demonstrated that the mediator of interferon (IFN) action pppA2'p5'A2'p5'A (2'-5'-oligoadenylate, 2'-5'P_3A_3) may elevate the levels of the cellular cAMP and cGMP in macrophages, and suggested that both of the two nucleotides may play important roles in transmitting the messages of IFN. In this paper, the effect of 2'-5'P_3A_3 on the activities of AC and cAMP-PDE is examined on the basis of our preceeding research, we hare found that 1×10~(-6)mol/L of 2'-5' P_3A_3 may greatly increase the activity of AC, but has no effect on the activity of cAMP-PDE. It seems that the elevation of cellular cAMP level by 2'-5'P_3A_3 is due to the activition of AC, but not inhibiting of cAMP-PDE.
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