Coulson I H, Hurt G R, Holden C A
Skin Laboratory, St Helier Hospital, Carshalton, Surrey, U.K.
Br J Dermatol. 1991 Feb;124(2):124-9. doi: 10.1111/j.1365-2133.1991.tb00420.x.
Elevated activity of cyclic adenosine monophosphate-specific phosphodiesterase (PDE) has been previously documented in the peripheral blood mononuclear leucocytes (MNLs) of patients with atopic dermatitis (AD). Because of the potential interactions of the cyclic nucleotide and inositol secondary messenger systems we sought to determine whether differences exist in the inositol uptake and metabolism between atopic and normal MNLs. We found no difference in the uptake of tritiated inositol by MNL between 19 atopic patients and 16 non-atopic control subjects. However, after stimulation of MNLs by concanavalin A, there was a significantly greater metabolism of inositol to inositol-1-phosphate (IP1) in the controls compared to the atopic MNLs; the mean percentage rise in the IP1 fraction over baseline level was 40% in the atopics, but almost 200% in controls after 2 h. Diminished inositol metabolism in atopic MNLs may explain the reduced cell-mediated immunity that characterizes the atopic state.
先前有文献记载,特应性皮炎(AD)患者外周血单个核白细胞(MNLs)中环磷酸腺苷特异性磷酸二酯酶(PDE)的活性升高。由于环核苷酸和肌醇第二信使系统之间可能存在相互作用,我们试图确定特应性MNLs和正常MNLs在肌醇摄取和代谢方面是否存在差异。我们发现,19例特应性患者和16例非特应性对照受试者的MNLs对氚标记肌醇的摄取没有差异。然而,在用刀豆球蛋白A刺激MNLs后,与特应性MNLs相比,对照中肌醇代谢为肌醇-1-磷酸(IP1)的量显著增加;特应性患者中IP1部分相对于基线水平的平均升高百分比为40%,而对照在2小时后几乎为200%。特应性MNLs中肌醇代谢的减少可能解释了特应性状态所特有的细胞介导免疫降低的原因。