Modulation of human T-lymphocyte plasma membrane Ca+2 permeability by imidazole antimycotics.

被引:7
作者
Hornstein, EH
Vassilopoulos, D
Thomas, DE
Friedman, FK
Tsokos, GC
机构
[1] WALTER REED ARMY MED CTR,DEPT MED,WASHINGTON,DC 20307
[2] NCI,MOLEC CARCINOGENESIS LAB,NIH,BETHESDA,MD 20892
[3] WALTER REED ARMY INST RES,DEPT CLIN PHYSIOL,WASHINGTON,DC 20307
关键词
D O I
10.3109/08923979609052734
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The role of cytochrome P-450 in the regulation of plasma membrane Ca+2 permeability of human peripheral T-lymphocytes by intracellular Ca+2 was examined. We assessed the effect of imidazole inhibitors of cytochrome P-450 on the intracytoplasmic free Ca+2 ([Ca+2]i) response generated using the microsomal ATPase inhibitor thapsigargin (THG) to deplete the intracellular Ca+2 stores. Econazole, miconazole and clotrimazole dramatically inhibited the THG mediated increase in [Ca-2]i and induced an increase in [Ca+2]i themselves. This inhibitory effect was previously observed in other cell systems and was attributed to inhibition of cytochrome P-450 by these agents. However, we evaluated a variety of structurally dissimilar P-450 inhibitors and found that none affected [Ca+2]i, indicating that the mechanism of imidazole action does not involve P-450.
引用
收藏
页码:237 / 245
页数:9
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