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Inhibition of 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) endocytosis by ouabain in human endothelial cells

机译:哇巴因对人内皮细胞内3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)内吞的抑制作用

摘要

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) uptake and reduction is widely used to evaluate cell proliferation and viability. MTT is taken up by the cells through endocytosis. We find that ouabain (1-200 nM) inhibits MTT reduction in human umbilical vein endothelial cells (HUVEC) without affecting cell viability. Ouabain does not inhibit MTT reduction when cell lysates substituted for the intact cells. Disruption of caveolae by cholesterol depletion, completely prevents the effect of ouabain. Treatment of HUVEC with Src inhibitor 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine partially abrogates the inhibitory effect of ouabain. The data suggest that ouabain interaction with caveolar Na/K-ATPase inhibits MTT endocytosis through the activation of signaling proteins such as Src kinase.
机译:3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)的摄取和还原被广泛用于评估细胞增殖和生存能力。细胞通过内吞作用吸收MTT。我们发现哇巴因(1-200 nM)抑制人脐静脉内皮细胞(HUVEC)的MTT降低,而不影响细胞活力。当细胞裂解液代替完整细胞时,瓦巴因不会抑制MTT的降低。胆固醇的消耗破坏小窝,完全阻止了哇巴因的作用。用Src抑制剂4-氨基-5-(4-氯苯基)-7-(叔丁基)吡唑并[3,4-d]嘧啶处理HUVEC,部分消除了哇巴因的抑制作用。数据表明哇巴因与小窝Na / K-ATPase的相互作用通过激活Src激酶等信号蛋白来抑制MTT的内吞作用。

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