Tan An S, Berridge Michael V
Malaghan Institute of Medical Research, Wellington, New Zealand.
Redox Rep. 2004;9(6):302-6. doi: 10.1179/135100004225006777.
Trans-plasma membrane electron transport (tPMET) in mammalian cells has been demonstrated using artificial cell-impermeable dyes, but the extent to which reduction of these dyes involves distinct pathways remains unclear. Here we compare the properties of three commonly used dyes, WST-1, FeCN and DCIP. The presence of an intermediate electron carrier (mPMS or CoQ(1)) was obligatory for WST-1 reduction, whereas FeCN and DCIP were reduced directly. FeCN reduction was, however, greatly enhanced by CoQ(1), whereas DCIP was unaffected. Superoxide dismutase (SOD) and aminooxyacetate (AOA), a malate/aspartate shuttle inhibitor, strongly inhibited WST-1 reduction and reduced DCIP reduction by 40-60%, but failed to affect FeCN reduction, indicating involvement of mitochondrial TCA cycle-derived NADH and a possible role for superoxide in WST-1 but not FeCN reduction. Reduction of all three substrates was similarly inhibited by dicoumarol, diphenyleneiodonium and capsaicin. These results demonstrate that WST-1 FeCN and DCIP are reduced by distinct tPMET pathways.
利用人工合成的细胞不可渗透染料已证实哺乳动物细胞中存在跨质膜电子传递(tPMET),但这些染料的还原过程涉及不同途径的程度仍不清楚。在此,我们比较了三种常用染料WST-1、铁氰化物(FeCN)和2,6-二氯靛酚(DCIP)的特性。WST-1的还原需要中间电子载体(甲吩嗪硫酸甲酯或辅酶Q(1))的存在,而FeCN和DCIP可直接被还原。然而,辅酶Q(1)可极大增强FeCN的还原,而DCIP则不受影响。超氧化物歧化酶(SOD)和苹果酸/天冬氨酸穿梭抑制剂氨基氧乙酸(AOA)强烈抑制WST-1的还原,并使DCIP的还原降低40 - 60%,但对FeCN的还原无影响,这表明线粒体三羧酸循环衍生的NADH参与其中,并且超氧化物可能在WST-1而非FeCN的还原中发挥作用。双香豆素、二苯基碘鎓和辣椒素对所有三种底物的还原均有类似的抑制作用。这些结果表明,WST-1、FeCN和DCIP通过不同的tPMET途径被还原。