Pérez-Vázquez Victoriano, Saavedra-Molina Alfredo, Uribe Salvador
Instituto de Fisiología Celular, UNAM, Mexico, DF, México.
J Bioenerg Biomembr. 2003 Jun;35(3):231-41. doi: 10.1023/a:1024659615022.
The yeast mitochondrial unspecific channel (YMUC) sensitivity to inorganic (Ca2+ or Mg2+) or organic (hexyl or octyl-guanidine) cations was measured. The rate of oxygen consumption in State 3 and State 4, the transmembrane potential (deltapsi), mitochondrial swelling, and the polyethylene-glycol mediated recontraction were used to follow opening of the YMUC. Addition of 0.4 mM PO4 did not close the YMUC, although it did enhance the sensitivity to Ca2+ (I50 decreased from 50 to 0.3 mM) and Mg2+ (I50 decreased from 5 to 0.83 mM Mg2+). The Ca2+ concentration needed to close the YMUC was higher than the concentrations usually observed in the cell. Nonetheless, Mg2+, Ca2+, and PO4 exhibited additive effects. These cations did not inhibit contraction of preswollen mitochondria, suggesting that the YMUC/cation interaction was labile. Octyl-guanidine (OG-I50 7.5 microM) was the only cation which inhibited mitochondrial recontraction, probably as a result of membrane binding stabilization through its hydrophobic tail. The PO4-dependent, Ca(2+)/Mg(2+)-mediated closure of the YMUC may be a means to control the proportion of oxidative energy producing ATP or being lost as heat.
测定了酵母线粒体非特异性通道(YMUC)对无机阳离子(Ca2+或Mg2+)或有机阳离子(己基或辛基胍)的敏感性。使用状态3和状态4下的氧气消耗速率、跨膜电位(Δψ)、线粒体肿胀以及聚乙二醇介导的再收缩来跟踪YMUC的开放情况。添加0.4 mM的PO4并没有关闭YMUC,尽管它确实增强了对Ca2+(I50从50 mM降至0.3 mM)和Mg2+(I50从5 mM降至0.83 mM Mg2+)的敏感性。关闭YMUC所需的Ca2+浓度高于细胞中通常观察到的浓度。尽管如此,Mg2+、Ca2+和PO4表现出累加效应。这些阳离子并没有抑制预肿胀线粒体的收缩,这表明YMUC/阳离子相互作用是不稳定的。辛基胍(OG-I50为7.5 μM)是唯一抑制线粒体再收缩的阳离子,这可能是由于其疏水尾部使膜结合稳定化的结果。PO4依赖的、Ca(2+)/Mg(2+)介导的YMUC关闭可能是一种控制产生ATP的氧化能量比例或作为热量损失的比例的手段。