Department of Medical Biochemistry, Biology and Physics, University of Bari, Bari, Italy.
Mitochondrion. 2011 Mar;11(2):334-41. doi: 10.1016/j.mito.2010.12.004. Epub 2010 Dec 13.
In the present work we have critically examined the use of the KCN-titration technique in the study of the control of the cellular respiration by cytochrome c oxidase (COX) in the presence of the mitochondrial membrane potential (Δψ(mito)) in HepG2 cells. We clearly show that the apparent high inhibition threshold of COX in the presence of maximal Δψ(mito) is due to the KCN-induced decrease of Δψ(mito) and not to a low control of COX on the mitochondrial respiration. The tight control exerted by COX on the Δψ(mito) provides further insights for understanding the pathogenetic mechanisms associated with mitochondrial defects in human neuromuscular degenerative disorders.
在本工作中,我们批判性地研究了 KCN 滴定技术在研究 HepG2 细胞中线粒体膜电位 (Δψ(mito)) 存在时细胞色素 c 氧化酶 (COX) 对细胞呼吸控制的应用。我们清楚地表明,在最大 Δψ(mito) 存在下 COX 的表观高抑制阈值是由于 KCN 诱导的 Δψ(mito) 下降引起的,而不是 COX 对线粒体呼吸的低控制。COX 对 Δψ(mito) 的紧密控制为理解与人类神经肌肉退行性疾病中线粒体缺陷相关的发病机制提供了进一步的见解。