Zulian Alessandra, Sileikytė Justina, Petronilli Valeria, Bova Sergio, Dabbeni-Sala Federica, Cargnelli Gabriella, Rennison David, Brimble Margaret A, Hopkins Brian, Bernardi Paolo, Ricchelli Fernanda
C.N.R. Institute of Neurosciences at the Department of Biomedical Sciences, University of Padova, Italy.
Biochim Biophys Acta. 2011 Dec;1807(12):1600-5. doi: 10.1016/j.bbabio.2011.08.007. Epub 2011 Aug 26.
We have investigated the mechanism of rat-selective induction of the mitochondrial permeability transition (PT) by norbormide (NRB). We show that the inducing effect of NRB on the PT (i) is inhibited by the selective ligands of the 18kDa outer membrane (OMM) translocator protein (TSPO, formerly peripheral benzodiazepine receptor) protoporphyrin IX, N,N-dihexyl-2-(4-fluorophenyl)indole-3-acetamide and 7-chloro-5-(4-chlorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one; and (ii) is lost in digitonin mitoplasts, which lack an intact OMM. In mitoplasts the PT can still be induced by the NRB cationic derivative OL14, which contrary to NRB is also effective in intact mitochondria from mouse and guinea pig. We conclude that selective NRB transport into rat mitochondria occurs via TSPO in the OMM, which allows its translocation to PT-regulating sites in the inner membrane. Thus, species-specificity of NRB toward the rat PT depends on subtle differences in the structure of TSPO or of TSPO-associated proteins affecting its substrate specificity.
我们研究了降冰片烯(NRB)对大鼠线粒体通透性转换(PT)的选择性诱导机制。我们发现,NRB对PT的诱导作用:(i)被18kDa外膜(OMM)转位蛋白(TSPO,原外周型苯二氮䓬受体)原卟啉IX、N,N-二己基-2-(4-氟苯基)吲哚-3-乙酰胺和7-氯-5-(4-氯苯基)-1,3-二氢-1-甲基-2H-1,4-苯并二氮杂䓬-2-酮的选择性配体所抑制;(ii)在缺乏完整OMM的洋地黄皂苷处理的线粒体中消失。在这些线粒体中,PT仍可被NRB阳离子衍生物OL14诱导,与NRB不同的是,OL14在来自小鼠和豚鼠的完整线粒体中也有效。我们得出结论,NRB选择性转运至大鼠线粒体是通过OMM中的TSPO进行的,这使其能够转运至内膜中调节PT的位点。因此,NRB对大鼠PT的物种特异性取决于TSPO或影响其底物特异性的TSPO相关蛋白结构的细微差异。