Müller-Höcker J, Droste M, Kadenbach B, Pongratz D, Hübner G
Pathologisches Institut Universität München, West Germany.
Hum Pathol. 1989 Jul;20(7):666-72. doi: 10.1016/0046-8177(89)90154-8.
Lack of cytochrome-c oxidase activity and of cytochromes aa3 + b has been reported previously in the skeletal muscle of one of two siblings (Müller-Höcker et al, 1983). The present study reports a deficiency of immunoreactive enzyme protein in the skeletal muscle of both siblings, who had an identical fatal clinical course. In all specimens the defect did not involve the whole enzyme protein, but was selectively expressed in the mitochondrially derived subunits II/III and nuclear coded subunits VIIbc. Neither the specific fibers of the muscle spindles nor the mitochondria of the heart, liver, kidneys, vessel walls and/or gastrointestinal tract were affected. These results are most consistent with a primary nuclear defect being responsible for the organ specific and subunit selective expression of the enzyme defect.
先前已有报道称,在一对兄弟姐妹中的一人骨骼肌中缺乏细胞色素c氧化酶活性以及细胞色素aa3 + b(Müller-Höcker等人,1983年)。本研究报告了这对兄弟姐妹的骨骼肌中均存在免疫反应性酶蛋白缺乏的情况,他们有着相同的致命临床病程。在所有标本中,缺陷并不涉及整个酶蛋白,而是选择性地在线粒体衍生的亚基II/III和核编码的亚基VIIbc中表达。肌梭的特定纤维以及心脏、肝脏、肾脏、血管壁和/或胃肠道的线粒体均未受影响。这些结果最符合原发性核缺陷导致酶缺陷的器官特异性和亚基选择性表达这一情况。