Huard J, Tremblay J P
Neurobiology Laboratory, Laval University, Enfant-Jésus Hospital, Que., Canada.
Neurosci Lett. 1992 Mar 16;137(1):105-8. doi: 10.1016/0304-3940(92)90309-u.
A monoclonal antibody that reacts with a mid rod fragment of dystrophin was used to localize this protein in the central nervous system (CNS). Due to a low abundance of dystrophin in the CNS, an immunoperoxidase reaction amplified with a biotin-avidin system was used. All Purkinje cells in normal mice were dystrophin positive while the mdx mouse cerebellum was completely devoid of reaction. Dystrophin staining was present in the soma and dendrites of Purkinje cells but not in their axons. This uniform dystrophin labelling in the normal mouse Purkinje cells indicates that this protein is not only localized in synaptic contact regions of the CNS.
一种与肌营养不良蛋白中杆状片段发生反应的单克隆抗体被用于在中枢神经系统(CNS)中定位该蛋白。由于中枢神经系统中肌营养不良蛋白的丰度较低,因此使用了生物素-抗生物素蛋白系统放大的免疫过氧化物酶反应。正常小鼠的所有浦肯野细胞均为肌营养不良蛋白阳性,而mdx小鼠的小脑则完全没有反应。肌营养不良蛋白染色存在于浦肯野细胞的胞体和树突中,但不存在于它们的轴突中。正常小鼠浦肯野细胞中这种均匀的肌营养不良蛋白标记表明该蛋白不仅定位于中枢神经系统的突触接触区域。