Astrow S H, Sutton L A, Thompson W J
Center for Developmental Biology, University of Texas, Austin 78712.
J Neurosci. 1992 May;12(5):1602-15. doi: 10.1523/JNEUROSCI.12-05-01602.1992.
We have generated a monoclonal antibody, designated mAb 3G2, which reacts with a subsarcolemmal component of the neuromuscular junction in adult rats. mAb 3G2 immunoreactivity lies beneath and between the ACh receptor-rich synaptic gutters, around the sole plate nuclei, and at/near sarcomeric Z-disks in the vicinity of the synapse. Localization of mAb 3G2 immunoreactivity to neuromuscular junctions begins postnatally and gradually increases to adult levels. The establishment of this synaptic localization is neurally regulated, as neonatal denervation prevents its occurrence. In adults, denervation results in a loss of synaptic immunoreactivity that returns upon reinnervation. The antigen is also found at the myotendinous junction; its localization here is innervation independent. mAb 3G2 recognizes a 41 kDa protein on immunoblots of extracts of newborn muscle. Based on its distribution within muscle fibers, its developmental and neural regulation, and its molecular weight, the protein recognized by mAb 3G2 can be distinguished from other known postsynaptic proteins. Its neural dependence and developmental regulation suggest that it may participate in synaptic stabilization, perhaps as the intracellular component in a chain of proteins that serve to tether the nerve terminal to the perijunctional region of the muscle fiber.
我们制备了一种单克隆抗体,命名为mAb 3G2,它可与成年大鼠神经肌肉接头的肌膜下成分发生反应。mAb 3G2的免疫反应性位于富含乙酰胆碱受体的突触沟下方和之间、底板核周围以及突触附近的肌节Z盘处或其附近。mAb 3G2免疫反应性在神经肌肉接头处的定位始于出生后,并逐渐增加至成年水平。这种突触定位的建立受神经调节,因为新生动物去神经会阻止其发生。在成年动物中,去神经会导致突触免疫反应性丧失,而再支配后则会恢复。该抗原也存在于肌腱结合处;其在此处的定位与神经支配无关。mAb 3G2在新生肌肉提取物的免疫印迹上识别出一种41 kDa的蛋白质。基于其在肌纤维内的分布、发育和神经调节以及分子量,mAb 3G2识别的蛋白质可与其他已知的突触后蛋白质区分开来。其对神经的依赖性和发育调节表明,它可能参与突触稳定,也许作为一系列蛋白质中的细胞内成分,这些蛋白质用于将神经末梢拴系到肌纤维的接头周区域。