Vandaele S F, Rieger F
Département de Pathologie, Université de Montréal, QC, Canada.
J Cell Sci. 1994 May;107 ( Pt 5):1217-27. doi: 10.1242/jcs.107.5.1217.
The surface distribution of the alpha 2/delta subunit of the 1,4-dihydropyridine receptor and its topographical relationship with the neural cell adhesion molecule (N-CAM) were investigated during early myogenesis in vitro, by double immunocytochemical labeling with the monoclonal antibody 3007 and an anti-N-CAM polyclonal antiserum. The monoclonal antibody 3007 has been previously shown to immunoprecipitate dihydropyridine receptor from skeletal muscle T-tubules. In further immunoprecipitation experiments on such preparations and muscle cell cultures, it was demonstrated here that the monoclonal antibody 3007 exclusively recognizes the alpha 2/delta subunit of the 1,4-dihydropyridine receptor. In rabbit muscle cell cultures, the labeling for both alpha 2/delta and N-CAM was first detected on myoblasts, in the form of spots on the membrane and perinuclear patches. Spots of various sizes organized in aggregates were then found on the membrane of myotubes. At fusion (T0), aggregates of N-CAM spots alone were found at the junction between fusing cells. At T6 and later stages, all alpha 2/delta aggregates present on myotubes co-localized with N-CAM, while less than 3% of N-CAM aggregates did not co-localize with alpha 2/delta. A uniform N-CAM staining also made its appearance. At T12, when myotubes showed prominent contractility, alpha 2/delta-N-CAM aggregates diminished in size. Dispersed alpha 2/delta spots of a small regular size spread over the whole surface of the myotubes and alignments of these spots became visible. Corresponding N-CAM spots were now occasionally seen, and uniform N-CAM staining was prominent. These results show that alpha 2/delta and N-CAM are co-localized and that their distributions undergo concomitant changes during early myogenesis until the T-tubule network starts to be organized. This suggest that these two proteins might jointly participate in morphogenetic events preceding the formation of T-tubules.
利用单克隆抗体3007和抗神经细胞黏附分子(N-CAM)多克隆抗血清进行双重免疫细胞化学标记,研究了体外早期肌发生过程中1,4-二氢吡啶受体α2/δ亚基的表面分布及其与神经细胞黏附分子的拓扑关系。单克隆抗体3007先前已被证明可从骨骼肌T小管中免疫沉淀二氢吡啶受体。在此对这些制剂和肌肉细胞培养物进行的进一步免疫沉淀实验中,证明单克隆抗体3007仅识别1,4-二氢吡啶受体的α2/δ亚基。在兔肌肉细胞培养物中,α2/δ和N-CAM的标记首先在成肌细胞上被检测到,呈膜上斑点和核周斑块的形式。然后在肌管膜上发现了大小各异的聚集成团的斑点。在融合时(T0),在融合细胞之间的连接处仅发现了N-CAM斑点聚集体。在T6及以后阶段,肌管上所有的α2/δ聚集体都与N-CAM共定位,而不到3%的N-CAM聚集体不与α2/δ共定位。均匀的N-CAM染色也出现了。在T12时,当肌管显示出明显的收缩性时,α2/δ-N-CAM聚集体的尺寸减小。小而规则的分散的α2/δ斑点分布在肌管的整个表面,并且这些斑点的排列变得可见。现在偶尔可以看到相应的N-CAM斑点,并且均匀的N-CAM染色很明显。这些结果表明,α2/δ和N-CAM是共定位的,并且它们的分布在早期肌发生过程中会伴随变化,直到T小管网络开始形成。这表明这两种蛋白质可能共同参与T小管形成之前的形态发生事件。