Bader D
J Cell Biol. 1981 Feb;88(2):338-45. doi: 10.1083/jcb.88.2.338.
Acetylcholine receptors (AChR) are organized in a discrete and predictable fashion in the postsynaptic regions of vertebrate skeletal muscle. When muscle is damaged, nerves and myofibers including muscular elements of the endplate degenerate, but the connective tissue elements survive. Muscle fibers regenerate within the basal lamina of the original myofiber. Postsynaptic differentiation in regenerated mammalian skeletal muscle can occur in different ways: (a) at the site of the original endplate in the presence or absence of the nerve, or (b) at ectopic regions of the regenerated myofiber in the presence of the nerve when the original endplate is not present. The present study used (125)I-alpha- bungarotoxin ((125)I-alpha-BuTX) and EM autoradiography to examine the density and distribution of AChR in postsynaptic structures regenerated at the site of the original endplate in the absence of the nerve and at ectopic sites of the myofiber in the presence of the nerve when the original endplate was removed. In regenerated myofibers, the density of alpha-BuTX-binding sites fell within the range of densities observed in uninjured muscle whether postsynaptic differentiation occurred at the site of the original endplate in the absence of the nerve or at an originally ectopic position of the regenerated myofiber. In addition, the distribution of alpha-BuTX-binding sites within the regenerated postsynaptic regions closely resembled the distribution of apha-BuTX- binding sites in uninjured muscle. Morphometric analysis was performed on postsynaptic structures formed at the site of the original endplate in the absence of the nerve or at an ectopic position of the regenerated myofiber by interaction of the nerve and muscle. Although variation in the depth of the primary cleft occurred, there was little difference between the overall structure of regenerated postsynaptic structures and that of endplates of uninjured muscles.
乙酰胆碱受体(AChR)以离散且可预测的方式排列在脊椎动物骨骼肌的突触后区域。当肌肉受损时,神经和肌纤维(包括终板的肌肉成分)会退化,但结缔组织成分会存活下来。肌纤维在原始肌纤维的基膜内再生。再生哺乳动物骨骼肌中的突触后分化可以通过不同方式发生:(a)在原始终板的部位,无论有无神经;或者(b)当原始终板不存在时,在有神经存在的情况下,在再生肌纤维的异位区域。本研究使用(125)I-α-银环蛇毒素((125)I-α-BuTX)和电子显微镜放射自显影术,来检查在无神经的情况下于原始终板部位再生的突触后结构中,以及在去除原始终板且有神经存在时于肌纤维异位部位再生的突触后结构中,AChR的密度和分布情况。在再生的肌纤维中,无论突触后分化是发生在无神经的原始终板部位,还是发生在再生肌纤维原本的异位位置,α-BuTX结合位点的密度都落在未受损肌肉中观察到的密度范围内。此外,再生突触后区域内α-BuTX结合位点的分布与未受损肌肉中α-BuTX结合位点的分布非常相似。通过神经与肌肉的相互作用,对在无神经的原始终板部位或再生肌纤维异位位置形成的突触后结构进行了形态计量分析。虽然初级裂隙的深度存在变化,但再生突触后结构的整体结构与未受损肌肉终板的整体结构之间几乎没有差异。