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用Ca2+激活的中性蛋白酶解剖揭示的比目鱼肌Z线和诱导Z线类似物的特性。

Properties of soleus muscle Z-lines and induced Z-line analogs revealed by dissection with Ca2+-activated neutral protease.

作者信息

Yamaguchi M, Robson R M, Stromer M H, Cholvin N R, Izumimoto M

出版信息

Anat Rec. 1983 Aug;206(4):345-62. doi: 10.1002/ar.1092060402.

Abstract

Rat soleus muscle Z-lines and Z-line anomalies induced by neostigmine methyl sulfate (NMS) and cat soleus muscle Z-lines and Z-line anomalies induced by tenotomy were examined by electron microscopy before and after dissection of muscle fibers with Ca2+-activated neutral protease (CAF) to elucidate structural properties of Z-lines and related Z-line-type structures. In both normal and treated muscles, interdigitation of thin (6-7 nm) filaments, which were continuous with I-filaments (actin) from adjacent sarcomeres, was observed at the Z-line in longitudinal section. Both neostigmine methyl sulfate and tenotomy treatments induced muscle atrophy associated with Z-line degradation, streaming, and irregular distribution and accumulation of Z-line material and Z-rod formation. Tenotomized muscle also was characterized by the presence of N-line-like bands and I-Z-I brushes. CAF digestion removed the electron-dense covering material from Z-rods and revealed a backbone of actin filaments. The origin of Z-rods, their structural similarity to Z-lines in longitudinal and cross section, and their susceptibility to CAF indicate that Z-rods are directly related to native Z-lines and are probably lateral polymers of a basic Z-line unit. The regular square net alignment (22 nm) of I-filaments (actin) in cross sections of I-Z-I brushes which contain no N-lines suggests that the I-square net arrangement near the Z-line is determined by Z-filament-actin filament interaction rather than by the N-line or other factors. The results suggest that I-filaments (actin) penetrate the mammalian Z-line and are Z-line constituents and that the width of Z-lines and the length of Z-rods are determined by the amount of overlap of actin filaments. The perpendicular periodicity of Z-rods and the zigzag-oblique arrowheadlike appearance seen in longitudinal sections of Z-lines are attributed to alpha-actinin.

摘要

用电子显微镜检查了硫酸新斯的明(NMS)诱导的大鼠比目鱼肌Z线和Z线异常以及跟腱切断术诱导的猫比目鱼肌Z线和Z线异常,检查是在使用Ca2+激活的中性蛋白酶(CAF)解剖肌纤维前后进行的,以阐明Z线和相关Z线类型结构的结构特性。在正常和处理过的肌肉中,在纵切面上的Z线处均观察到细(6-7纳米)肌丝的相互交错,这些细肌丝与相邻肌节的I肌丝(肌动蛋白)相连。硫酸新斯的明和跟腱切断术处理均诱导了与Z线降解、流动、Z线物质的不规则分布和积累以及Z小体形成相关的肌肉萎缩。跟腱切断的肌肉还具有N线样带和I-Z-I刷的特征。CAF消化去除了Z小体上的电子致密覆盖物质,并揭示了肌动蛋白丝的主干。Z小体的起源、它们在纵切和横切面上与Z线的结构相似性以及它们对CAF的敏感性表明,Z小体与天然Z线直接相关,并且可能是基本Z线单位的侧向聚合物。不含N线的I-Z-I刷横切面上I肌丝(肌动蛋白)规则的方形网格排列(22纳米)表明,Z线附近的I方形网格排列是由Z细丝-肌动蛋白丝相互作用决定的,而不是由N线或其他因素决定的。结果表明,I肌丝(肌动蛋白)穿透哺乳动物的Z线并是Z线的组成部分,并且Z线的宽度和Z小体的长度由肌动蛋白丝的重叠量决定。Z小体的垂直周期性以及在Z线纵切面上看到的锯齿状-斜箭头状外观归因于α-辅肌动蛋白。

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