骨骼肌的圆柱形螺旋起源于纵肌浆网

Jingwen Xu, Fu‐Chen Liu, Wei Li, Yuying Zhao, Dandan Zhao, Yue-Bei Luo, Jian-Qiang Lu, Chuan-zhu Yan
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引用次数: 5

摘要

在骨骼肌纤维中,柱状螺旋(CSs)是罕见但明显的肌层下堆积。迄今为止,仅在16例各种神经肌肉疾病患者中报道了CSs。CSs的起源和组成尚不清楚,尽管CSs和管状聚集体(TAs)在形态上有一些相似之处。为了明确CSs的性质,我们对2名中国成年兄弟姐妹肌肉活检的CSs中的肌浆网(SR)和其他细胞膜内系统蛋白进行了表征。免疫组织化学研究显示,纵向SR中sarco/内质网Ca2+- atp酶1 (SERCA 1)的肌上皮下免疫反应性,但对末端池中的calsequestrin或连接SR中的1型红嘌呤受体(RYR1)没有免疫反应性。2例TAs患者的肌肉活检显示,不仅对SERCA1有免疫反应性,而且对其他SR蛋白,包括calsequestrin和RYR1也有免疫反应性。CSs对高尔基体标记物GM130、核膜emerin、desmin、自噬体标记物LC3、溶酶体膜标记物LAMP2、肌营养不良蛋白或肌球蛋白均无免疫反应性。我们的研究结果表明,CSs可能仅起源于纵向SR,而TAs则由连接和纵向SR组成。免疫化学染色抗calsequestrin和RYR1抗体有助于区分这两种病理改变。
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Cylindrical Spirals in Skeletal Muscles Originate From the Longitudinal Sarcoplasmic Reticulum
Cylindrical spirals (CSs) are rare but distinct subsarcolemmal accumulations in skeletal muscle fibers. To date, CSs have been reported in only 16 patients with a variety of neuromuscular conditions. The origin and composition of CSs are unknown, although there are some morphologic similarities between CSs and tubular aggregates (TAs). To clarify the nature of CSs, we characterized the sarcoplasmic reticulum (SR) and other intracellular membrane system proteins in CSs of muscle biopsies from 2 adult Chinese siblings. Immunohistochemical studies revealed subsarcolemmal immunoreactivity for sarco/endoplasmic reticulum Ca2+-ATPase 1 (SERCA 1) in the longitudinal SR, but no immunoreactivity for calsequestrin in the terminal cisternae or type 1 ryanodine receptor (RYR1) in the junctional SR. Muscles biopsied from 2 patients with TAs showed immunoreactivity not only for SERCA1 but also for other SR proteins, including calsequestrin and RYR1. CSs exhibited no immunoreactivity for the Golgi apparatus marker GM130, the nuclear membrane emerin, desmin, the autophagosome marker LC3, the lysosomal membrane marker LAMP2, dystrophin, or myosin. Our results suggest CSs may originate only from the longitudinal SR, whereas TAs are composed of both the junctional and longitudinal SR. Immunochemical staining with antibodies against calsequestrin and RYR1 help to distinguish these 2 pathological alterations.
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