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人类重症肌无力胸腺肌样细胞:全新的免疫组织化学和细胞内电生理学研究

Human myasthenia gravis thymic myoid cells: de novo immunohistochemical and intracellular electrophysiological studies.

作者信息

Furuya A, Kobayashi T, Kameda N, Tsukagoshi H

机构信息

Department of Neurology, Tokyo Medical and Dental University, Japan.

出版信息

J Neurol Sci. 1991 Feb;101(2):208-20. doi: 10.1016/0022-510x(91)90048-c.

Abstract

Thymic myoid cells from myasthenia gravis (MG) patients and controls were successfully grown in explant cultures: we have compared them with skeletal muscle cells cultured from biopsies in morphological, immunohistochemical and electrophysiological studies. Some mononucleate cells in thymus cultures were myoglobin- or desmin-positive, but they were much rarer than the otherwise similar fusing myoblasts in muscle cultures. Frequencies of cultured myoglobin-positive cells showed no difference between MG and control and male or female, but were lower in samples of malignant thymoma, in younger cases and in those with less severe MG. Electrophysiologically the resting membrane potentials of cultured thymic multinucleate cells were significantly less than those of cultured skeletal muscle cells, and action potentials by electrical stimulation were rarely observed. In thymus cultures from only one case with malignant thymoma, desmin-positive myotubes had spontaneous irregular contractions followed by electrical firings. It is concluded that there are myoid cells in MG and control thymuses which have the potential to become skeletal muscle fibers morphologically and electrophysiologically, although their frequency and proliferation in culture are quite low.

摘要

重症肌无力(MG)患者和对照组的胸腺肌样细胞在组织块培养中成功生长:我们在形态学、免疫组织化学和电生理学研究中,将它们与活检培养的骨骼肌细胞进行了比较。胸腺培养物中的一些单核细胞肌红蛋白或结蛋白呈阳性,但比肌肉培养物中其他方面类似的融合成肌细胞要少见得多。培养的肌红蛋白阳性细胞的频率在MG组和对照组之间以及男性和女性之间没有差异,但在恶性胸腺瘤样本中、较年轻的病例以及MG症状较轻的病例中较低。在电生理学方面,培养的胸腺多核细胞的静息膜电位明显低于培养的骨骼肌细胞,通过电刺激很少观察到动作电位。在仅一例恶性胸腺瘤患者的胸腺培养物中,结蛋白阳性的肌管有自发的不规则收缩,随后是电发放。结论是,MG患者和对照组的胸腺中存在肌样细胞,它们在形态学和电生理学上有成为骨骼肌纤维的潜力,尽管它们在培养中的频率和增殖相当低。

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