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运动神经元疾病中肌肉细胞的DNA片段化及凋亡相关蛋白

DNA-fragmentation and apoptosis-related proteins of muscle cells in motor neuron disorders.

作者信息

Tews D S, Goebel H H, Meinck H M

机构信息

Division of Neuropathology, Johannes-Gutenberg-University Medical Center, Mainz, Germany.

出版信息

Acta Neurol Scand. 1997 Dec;96(6):380-6. doi: 10.1111/j.1600-0404.1997.tb00302.x.

Abstract

Apoptosis has been described as one of the mechanisms of muscle fiber loss in infantile spinal muscular atrophy. In order to investigate if muscle fiber-apoptosis plays a role in other denervating disorders as well, we studied DNA-fragmentation, a hallmark of apoptosis, by the TUNEL-method and, moreover, the expression patterns of apoptosis-related proteins in 2 patients suffering from ALS and in 6 patients with polyneuropathy. We identified DNA-cleavage in muscle fibers of all these patients. Furthermore, we found strong expression of bax and ICE promoting apoptosis in muscle fibers. However, also strong expression of the anti-apoptotic factor bcl-2 was found. Our findings indicate that defective innervation may prompt muscle fibers to activate an intrinsic "suicide" programme which is promoted by the proapoptotic factors bax and ICE, which seems to induce formation of apoptotic bodies by cleavage of actin. Nevertheless, there are also anti-apoptotic strategies in muscle fibers manifested by expression of the bax-antagonist bcl-2 which is able to neutralize high bax levels.

摘要

细胞凋亡被认为是婴儿型脊髓性肌萎缩症中肌纤维丧失的机制之一。为了研究肌纤维凋亡是否也在其他去神经疾病中起作用,我们通过TUNEL法研究了DNA片段化(细胞凋亡的一个标志),此外,还研究了2例肌萎缩侧索硬化症患者和6例多发性神经病患者中凋亡相关蛋白的表达模式。我们在所有这些患者的肌纤维中都发现了DNA裂解。此外,我们发现促进肌纤维凋亡的bax和ICE有强烈表达。然而,也发现了抗凋亡因子bcl-2的强烈表达。我们的研究结果表明,神经支配缺陷可能促使肌纤维激活由促凋亡因子bax和ICE促进的内在“自杀”程序,这似乎通过肌动蛋白裂解诱导凋亡小体的形成。尽管如此,肌纤维中也存在由bax拮抗剂bcl-2的表达所体现的抗凋亡策略,bcl-2能够中和高水平的bax。

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