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体外血清诱导脱髓鞘的初始结构损伤。

The initial structural lesion in serum-induced demyelination in vitro.

作者信息

Bornstein M B, Raines C S

出版信息

Lab Invest. 1976 Oct;35(4):391-401.

PMID:979167
Abstract

Myelinated cultures of mouse spinal cord were exposed to sera obtained from rabbits affected by experimental allergic encephalomyelitis following challenge with whole white matter in complete Freund's adjuvant. In the presence of complement, the tissue response begins with an increased birefringence of its myelin sheaths. This is rapidly followed by a gamut of changes leading to demyelination. This study reports that, in the absence of complement, the response is arrested at the stage of increased birefringence. In this way, this early stage of the demyelinating process was available for detailed examination by light and electron microscopy. The brightened myelin sheaths appeared with a few hours of exposure and were seen around all axons and sometimes around cell bodies. This was often accompanied by abrupt breaks in the sheaths and angularly shaped myelin figures. Examination by electron microscope revealed a uniform increase in the myelin period from 11 nm. to 22 nm. The normally double intraperiod line was increased to four electron-dense leaflets, the additional two appearing to be derived from the close apposition of an additional electron-dense layer on the outer surface of the myelin sheath or oligodendrocytic membrane. Oligondendrocytes responsed with a prolific growth of processes whose membranes compacted to form swollen myelin. Neurons, astrocytes, and neuropil showed no changes. In its early stages, at least, the swelling was reversible. It would appear, therefore, that we have isolated the first stage of antiserum-induced demyelination in vitro, a stage which is now available for further study.

摘要

将小鼠脊髓的有髓培养物暴露于实验性变应性脑脊髓炎兔在完全弗氏佐剂中用全白质攻击后获得的血清。在补体存在的情况下,组织反应始于髓鞘双折射增加。随后迅速出现一系列导致脱髓鞘的变化。本研究报告称,在没有补体的情况下,反应在双折射增加阶段停止。这样,脱髓鞘过程的这个早期阶段就可以通过光学显微镜和电子显微镜进行详细检查。髓鞘变亮在暴露后数小时出现,可见于所有轴突周围,有时也见于细胞体周围。这常伴有髓鞘的突然断裂和角形髓鞘形态。电子显微镜检查显示髓鞘周期从11纳米均匀增加到22纳米。正常的双周期内线增加到四个电子致密小叶,另外两个似乎来自髓鞘或少突胶质细胞膜外表面额外电子致密层的紧密贴合。少突胶质细胞的反应是其突起大量生长,其膜紧密形成肿胀的髓鞘。神经元、星形胶质细胞和神经纤维网无变化。至少在其早期阶段,肿胀是可逆的。因此,似乎我们已经在体外分离出抗血清诱导的脱髓鞘的第一阶段,这一阶段现在可供进一步研究。

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The initial structural lesion in serum-induced demyelination in vitro.体外血清诱导脱髓鞘的初始结构损伤。
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2
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引用本文的文献

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J Neurosci Res. 2009 Mar;87(4):956-63. doi: 10.1002/jnr.21914.
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A defect of sphingolipid metabolism modifies the properties of normal appearing white matter in multiple sclerosis.鞘脂代谢缺陷改变了多发性硬化症中外观正常的白质的特性。
Brain. 2008 Nov;131(Pt 11):3092-102. doi: 10.1093/brain/awn190. Epub 2008 Sep 4.
3
A role for complement in phagocytosis of myelin.
补体在髓鞘吞噬作用中的作用。
Neurochem Res. 1997 Apr;22(4):491-8. doi: 10.1023/a:1027372129989.
4
Demyelination in experimental canine distemper virus infection: immunological, pathologic, and immunohistological studies.实验性犬瘟热病毒感染中的脱髓鞘:免疫学、病理学及免疫组织学研究
Acta Neuropathol. 1982;56(4):285-93. doi: 10.1007/BF00691260.
5
The occurrence and significance of myelin with unusually large periodicity.具有异常大周期的髓磷脂的发生及意义。
Acta Neuropathol. 1984;63(4):319-29. doi: 10.1007/BF00687340.
6
Neuropathy accompanying IgM lambda monoclonal gammopathy.伴有IgM λ单克隆丙种球蛋白病的神经病变
Acta Neuropathol. 1983;59(4):255-61. doi: 10.1007/BF00691490.
7
Double ligand ELISA technique for the estimation of antibodies to brain tissue antigens in patients with neurological disorders.用于评估神经系统疾病患者脑组织抗原抗体的双配体酶联免疫吸附测定技术。
Neurochem Res. 1985 Apr;10(4):469-81. doi: 10.1007/BF00964651.
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