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皮质再髓鞘化在多发性硬化症中是异质性的。

Cortical Remyelination Is Heterogeneous in Multiple Sclerosis.

作者信息

Strijbis Eva M M, Kooi Evert-Jan, van der Valk Paul, Geurts Jeroen J G

机构信息

From the Department of Neurology (EMMS), Department of Anatomy & Neurosciences, Section of Clinical Neuroscience (EMMS, E-JK, JJGG), VU University Medical Center, De Boelelaan 1118, 1081 HV Amsterdam, The Netherlands; and Department of Pathology (Neuropathology), VU University Medical Center, De Boelelaan 1117, 1081 HV Amsterdam, The Netherlands (E-JK, PvdV).

出版信息

J Neuropathol Exp Neurol. 2017 May 1;76(5):390-401. doi: 10.1093/jnen/nlx023.

Abstract

Cortical lesions (CLs) are an important component of multiple sclerosis (MS) pathology; they correlate better with physical disability and cognitive impairment than white matter lesions (WMLs). Because remyelination can be extensive in CLs, we quantified remyelination in gray matter (GM) and white matter (WM), addressing oligodendrocyte (OGD) maturation state and clinical relevance of remyelination. Brain tissue samples from 21 chronic MS patients were immunohistochemically stained for myelin proteolipid protein, Olig2, which is strongly expressed in OGD precursor cells (OPCs), but weakly expressed in mature OGDs and other OGD markers. Sections were scored for the presence of normal-appearing WM and GM, de- and remyelination, and OPC and OGD cell counts. Remyelination was significantly more extensive in CLs than in WMLs with a trend toward more GM remyelination in primary progressive MS (PPMS) vs relapse-onset MS patients. More OPCs were found in remyelinated and nonremyelinated CLs vs remyelinated WMLs and nonremyelinated WMLs. Thus, there is more remyelination in the GM than in the WM in MS patient brains, with a trend toward more remyelination in those with PPMS. There does not seem to be a significant OPC recruitment failure in the GM, which casts new light on the process of remyelination failure.

摘要

皮质病灶(CLs)是多发性硬化症(MS)病理的重要组成部分;与白质病灶(WMLs)相比,它们与身体残疾和认知障碍的相关性更强。由于CLs中可出现广泛的髓鞘再生,我们对白质(WM)和灰质(GM)中的髓鞘再生进行了量化,探讨了少突胶质细胞(OGD)的成熟状态以及髓鞘再生的临床相关性。对21例慢性MS患者的脑组织样本进行免疫组织化学染色,检测髓磷脂蛋白脂蛋白、Olig2,Olig2在少突胶质前体细胞(OPCs)中强烈表达,但在成熟少突胶质细胞和其他少突胶质细胞标志物中弱表达。对切片进行评分,评估正常外观的WM和GM的存在情况、脱髓鞘和髓鞘再生情况以及OPC和少突胶质细胞计数。CLs中的髓鞘再生明显比WMLs更广泛,原发性进展型MS(PPMS)患者的GM髓鞘再生比复发型MS患者有更多的趋势。与髓鞘再生的WMLs和未髓鞘再生的WMLs相比,在髓鞘再生和未髓鞘再生的CLs中发现了更多的OPCs。因此,MS患者大脑中GM的髓鞘再生比WM更多,PPMS患者的髓鞘再生有更多的趋势。GM中似乎不存在明显的OPC募集失败,这为髓鞘再生失败的过程提供了新的线索。

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