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在人类多发性硬化症模型中,对髓鞘碱性蛋白(MBP)反应性的积累使TRAIL介导的成年皮质下白质少突胶质细胞凋亡敏感化。

Accumulation of reactivity to MBP sensitizes TRAIL mediated oligodendrocyte apoptosis in adult sub cortical white matter in a model for human multiple sclerosis.

作者信息

Mir Sajad, Ali Farrah, Chauhan Deepika, Arora Rajesh, Khan Haider A

机构信息

Clinical Toxicology Laboratory, Department of Medical Elementology and Toxicology, Jamia Hamdard, Hamdard Nagar, New Delhi, 110062, India.

School of Medicine, University of Kentucky, 741 S Limestone St., Lexington, KY, 40536, USA.

出版信息

Metab Brain Dis. 2016 Apr;31(2):299-309. doi: 10.1007/s11011-015-9750-5. Epub 2015 Oct 19.

Abstract

Reactivity to myelin associated proteins is the hallmark of human multiple sclerosis (M.S) and its experimental counterparts. However, the nature of such reactivity has not been described fully. Herein, we report that myelin basic protein (MBP) reactivity accumulates in a rat model for M.S. over a period of time and sensitizes TRAIL mediated progressive oligodendrocyte apoptosis. We used active immunization by Myelin Oligodendrocyte Glycoprotein (MOG, 50 μg) to study chronic remitting relapsing encephalomyelitis in rats. A time point analysis of the progressive disease revealed cumulative accumulation of anti myelin basic protein antibodies during the disease progression with minimal change in the anti-MOG antibodies. Increased reactivity to MBP was studied to sensitize TNF related apoptosis-inducing ligand (TRAIL) and other proinflammatory cytokines in a cumulative fashion leading to the Caspase dependent apoptosis of oligodendrocytes and myelin loss. In a rescue experiment, we could limit the demyelination and prevent disease progression by neutralizing the effector, TRAIL in an early stage of the disease. This is the first study to identify the accumulation of MBP antibodies in MOG induced EAE which possibly leads to TRAIL sensitized oligodendrocyte apoptosis in the white mater of EAE rats. This finding stresses on the need to study MBP antibody titers in M.S. patients and therefore might serve as an alternate marker for progressive demyelination.

摘要

对髓鞘相关蛋白的反应性是人类多发性硬化症(MS)及其实验模型的标志。然而,这种反应性的本质尚未得到充分描述。在此,我们报告在MS大鼠模型中,髓鞘碱性蛋白(MBP)反应性会在一段时间内累积,并使TRAIL介导的少突胶质细胞进行性凋亡敏感化。我们采用髓鞘少突胶质细胞糖蛋白(MOG,50μg)主动免疫来研究大鼠的慢性缓解复发型脑脊髓炎。对进行性疾病的时间点分析显示,在疾病进展过程中抗髓鞘碱性蛋白抗体累积,而抗MOG抗体变化最小。研究发现对MBP反应性增加会以累积方式使肿瘤坏死因子相关凋亡诱导配体(TRAIL)和其他促炎细胞因子敏感化,导致少突胶质细胞的半胱天冬酶依赖性凋亡和髓鞘丢失。在一项挽救实验中,我们可以在疾病早期通过中和效应因子TRAIL来限制脱髓鞘并防止疾病进展。这是第一项确定在MOG诱导的实验性自身免疫性脑脊髓炎(EAE)中MBP抗体累积的研究,这可能导致EAE大鼠白质中TRAIL敏感化的少突胶质细胞凋亡。这一发现强调了研究MS患者MBP抗体滴度的必要性,因此可能作为进行性脱髓鞘的替代标志物。

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