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靶向排斥导向分子A以促进多发性硬化症的再生和神经保护。

Targeting repulsive guidance molecule A to promote regeneration and neuroprotection in multiple sclerosis.

作者信息

Demicheva Elena, Cui Yi-Fang, Bardwell Philip, Barghorn Stefan, Kron Martina, Meyer Axel H, Schmidt Martin, Gerlach Björn, Leddy Mary, Barlow Eve, O'Connor Elizabeth, Choi Chee-Ho, Huang Lili, Veldman Geertruida M, Rus Horea, Shabanzadeh Alireza P, Tassew Nardos G, Monnier Philippe P, Müller Thomas, Calabresi Peter A, Schoemaker Hans, Mueller Bernhard K

出版信息

Cell Rep. 2015 Mar 24;10(11):1887-98. doi: 10.1016/j.celrep.2015.02.048.

Abstract

Repulsive guidance molecule A (RGMa) is a potent inhibitor of neuronal regeneration and a regulator of cell death, and it plays a role in multiple sclerosis (MS). In autopsy material from progressive MS patients, RGMa was found in active and chronic lesions, as well as in normal-appearing gray and white matter, and was expressed by cellular meningeal infiltrates. Levels of soluble RGMa in the cerebrospinal fluid were decreased in progressive MS patients successfully treated with intrathecal corticosteroid triamcinolone acetonide (TCA), showing functional improvements. In vitro, RGMa monoclonal antibodies (mAbs) reversed RGMa-mediated neurite outgrowth inhibition and chemorepulsion. In animal models of CNS damage and MS, RGMa antibody stimulated regeneration and remyelination of damaged nerve fibers, accelerated functional recovery, and protected the retinal nerve fiber layer as measured by clinically relevant optic coherence tomography. These data suggest that targeting RGMa is a promising strategy to improve functional recovery in MS patients.

摘要

排斥性导向分子A(RGMa)是神经元再生的强效抑制剂和细胞死亡的调节因子,在多发性硬化症(MS)中发挥作用。在进行性MS患者的尸检材料中,RGMa存在于活动性和慢性病变中,以及外观正常的灰质和白质中,并由细胞性脑膜浸润表达。成功接受鞘内注射皮质类固醇曲安奈德(TCA)治疗的进行性MS患者脑脊液中可溶性RGMa水平降低,显示出功能改善。在体外,RGMa单克隆抗体(mAb)逆转了RGMa介导的神经突生长抑制和化学排斥。在中枢神经系统损伤和MS的动物模型中,RGMa抗体刺激受损神经纤维的再生和髓鞘再生,加速功能恢复,并通过临床相关的光学相干断层扫描测量保护视网膜神经纤维层。这些数据表明,靶向RGMa是改善MS患者功能恢复的一种有前景的策略。

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