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进行性多发性硬化症中神经退行性变的内源性修复与发育启发式治疗

Endogenous repair and development inspired therapy of neurodegeneration in progressive multiple sclerosis.

作者信息

Hollingsworth Ethan, Khouri Jamil, Imitola Jaime

机构信息

a Laboratory for Neural Stem Cells and Functional Neurogenetics , University Wexner Medical Center, Biomedical Research Tower , Columbus , OH , USA.

b Division of Neuroimmunology and Multiple Sclerosis and Departments of Neurology and Neuroscience. The Ohio State , University Wexner Medical Center, Biomedical Research Tower , Columbus , OH , USA.

出版信息

Expert Rev Neurother. 2017 Jun;17(6):611-629. doi: 10.1080/14737175.2017.1287564. Epub 2017 Feb 8.

Abstract

In recent years, there has been progress in understanding the etiology and immune mechanisms of multiple sclerosis (MS). however, for most, once the diagnosis is made, significant pathology is already present in the central nervous system (CNS), and in many, this leads to neurodegeneration, which accumulates in disability. although, the mechanisms of such progression are poorly understood, new data suggest lack of remyelination paired with dysfunction of neurons along with stem and progenitor cells as the basis and recent developmental studies suggest that cns repair processes share mechanisms with development. Areas covered: Here, the authors examine the neurodevelopmental processes that may be reactivated to gain a better understanding of regeneration under pathological conditions. Specifically, the authors focus on the molecular framework of these mechanisms, signaling pathways in neuron and oligodendrocyte development, and provide evidence that the activation of these processes can help us design new therapeutic avenues to halt progression. Expert commentary: Accumulating evidence indicates that there is no single mechanism of progression in MS; instead there is heterogeneity in which repair processes are perturbed. Together, this not only poses a challenge for treatment, but also at the benchside, when prioritizing which developmental targets warrant investigation in future trials.

摘要

近年来,在理解多发性硬化症(MS)的病因和免疫机制方面取得了进展。然而,对于大多数患者来说,一旦确诊,中枢神经系统(CNS)中就已经存在显著的病理变化,而且在许多患者中,这会导致神经退行性变,进而累积为残疾。尽管这种进展的机制尚不清楚,但新数据表明,髓鞘再生不足与神经元以及干细胞和祖细胞功能障碍是其基础,并且最近的发育研究表明,中枢神经系统修复过程与发育过程有共同的机制。涵盖领域:在此,作者研究了可能被重新激活的神经发育过程,以便更好地理解病理条件下的再生。具体而言,作者关注这些机制的分子框架、神经元和少突胶质细胞发育中的信号通路,并提供证据表明激活这些过程有助于我们设计新的治疗途径来阻止疾病进展。专家评论:越来越多的证据表明,MS的进展不存在单一机制;相反,修复过程受到干扰存在异质性。这不仅给治疗带来挑战,而且在实验室中,当确定哪些发育靶点值得在未来试验中研究时也带来挑战。

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