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周围神经系统中的髓鞘与巨噬细胞:创伤与疾病中的密切关系。

Myelin and macrophages in the PNS: An intimate relationship in trauma and disease.

作者信息

Klein Dennis, Martini Rudolf

机构信息

University Hospital Würzburg, Department of Neurology, Developmental Neurobiology, Josef-Schneider Str. 11, 97080 Würzburg, Germany.

University Hospital Würzburg, Department of Neurology, Developmental Neurobiology, Josef-Schneider Str. 11, 97080 Würzburg, Germany.

出版信息

Brain Res. 2016 Jun 15;1641(Pt A):130-138. doi: 10.1016/j.brainres.2015.11.033. Epub 2015 Nov 26.

Abstract

Macrophages of the peripheral nervous system belong to the so-called tissue macrophages, with multiple functions during injury and disease. Their origin during ontogeny has not yet been completely resolved, but it is clear that upon injury and disease conditions, they are supplemented by hematopoietic derivatives. In the peripheral nervous system, the most abundantly investigated scenario in which resident and infiltrating macrophages are involved is the so-called "Wallerian degeneration", a complex degenerative process where macrophages exhibit mostly beneficial functions by phagocytosing myelin and axonal remnants. Of special interest is the implication of macrophages in inflammatory nerve diseases, like acute Guillain-Barré syndromes and its permanent variant, chronic inflammatory demyelinating polyneuropathy, where macrophages are supposed to be substantial (co-)mediators of the diseases. In inherited peripheral neuropathies nerve macrophages possess a clear disease-amplifying function. In the corresponding animal models, a coordinated interplay between mutant Schwann cells, macrophages, endoneurial fibroblasts and the target structure, myelin, emerged. Along this process, a newly discovered disease mechanism mediated by macrophages is the dedifferentiation of myelinating Schwann cells. As macrophages are amplifiers of the genetically-mediated, non-curable diseases, targeting the mechanisms of their activation might be a promising strategy to treat these disorders. This article is part of a Special Issue entitled SI: Myelin Evolution.

摘要

外周神经系统的巨噬细胞属于所谓的组织巨噬细胞,在损伤和疾病过程中具有多种功能。它们在个体发育过程中的起源尚未完全明确,但很明显,在损伤和疾病状态下,造血来源的细胞会补充到其中。在外周神经系统中,驻留和浸润巨噬细胞参与的研究最为充分的情况是所谓的“沃勒变性”,这是一个复杂的退行性过程,在此过程中巨噬细胞通过吞噬髓鞘和轴突残端发挥主要的有益作用。特别值得关注的是巨噬细胞在炎性神经疾病中的作用,如急性吉兰 - 巴雷综合征及其慢性变异型慢性炎性脱髓鞘性多发性神经病,在这些疾病中巨噬细胞被认为是主要的(共同)致病介质。在遗传性周围神经病中,神经巨噬细胞具有明确的疾病放大功能。在相应的动物模型中,突变的施万细胞、巨噬细胞、神经内膜成纤维细胞和靶结构髓鞘之间出现了协调的相互作用。在此过程中,巨噬细胞介导的一种新发现的疾病机制是髓鞘形成的施万细胞去分化。由于巨噬细胞是遗传介导的、不可治愈疾病的放大器,针对其激活机制可能是治疗这些疾病的一种有前景的策略。本文是名为“髓鞘进化”特刊的一部分。

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