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[细胞因子与周围神经病变]

[Cytokines and peripheral neuropathies].

作者信息

Créange A, Lefaucheur J P, Authier F J, Gherardi R K

机构信息

Groupe d'Etudes et de Recherches sur le Muscle et le Nerf (GERMEN), Faculté de Médecine de Créteil, Hôpital Henri Mondor.

出版信息

Rev Neurol (Paris). 1998 Apr;154(3):208-16.

PMID:9773044
Abstract

Cytokines are polypeptides produced by various cells, with key-roles in regulation of immune response, inflammation and hematopoiesis. Cytokine-producing cells in peripheral nerve include resident and recruited macrophages, lymphocytes, and likely mastocytes, Schwann cells, and probably neurons. Cytokines are instrumental in pathogenesis of peripheral neuropathies during nerve lesions and tissue repair. Tumor necrosis factor-alpha (TNF-alpha) injection into nerve induces Wallerian degeneration. In contrast, interleukin-1 (IL-1) promotes detersion by scavenger macrophages, and increased synthesis of neurotrophic factor (nerve growth factor--NGF--and leukemia inhibitory factor--LIF). Neurotrophic cytokines IL-6, LIF and transforming growth factor-beta 1 (TGF-beta 1) are overexpressed in nerve after experimental axotomy and promote axonal growth until axon/Schwann cell contact. In the course of inflammatory demyelinating neuropathies, proinflammatory cytokines induce vascular permeability and breakdown of blood nerve barrier (TNF-alpha, vascular endothelial growth factor/vascular permeability factor--VEGF/VPF), favor leukocyte transmigration into nerve, induce activation and proliferation of lymphocytes (IL-1, IL-2) and macrophages (gamma-interferon--IFN-gamma), and have a direct myelinotoxic activity (TNF-alpha and TNF-beta). In addition, the inflammatory process is likely favored by downregulation of the anti-inflammatory cytokine TGF-beta 1.

摘要

细胞因子是由多种细胞产生的多肽,在免疫反应、炎症和造血调节中起关键作用。外周神经中产生细胞因子的细胞包括常驻和募集的巨噬细胞、淋巴细胞,可能还有肥大细胞、施万细胞,或许还有神经元。细胞因子在神经损伤和组织修复过程中外周神经病变的发病机制中起重要作用。向神经内注射肿瘤坏死因子-α(TNF-α)可诱导沃勒变性。相比之下,白细胞介素-1(IL-1)可促进清道夫巨噬细胞的清除作用,并增加神经营养因子(神经生长因子-NGF-和白血病抑制因子-LIF)的合成。神经营养细胞因子IL-6、LIF和转化生长因子-β1(TGF-β1)在实验性轴突切断后的神经中过度表达,并促进轴突生长直至轴突/施万细胞接触。在炎性脱髓鞘性神经病的过程中,促炎细胞因子可诱导血管通透性增加和血神经屏障破坏(TNF-α、血管内皮生长因子/血管通透性因子-VEGF/VPF),有利于白细胞迁移到神经中,诱导淋巴细胞(IL-1、IL-2)和巨噬细胞(γ-干扰素-IFN-γ)的活化和增殖,并具有直接的髓鞘毒性活性(TNF-α和TNF-β)。此外,抗炎细胞因子TGF-β1的下调可能有利于炎症过程。

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[Cytokines and peripheral neuropathies].[细胞因子与周围神经病变]
Rev Neurol (Paris). 1998 Apr;154(3):208-16.
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[Cytokines and inflammation].[细胞因子与炎症]
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