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本文引用的文献

1
Macrophage-Derived Vascular Endothelial Growth Factor-A Is Integral to Neuromuscular Junction Reinnervation after Nerve Injury.巨噬细胞衍生的血管内皮生长因子 A 是神经损伤后神经肌肉接点再支配所必需的。
J Neurosci. 2020 Dec 9;40(50):9602-9616. doi: 10.1523/JNEUROSCI.1736-20.2020. Epub 2020 Nov 6.
2
Incidence of Nerve Injury After Extremity Trauma in the United States.美国四肢创伤后神经损伤的发生率。
Hand (N Y). 2022 Jul;17(4):615-623. doi: 10.1177/1558944720963895. Epub 2020 Oct 21.
3
The CCL2/CCR2 axis is critical to recruiting macrophages into acellular nerve allograft bridging a nerve gap to promote angiogenesis and regeneration.CCL2/CCR2 轴对于招募巨噬细胞进入去细胞神经移植物桥接神经间隙以促进血管生成和再生至关重要。
Exp Neurol. 2020 Sep;331:113363. doi: 10.1016/j.expneurol.2020.113363. Epub 2020 May 23.
4
Profiling peripheral nerve macrophages reveals two macrophage subsets with distinct localization, transcriptome and response to injury.分析周围神经巨噬细胞揭示了两种具有不同定位、转录组和对损伤反应的巨噬细胞亚群。
Nat Neurosci. 2020 May;23(5):676-689. doi: 10.1038/s41593-020-0618-6. Epub 2020 Apr 13.
5
Acute and long-term costs of 268 peripheral nerve injuries in the upper extremity.上肢 268 例周围神经损伤的急性和长期费用。
PLoS One. 2020 Apr 6;15(4):e0229530. doi: 10.1371/journal.pone.0229530. eCollection 2020.
6
Perisynaptic Schwann cells phagocytose nerve terminal debris in a mouse model of Guillain-Barré syndrome.施万细胞吞噬神经末梢碎片在格林-巴利综合征的小鼠模型中。
J Peripher Nerv Syst. 2020 Jun;25(2):143-151. doi: 10.1111/jns.12373. Epub 2020 Apr 20.
7
Ultrastructural mechanisms of macrophage-induced demyelination in Guillain-Barré syndrome.巨细胞病毒感染与吉兰-巴雷综合征的相关性研究进展
J Neurol Neurosurg Psychiatry. 2020 Jun;91(6):650-659. doi: 10.1136/jnnp-2019-322479. Epub 2020 Apr 3.
8
Gpr126/Adgrg6 contributes to the terminal Schwann cell response at the neuromuscular junction following peripheral nerve injury.Gpr126/Adgrg6 有助于外周神经损伤后神经肌肉接头处施万细胞的终末反应。
Glia. 2020 Jun;68(6):1182-1200. doi: 10.1002/glia.23769. Epub 2019 Dec 24.
9
Indirect Cost of Traumatic Brachial Plexus Injuries in the United States.美国创伤性臂丛神经损伤的间接成本。
J Bone Joint Surg Am. 2019 Aug 21;101(16):e80. doi: 10.2106/JBJS.18.00658.
10
What is Normal? Neuromuscular junction reinnervation after nerve injury.正常是什么?神经损伤后的神经肌肉接头再支配。
Muscle Nerve. 2019 Nov;60(5):604-612. doi: 10.1002/mus.26654. Epub 2019 Aug 23.

巨噬细胞在外周神经系统损伤和病理中的作用:神经肌肉接头恢复的盟友。

Macrophage roles in peripheral nervous system injury and pathology: Allies in neuromuscular junction recovery.

机构信息

Washington University School of Medicine, St. Louis, MO, United States of America.

Division of Plastic Surgery, Department of Surgery, Washington University School of Medicine, St. Louis, MO, United States of America.

出版信息

Mol Cell Neurosci. 2021 Mar;111:103590. doi: 10.1016/j.mcn.2021.103590. Epub 2021 Jan 8.

DOI:10.1016/j.mcn.2021.103590
PMID:33422671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8235592/
Abstract

Peripheral nerve injuries remain challenging to treat despite extensive research on reparative processes at the injury site. Recent studies have emphasized the importance of immune cells, particularly macrophages, in recovery from nerve injury. Macrophage plasticity enables numerous functions at the injury site. At early time points, macrophages perform inflammatory functions, but at later time points, they adopt pro-regenerative phenotypes to support nerve regeneration. Research has largely been limited, however, to the injury site. The neuromuscular junction (NMJ), the synapse between the nerve terminal and end target muscle, has received comparatively less attention, despite the importance of NMJ reinnervation for motor recovery. Macrophages are present at the NMJ following nerve injury. Moreover, in denervating diseases, such as amyotrophic lateral sclerosis (ALS), macrophages may also play beneficial roles at the NMJ. Evidence of positive macrophages roles at the injury site after peripheral nerve injury and at the NMJ in denervating pathologies suggest that macrophages may promote NMJ reinnervation. In this review, we discuss the intersection of nerve injury and immunity, with a focus on macrophages.

摘要

尽管对损伤部位的修复过程进行了广泛的研究,但周围神经损伤的治疗仍然具有挑战性。最近的研究强调了免疫细胞(尤其是巨噬细胞)在神经损伤恢复中的重要性。巨噬细胞的可塑性使其能够在损伤部位发挥多种功能。在早期,巨噬细胞发挥炎症功能,但在后期,它们会采用促再生表型来支持神经再生。然而,研究主要局限于损伤部位。神经肌肉接头(NMJ)是神经末梢和终末靶肌肉之间的突触,尽管 NMJ 再支配对于运动恢复很重要,但 NMJ 受到的关注相对较少。巨噬细胞存在于神经损伤后的 NMJ 中。此外,在神经退行性疾病(如肌萎缩侧索硬化症,ALS)中,巨噬细胞在 NMJ 中也可能发挥有益作用。周围神经损伤后损伤部位和去神经病变中的 NMJ 中存在的巨噬细胞发挥积极作用的证据表明,巨噬细胞可能促进 NMJ 再支配。在这篇综述中,我们讨论了神经损伤和免疫之间的交叉点,重点是巨噬细胞。