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Stem cell factor and granulocyte colony-stimulating factor promote remyelination in the chronic phase of severe traumatic brain injury.干细胞因子和粒细胞集落刺激因子促进重度创伤性脑损伤慢性期的髓鞘再生。
bioRxiv. 2023 Jan 25:2023.01.24.525450. doi: 10.1101/2023.01.24.525450.
2
Stem Cell Factor and Granulocyte Colony-Stimulating Factor Promote Remyelination in the Chronic Phase of Severe Traumatic Brain Injury.干细胞因子和粒细胞集落刺激因子促进严重创伤性脑损伤慢性期的髓鞘再生。
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SCF + G-CSF treatment in the chronic phase of severe TBI enhances axonal sprouting in the spinal cord and synaptic pruning in the hippocampus.SCF+G-CSF 治疗严重 TBI 的慢性期可增强脊髓中的轴突发芽和海马中的突触修剪。
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NF-κB is involved in brain repair by stem cell factor and granulocyte-colony stimulating factor in chronic stroke.在慢性中风中,核因子κB通过干细胞因子和粒细胞集落刺激因子参与脑修复。
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Myelin and oligodendrocyte lineage cells in white matter pathology and plasticity after traumatic brain injury.创伤性脑损伤后白质病理与可塑性中的髓磷脂和少突胶质细胞谱系细胞
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Efficacy of the coadministration of granulocyte colony-stimulating factor and stem cell factor in the activation of intrinsic cells after spinal cord injury in mice.粒细胞集落刺激因子和干细胞因子联合给药对小鼠脊髓损伤后固有细胞激活的影响。
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干细胞因子和粒细胞集落刺激因子促进重度创伤性脑损伤慢性期的髓鞘再生。

Stem cell factor and granulocyte colony-stimulating factor promote remyelination in the chronic phase of severe traumatic brain injury.

作者信息

Qiu Xuecheng, Ping Suning, Kyle Michele, Chin Lawrence, Zhao Li-Ru

出版信息

bioRxiv. 2023 Jan 25:2023.01.24.525450. doi: 10.1101/2023.01.24.525450.

DOI:10.1101/2023.01.24.525450
PMID:36747858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9900822/
Abstract

Severe traumatic brain injury (TBI) causes long-term disability and death in young adults. White matter is vulnerable to TBI damage. Demyelination is a major pathological change of white matter injury after TBI. Demyelination which is characterized by myelin sheath disruption and oligodendrocyte cell death leads to long-term neurological function deficits. Stem cell factor (SCF) and granulocyte colonyâ€"stimulating factor (G-CSF) treatments have shown neuroprotective and neurorestorative effects in the subacute and chronic phases of experimental TBI. Our previous study has revealed that combined SCF and G-CSF treatment (SCF+G-CSF) enhances myelin repair in the chronic phase of TBI. However, the long-term effect and mechanism of SCF+G-CSF-enhanced myelin repair remain unclear. In this study, we uncovered persistent and progressive myelin loss in the chronic phase of severe TBI. SCF+G-CSF treatment in the chronic phase of severe TBI enhanced remyelination in the ipsilateral external capsule and striatum. The SCF+G-CSF-enhanced myelin repair is positively correlated with the proliferation of oligodendrocyte progenitor cells in the subventricular zone. These findings reveal the therapeutic potential of SCF+G-CSF in myelin repair in the chronic phase of severe TBI and shed light on the mechanism underlying SCF+G-CSF-enhanced remyelination in chronic TBI.

摘要

严重创伤性脑损伤(TBI)会导致年轻成年人长期残疾和死亡。白质易受TBI损伤。脱髓鞘是TBI后白质损伤的主要病理变化。以髓鞘破坏和少突胶质细胞死亡为特征的脱髓鞘会导致长期神经功能缺损。干细胞因子(SCF)和粒细胞集落刺激因子(G-CSF)治疗在实验性TBI的亚急性期和慢性期已显示出神经保护和神经修复作用。我们之前的研究表明,SCF和G-CSF联合治疗(SCF+G-CSF)可增强TBI慢性期的髓鞘修复。然而,SCF+G-CSF增强髓鞘修复的长期效果和机制仍不清楚。在本研究中,我们发现严重TBI慢性期存在持续性和进行性髓鞘丢失。严重TBI慢性期的SCF+G-CSF治疗增强了同侧外囊和纹状体的髓鞘再生。SCF+G-CSF增强的髓鞘修复与脑室下区少突胶质前体细胞的增殖呈正相关。这些发现揭示了SCF+G-CSF在严重TBI慢性期髓鞘修复中的治疗潜力,并阐明了SCF+G-CSF增强慢性TBI髓鞘再生的潜在机制。