骨髓间充质干细胞衍生外泌体对脊髓损伤的修复:基于大鼠模型的系统综述和荟萃分析

IF 3.5 3区 医学 Q2 NEUROSCIENCES Frontiers in Molecular Neuroscience Pub Date : 2024-08-07 DOI:10.3389/fnmol.2024.1448777
Zhongduo Ye, Yukun Zheng, Ningning Li, Huaibin Zhang, Qiangqiang Li, Xiong Wang
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The results indicated that BMSCs-Exo significantly improved the BBB score in SCI rats (WMD = 3.47, 95% CI [3.31, 3.63]), inhibited the expression of the pro-inflammatory cytokine TNF-<jats:italic>α</jats:italic> (SMD = -3.12, 95% CI [−3.57, −2.67]), and promoted the expression of anti-inflammatory cytokines IL-10 (SMD = 2.76, 95% CI [1.88, 3.63]) and TGF-<jats:italic>β</jats:italic> (SMD = 3.89, 95% CI [3.02, 4.76]). Additionally, BMSCs-Exo significantly reduced apoptosis levels (SMD = −4.52, 95% CI [−5.14, −3.89]), promoted the expression of axonal regeneration markers NeuN cells/field (SMD = 3.54, 95% CI [2.65, 4.42]), NF200 (SMD = 4.88, 95% CI [3.70, 6.05]), and the number of Nissl bodies (SMD = 1.89, 95% CI [1.13, 2.65]), and decreased the expression of astrogliosis marker GFAP (SMD = −5.15, 95% CI [−6.47, −3.82]). 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引用次数: 0

摘要

本研究旨在系统评估骨髓间充质干细胞衍生的外泌体(BMSCs-Exo)在改善脊髓损伤(SCI)方面的疗效,以降低从动物实验到临床应用的转化差异风险。两名研究人员独立筛选文献、提取数据并评估研究质量。结果共纳入 30 项研究。结果表明,BMSCs-Exo 能显著改善 SCI 大鼠的 BBB 评分(WMD = 3.47,95% CI [3.31,3.63]),抑制促炎细胞因子 TNF-α 的表达(SMD = -3.12,95% CI [-3.57,-2.67]),促进抗炎细胞因子 IL-10 (SMD = 2.76,95% CI [1.88,3.63])和 TGF-β (SMD = 3.89,95% CI [3.02,4.76])的表达。此外,BMSCs-Exo 能显著降低细胞凋亡水平(SMD = -4.52,95% CI [-5.14, -3.89]),促进轴突再生标记 NeuN 细胞/场(SMD = 3.54,95% CI [2.65, 4.42])、NF200(SMD = 4.88,95% CI [3.70,6.05])和 Nissl 体数量(SMD = 1.89,95% CI [1.13,2.65])的表达,并降低星形胶质细胞标志物 GFAP(SMD = -5.15,95% CI [-6.47,-3.82])的表达。结论 BMSCs-Exo 可通过调节炎症反应、减少细胞凋亡、抑制星形胶质细胞增生和促进轴突再生,显著改善 SCI 大鼠的运动功能。然而,目前动物实验中存在的选择、表现和检测偏差可能会影响本研究的证据质量。
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Repair of spinal cord injury by bone marrow mesenchymal stem cell-derived exosomes: a systematic review and meta-analysis based on rat models
ObjectiveThis study aims to systematically evaluate the efficacy of bone marrow mesenchymal stem cell-derived exosomes (BMSCs-Exo) in improving spinal cord injury (SCI) to mitigate the risk of translational discrepancies from animal experiments to clinical applications.MethodsWe conducted a comprehensive literature search up to March 2024 using PubMed, Embase, Web of Science, and Scopus databases. Two researchers independently screened the literature, extracted data, and assessed the quality of the studies. Data analysis was performed using STATA16 software.ResultsA total of 30 studies were included. The results indicated that BMSCs-Exo significantly improved the BBB score in SCI rats (WMD = 3.47, 95% CI [3.31, 3.63]), inhibited the expression of the pro-inflammatory cytokine TNF-α (SMD = -3.12, 95% CI [−3.57, −2.67]), and promoted the expression of anti-inflammatory cytokines IL-10 (SMD = 2.76, 95% CI [1.88, 3.63]) and TGF-β (SMD = 3.89, 95% CI [3.02, 4.76]). Additionally, BMSCs-Exo significantly reduced apoptosis levels (SMD = −4.52, 95% CI [−5.14, −3.89]), promoted the expression of axonal regeneration markers NeuN cells/field (SMD = 3.54, 95% CI [2.65, 4.42]), NF200 (SMD = 4.88, 95% CI [3.70, 6.05]), and the number of Nissl bodies (SMD = 1.89, 95% CI [1.13, 2.65]), and decreased the expression of astrogliosis marker GFAP (SMD = −5.15, 95% CI [−6.47, −3.82]). The heterogeneity among studies was primarily due to variations in BMSCs-Exo transplantation doses, with efficacy increasing with higher doses.ConclusionBMSCs-Exo significantly improved motor function in SCI rats by modulating inflammatory responses, reducing apoptosis, inhibiting astrogliosis, and promoting axonal regeneration. However, the presence of selection, performance, and detection biases in current animal experiments may undermine the quality of evidence in this study.
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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