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首页> 外文期刊>Scientific reports. >Interleukin-1β pre-treated bone marrow stromal cells alleviate neuropathic pain through CCL7-mediated inhibition of microglial activation in the spinal cord
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Interleukin-1β pre-treated bone marrow stromal cells alleviate neuropathic pain through CCL7-mediated inhibition of microglial activation in the spinal cord

机译:白细胞介素-1β预处理的骨髓基质细胞通过CCL7介导的脊髓微胶质活化抑制神经性疼痛

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Although neuropathic pain is one of the most intractable diseases, recent studies indicate that systemic or local injection of bone marrow stromal cells (BMSCs) decreases pro-inflammatory cytokines release and alleviates neuropathic pain. However, it is still not clear whether pre-treated BMSCs have a strong anti-inflammatory and/or analgesia effect. Using the spinal nerve ligation model of neuropathic pain, IL-1β pre-treated BMSCs (IL-1β-BMSCs) were injected into rats followed by SNL in order to determine possible effects. Results indicated that IL-1β-BMSCs were more efficacious in both amelioration of neuropathic pain and inhibition of microglia activation. Specifically, microglia inhibition was found to be mediated by chemokine C-C motif ligand 7 (CCL7) but not CCL2. Results also showed that IL-1β-BMSCs had a stronger inhibitory effect on astrocyte activation as well as CCL7 release, which was found to be mediated by IL-10 not transforming growth factor-β1. In addition, we also found directional migration of IL-1β-BMSCs was mediated by inceased C-X-C motif chemokine ligand (CXCL) 13 expression following SNL. In conclusion, our results indicated IL-1β-BMSCs could inhibit microglia activation and neuropathic pain by decreasing CCL7 level in spinal cord.
机译:虽然神经性疼痛是最顽固的疾病之一,但最近的研究表明,全身或局部注射骨髓基质细胞(BMSCs)降低促炎细胞因子释放并减轻神经性疼痛。然而,仍然尚不清楚预处理的BMSCs是否具有强烈的抗炎和/或镇痛作用。使用神经性疼痛的脊神经连接模型,将IL-1β预处理的BMSCs(IL-1β-BMSCs)注入大鼠后,然后是SNL以确定可能的影响。结果表明,IL-1β-BMSC在神经性疼痛和抑制微血花症激活的改善方面更有效。具体地,发现小胶质细胞抑制由趋化因子C-C基序配体7(CCL7)介导但不是CCL2。结果还表明,IL-1β-BMSCs对星形胶质细胞活化以及CCL7释放具有更强的抑制作用,发现该释放被发现由IL-10未转化生长因子-β1介导。此外,我们还发现IL-1β-BMSCs的定向迁移通过灭活的C-X-C型趋化因子配体(CXCL)13如SN1表达介导。总之,我们的结果表明IL-1β-BMSCs可以通过降低脊髓中的CCl7水平来抑制小凝血性活化和神经性疼痛。

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