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神经炎症、骨髓干细胞与慢性疼痛

Neuroinflammation, Bone Marrow Stem Cells, and Chronic Pain.

作者信息

Huh Yul, Ji Ru-Rong, Chen Gang

机构信息

Department of Anesthesiology, Duke University Medical Center, Durham, NC, United States.

Department of Neurobiology, Duke University Medical Center, Durham, NC, United States.

出版信息

Front Immunol. 2017 Aug 21;8:1014. doi: 10.3389/fimmu.2017.01014. eCollection 2017.

Abstract

Current treatments for chronic pain, such as inflammatory pain, neuropathic pain, and cancer pain are insufficient and cause severe side effects. Mounting evidence suggests that neuroinflammation in the peripheral and central nervous system (PNS and CNS) plays a pivotal role in the genesis and maintenance of chronic pain. Characteristic features of neuroinflammation in chronic pain conditions include infiltration of immune cells into the PNS [e.g., the sciatic nerve and dorsal root ganglion (DRG)], activation of glial cells such as microglia and astrocytes in the CNS (spinal cord and brain), and production and secretion of pro-inflammatory cytokines and chemokines [TNF, interleukin (IL)-1β, IL-6, CCL2, and CXCL1]. Recent studies suggest that bone marrow stem cells or bone marrow stromal cells (BMSCs) produce powerful analgesic effects in animal models of inflammatory pain, neuropathic pain, and cancer pain. We recently demonstrated that intrathecal injection of BMSCs resulted in a long-term relief of neuropathic pain for several weeks after peripheral nerve injury. Strikingly, this analgesic effect is mediated by the anti-inflammatory cytokine transforming growth factor beta secreted from BMSCs. Additionally, BMSCs exhibit potent modulation of neuroinflammation, by inhibiting monocyte infiltration, glial activation, and cytokine/chemokine production in the DRG and spinal cord. Thus, BMSCs control chronic pain by regulation of neuroinflammation in the PNS and CNS paracrine signaling. In this review, we discuss the similar results from different laboratories of remarkable anti-nociceptive efficacy of BMSCs in animal and clinical studies. We also discuss the mechanisms by which BMSCs control neuroinflammation and chronic pain and how these cells specifically migrate to damaged tissues.

摘要

目前针对慢性疼痛(如炎性疼痛、神经性疼痛和癌痛)的治疗方法并不充分,且会引发严重的副作用。越来越多的证据表明,外周和中枢神经系统(PNS和CNS)中的神经炎症在慢性疼痛的发生和维持中起关键作用。慢性疼痛状态下神经炎症的特征包括免疫细胞浸润到PNS(如坐骨神经和背根神经节)、CNS(脊髓和脑)中的小胶质细胞和星形胶质细胞等胶质细胞激活,以及促炎细胞因子和趋化因子(TNF、白细胞介素-1β、IL-6、CCL2和CXCL1)的产生和分泌。最近的研究表明,骨髓干细胞或骨髓基质细胞(BMSCs)在炎性疼痛、神经性疼痛和癌痛的动物模型中产生强大的镇痛作用。我们最近证明鞘内注射BMSCs可在周围神经损伤后数周内长期缓解神经性疼痛。令人惊讶的是,这种镇痛作用是由BMSCs分泌的抗炎细胞因子转化生长因子β介导的。此外,BMSCs通过抑制DRG和脊髓中的单核细胞浸润、胶质细胞激活以及细胞因子/趋化因子产生,对神经炎症表现出有效的调节作用。因此,BMSCs通过调节PNS和CNS中的神经炎症旁分泌信号来控制慢性疼痛。在这篇综述中,我们讨论了不同实验室在动物和临床研究中关于BMSCs显著的抗伤害感受功效的类似结果,并讨论了BMSCs控制神经炎症和慢性疼痛的机制以及这些细胞如何特异性迁移到受损组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8673/5567062/18e12c6008e9/fimmu-08-01014-g001.jpg

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