Warwick Rebekah A, Ledgerwood Craig J, Brenner Talma, Hanani Menachem
Laboratory of Experimental Surgery, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem 91240, Israel.
Laboratory of Experimental Surgery, Hadassah-Hebrew University Medical Center, Mount Scopus, Jerusalem 91240, Israel.
Neurosci Lett. 2014 May 21;569:59-62. doi: 10.1016/j.neulet.2014.03.033. Epub 2014 Mar 29.
Pain is a serious and common problem with patients suffering from multiple sclerosis (MS). Very little has been done to investigate the peripheral mechanisms of pain in MS. Here we used a mouse model of experimental autoimmune encephalomyelitis (EAE) to investigate the possible contribution of satellite glial cells (SGCs) to pain in MS. EAE mice had reduced pain thresholds 10 days after disease induction. We examined dorsal root ganglia and found increased expression of glial fibrillary acidic protein in SGCs, a marker of SGC activation, and increased coupling among SGCs, a known component of activated SGCs. Activated SGCs have previously been shown to contribute to pain in other classical neuropathic pain models, suggesting that pain in multiple sclerosis has a peripheral component.
疼痛是多发性硬化症(MS)患者面临的一个严重且常见的问题。目前针对MS疼痛的外周机制研究甚少。在此,我们使用实验性自身免疫性脑脊髓炎(EAE)小鼠模型来探究卫星神经胶质细胞(SGCs)在MS疼痛中可能发挥的作用。疾病诱导后10天,EAE小鼠的疼痛阈值降低。我们检查了背根神经节,发现SGCs中胶质纤维酸性蛋白的表达增加,这是SGC激活的标志物,并且SGCs之间的耦合增加,这是活化SGCs的一个已知组成部分。先前已证明活化的SGCs在其他经典神经性疼痛模型中会导致疼痛,这表明多发性硬化症中的疼痛存在外周因素。