Beggs Simon, Salter Michael W
University of Toronto Centre for the Study of Pain, The Program in Neurosciences and Mental Health, Hospital for Sick Children, Toronto, Ont., Canada.
Brain Behav Immun. 2007 Jul;21(5):624-33. doi: 10.1016/j.bbi.2006.10.017. Epub 2006 Dec 16.
The involvement of glia, and glia-neuronal signalling in enhancing nociceptive transmission has become an area of intense scientific interest. In particular, a role has emerged for activated microglia in the development and maintenance of neuropathic pain following peripheral nerve injury. Following activation, spinal microglia proliferate and release many substances which are capable of modulating neuronal excitability within the spinal cord. Here, we the investigated the response of spinal microglia to a unilateral spared nerve injury (SNI) in terms of the quantitative increase in cell number and the spatial distribution of the increase. Design-based stereological techniques were combined with iba-1 immunohistochemistry to estimate the total number of microglia in the spinal dorsal horn in naïve and peripheral nerve-injured adult rats. In addition, by mapping the central terminals of hindlimb nerves, the somatotopic distribution of the microglial response was mapped. Following SNI there was a marked increase in the number of spinal microglia: The total number of microglia (mean+/-SD) in the dorsal horn sciatic territory of the naïve rat was estimated to be 28,591+/-2715. Following SNI the number of microglia was 82,034+/-8828. While the pattern of microglial activation generally followed somatotopic boundaries, with the majority of microglia within the territory occupied by peripherally axotomised primary afferents, some spread was seen into regions occupied by intact, 'spared' central projections of the sural nerve. This study provides a reproducible method of assaying spinal microglial dynamics following peripheral nerve injury both quantitatively and spatially.
神经胶质细胞以及神经胶质细胞与神经元之间的信号传导在增强伤害性感受传递中的作用,已成为一个备受科学界关注的领域。特别是,活化的小胶质细胞在周围神经损伤后神经性疼痛的发生和维持中所起的作用已逐渐显现。激活后,脊髓小胶质细胞会增殖并释放许多能够调节脊髓内神经元兴奋性的物质。在此,我们研究了脊髓小胶质细胞对单侧保留神经损伤(SNI)的反应,包括细胞数量的定量增加以及增加的空间分布。基于设计的体视学技术与iba - 1免疫组织化学相结合,以估计未受伤和周围神经损伤的成年大鼠脊髓背角中小胶质细胞的总数。此外,通过绘制后肢神经的中枢终末,绘制了小胶质细胞反应的躯体定位分布。SNI后,脊髓小胶质细胞数量显著增加:未受伤大鼠坐骨神经区域背角中的小胶质细胞总数(平均值±标准差)估计为28,591±2715。SNI后,小胶质细胞数量为82,034±8828。虽然小胶质细胞激活模式通常遵循躯体定位边界,大多数小胶质细胞位于外周轴突切断的初级传入纤维所占据的区域内,但也有一些扩散到了由完整的、“保留”的腓肠神经中枢投射所占据的区域。本研究提供了一种可重复的方法,用于在定量和空间上测定周围神经损伤后脊髓小胶质细胞的动态变化。