Department of Anesthesiology, Jinling Hospital, Affiliated Hospital of Nanjing Medical University, Nanjing, PR China.
Department of Anesthesiology, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, PR China.
Int Rev Immunol. 2024;43(5):326-339. doi: 10.1080/08830185.2024.2344170. Epub 2024 Apr 25.
Research on the relationship between macrophages and neuropathic pain has flourished in the past two decades. It has long been believed that macrophages are strong immune effector cells that play well-established roles in tissue homeostasis and lesions, such as promoting the initiation and progression of tissue injury and improving wound healing and tissue remodeling in a variety of pathogenesis-related diseases. They are also heterogeneous and versatile cells that can switch phenotypically/functionally in response to the micro-environment signals. Apart from microglia (resident macrophages of both the spinal cord and brain), which are required for the neuropathic pain processing of the CNS, neuropathic pain signals in PNS are influenced by the interaction of tissue-resident macrophages and BM infiltrating macrophages with primary afferent neurons. And the current review looks at new evidence that suggests sexual dimorphism in neuropathic pain are caused by variations in the immune system, notably macrophages, rather than the neurological system.
在过去的二十年中,巨噬细胞与神经病理性疼痛之间的关系的研究蓬勃发展。长期以来,人们一直认为巨噬细胞是强大的免疫效应细胞,在组织稳态和损伤中发挥着明确的作用,例如促进组织损伤的发生和进展,并在多种与发病机制相关的疾病中改善伤口愈合和组织重塑。它们还是异质性和多功能的细胞,可以根据微环境信号在表型/功能上发生转变。除了小胶质细胞(中枢神经系统和大脑中的固有巨噬细胞),小胶质细胞对于中枢神经系统的神经病理性疼痛处理是必需的之外,周围神经系统中的神经病理性疼痛信号还受到组织驻留巨噬细胞和 BM 浸润巨噬细胞与初级传入神经元相互作用的影响。本综述着眼于新的证据表明,神经病理性疼痛的性别二态性是由免疫系统的变化引起的,特别是巨噬细胞,而不是神经系统。