Department of Spine Surgery, The Sixth Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Front Immunol. 2023 Jan 12;13:1094925. doi: 10.3389/fimmu.2022.1094925. eCollection 2022.
High mobility group box 1 (HMGB1) has dual functions as a nonhistone nucleoprotein and an extracellular inflammatory cytokine. In the resting state, HMGB1 is mainly located in the nucleus and regulates key nuclear activities. After spinal cord injury, HMGB1 is rapidly expressed by neurons, microglia and ependymal cells, and it is either actively or passively released into the extracellular matrix and blood circulation; furthermore, it also participates in the pathophysiological process of spinal cord injury. HMGB1 can regulate the activation of M1 microglia, exacerbate the inflammatory response, and regulate the expression of inflammatory factors through Rage and TLR2/4, resulting in neuronal death. However, some studies have shown that HMGB1 is beneficial for the survival, regeneration and differentiation of neurons and that it promotes the recovery of motor function. This article reviews the specific timing of secretion and translocation, the release mechanism and the role of HMGB1 in spinal cord injury. Furthermore, the role and mechanism of HMGB1 in spinal cord injury and, the challenges that still need to be addressed are identified, and this work will provide a basis for future studies.
高迁移率族蛋白 B1(HMGB1)具有非组蛋白核蛋白和细胞外炎性细胞因子的双重功能。在静息状态下,HMGB1 主要位于细胞核内,调节关键的核活性。脊髓损伤后,HMGB1 被神经元、小胶质细胞和室管膜细胞迅速表达,并主动或被动释放到细胞外基质和血液循环中;此外,它还参与脊髓损伤的病理生理过程。HMGB1 可以通过 Rage 和 TLR2/4 调节 M1 小胶质细胞的激活,加剧炎症反应,并调节炎症因子的表达,导致神经元死亡。然而,一些研究表明,HMGB1 有利于神经元的存活、再生和分化,并促进运动功能的恢复。本文综述了 HMGB1 在脊髓损伤中的具体分泌和转位时间、释放机制以及作用,明确了 HMGB1 在脊髓损伤中的作用和机制,以及仍需解决的挑战,为今后的研究提供了依据。