Navabi Seyedeh Parisa, Badreh Firuzeh, Khombi Shooshtari Maryam, Hajipour Somayeh, Moradi Vastegani Sadegh, Khoshnam Seyed Esmaeil
Persian Gulf Physiology Research Center, Medical Basic Sciences Research Institute, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Behbahan Faculty of Medical Sciences, Behbahan, Iran.
Heliyon. 2024 Aug 8;10(16):e35869. doi: 10.1016/j.heliyon.2024.e35869. eCollection 2024 Aug 30.
Traumatic brain injury (TBI) is one of the most causes of death and disability among people, leading to a wide range of neurological deficits. The important process of neurogenesis in the hippocampus, which includes the production, maturation and integration of new neurons, is affected by TBI due to microglia activation and the inflammatory response. During brain development, microglia are involved in forming or removing synapses, regulating the number of neurons, and repairing damage. However, in response to injury, activated microglia release a variety of pro-inflammatory cytokines, chemokines and other neurotoxic mediators that exacerbate post-TBI injury. These microglia-related changes can negatively affect hippocampal neurogenesis and disrupt learning and memory processes. To date, the intracellular signaling pathways that trigger microglia activation following TBI, as well as the effects of microglia on hippocampal neurogenesis, are poorly understood. In this review article, we discuss the effects of microglia-induced neuroinflammation on hippocampal neurogenesis following TBI, as well as the intracellular signaling pathways of microglia activation.
创伤性脑损伤(TBI)是导致人类死亡和残疾的主要原因之一,会引发多种神经功能缺损。海马体中神经发生的重要过程,包括新神经元的产生、成熟和整合,会因小胶质细胞激活和炎症反应而受到TBI的影响。在大脑发育过程中,小胶质细胞参与突触的形成或清除、调节神经元数量以及修复损伤。然而,在损伤反应中,激活的小胶质细胞会释放多种促炎细胞因子、趋化因子和其他神经毒性介质,从而加剧TBI后的损伤。这些与小胶质细胞相关的变化会对海马体神经发生产生负面影响,并扰乱学习和记忆过程。迄今为止,TBI后触发小胶质细胞激活的细胞内信号通路以及小胶质细胞对海马体神经发生的影响仍知之甚少。在这篇综述文章中,我们讨论了小胶质细胞诱导的神经炎症对TBI后海马体神经发生的影响,以及小胶质细胞激活的细胞内信号通路。