Byrnes Kimberly R, Faden Alan I
Department of Neuroscience, Georgetown University Medical Center, Room EP16A, New Research Building, 3970 Reservoir Rd., NW, Washington, DC 20057, USA.
Neurochem Res. 2007 Oct;32(10):1799-807. doi: 10.1007/s11064-007-9312-2. Epub 2007 Apr 3.
Following trauma or ischemia to the central nervous system (CNS), there is a marked increase in the expression of cell cycle-related proteins. This up-regulation is associated with apoptosis of post-mitotic cells, including neurons and oligodendrocytes, both in vitro and in vivo. Cell cycle activation also induces proliferation of astrocytes and microglia, contributing to the glial scar and microglial activation with release of inflammatory factors. Treatment with cell cycle inhibitors in CNS injury models inhibits glial scar formation and neuronal cell death, resulting in substantially decreased lesion volumes and improved behavioral recovery. Here we critically review the role of cell cycle pathways in the pathophysiology of experimental stroke, traumatic brain injury and spinal cord injury, and discuss the potential of cell cycle inhibitors as neuroprotective agents.
在中枢神经系统(CNS)遭受创伤或缺血后,细胞周期相关蛋白的表达会显著增加。这种上调与有丝分裂后细胞(包括神经元和少突胶质细胞)在体外和体内的凋亡有关。细胞周期激活还会诱导星形胶质细胞和小胶质细胞增殖,促使胶质瘢痕形成以及小胶质细胞激活并释放炎性因子。在中枢神经系统损伤模型中使用细胞周期抑制剂进行治疗可抑制胶质瘢痕形成和神经元细胞死亡,从而使损伤体积大幅减小,并改善行为恢复情况。在此,我们对细胞周期通路在实验性中风、创伤性脑损伤和脊髓损伤病理生理学中的作用进行批判性综述,并讨论细胞周期抑制剂作为神经保护剂的潜力。