Department of Pediatrics, Washington University in St. Louis School of Medicine, Campus Box 8208, One Children's Place, St. Louis, MO, 63110, USA.
Neurotherapeutics. 2023 Oct;20(6):1859-1874. doi: 10.1007/s13311-023-01443-8. Epub 2023 Sep 28.
Traumatic brain injury (TBI) can result in axonal loss and demyelination, leading to persistent damage in the white matter. Demyelinated axons are vulnerable to pathologies related to an abnormal myelin structure that expose neurons to further damage. Oligodendrocyte progenitor cells (OPCs) mediate remyelination after recruitment to the injury site. Often this process is inefficient due to inadequate OPC proliferation. To date, no effective treatments are currently available to stimulate OPC proliferation in TBI. Recombinant human erythropoietin (rhEPO) is a pleiotropic neuroprotective cytokine, and its receptor is present in all stages of oligodendroglial lineage cell differentiation. Therefore, we hypothesized that rhEPO administration would enhance remyelination after TBI through the modulation of OPC response. Utilizing a murine model of controlled cortical impact and a primary OPC culture in vitro model, we characterized the impact of rhEPO on remyelination and proliferation of oligodendrocyte lineage cells. Myelin black gold II staining of the peri-contusional corpus callosum revealed an increase in myelinated area in association with an increase in BrdU-positive oligodendrocytes in injured mice treated with rhEPO. Furthermore, morphological analysis of OPCs showed a decrease in process length in rhEPO-treated animals. RhEPO treatment increased OPC proliferation after in vitro CSPG exposure. Erythropoietin receptor (EPOr) gene knockdown using siRNA prevented rhEPO-induced OPC proliferation, demonstrating that the rhEPO effect on OPC response is EPOr activation dependent. Together, our findings demonstrate that rhEPO administration may promote myelination by increasing oligodendrocyte lineage cell proliferation after TBI.
创伤性脑损伤 (TBI) 可导致轴突损失和脱髓鞘,从而导致白质持续损伤。脱髓鞘轴突易受到与异常髓鞘结构相关的病理学影响,从而使神经元进一步受损。少突胶质前体细胞 (OPC) 在募集到损伤部位后介导髓鞘再生。通常,由于 OPC 增殖不足,该过程效率低下。迄今为止,尚无有效的治疗方法可刺激 TBI 中的 OPC 增殖。重组人促红细胞生成素 (rhEPO) 是一种多效性神经保护细胞因子,其受体存在于少突胶质谱系细胞分化的所有阶段。因此,我们假设 rhEPO 给药通过调节 OPC 反应来增强 TBI 后的髓鞘再生。利用控制皮质撞击的小鼠模型和体外原代 OPC 培养模型,我们描述了 rhEPO 对髓鞘再生和少突胶质谱系细胞增殖的影响。损伤小鼠给予 rhEPO 治疗后,胼胝体损伤区周围的髓鞘黑金 II 染色显示髓鞘面积增加,与 BrdU 阳性少突胶质细胞增加相关。此外,OPC 的形态分析显示 rhEPO 处理动物的突起长度减少。rhEPO 处理可增加体外 CSPG 暴露后 OPC 的增殖。使用 siRNA 进行红细胞生成素受体 (EPOr) 基因敲低可防止 rhEPO 诱导的 OPC 增殖,表明 rhEPO 对 OPC 反应的影响依赖于 EPOr 激活。总之,我们的研究结果表明,rhEPO 给药可能通过增加 TBI 后少突胶质谱系细胞的增殖来促进髓鞘形成。