Ph.D. Program for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University and National Health Research Institutes, Taipei, Taiwan.
TMU Neuroscience Research Center, Taipei Medical University, Taipei, Taiwan.
J Neurotrauma. 2020 Jan 1;37(1):14-26. doi: 10.1089/neu.2019.6422. Epub 2019 Aug 20.
Traumatic brain injury (TBI) is a progressive and complex pathological condition that results in multiple adverse consequences, including impaired learning and memory. Transplantation of mesenchymal stem cells (MSCs) has produced limited benefits in experimental TBI models. Fibroblast growth factor 21 (FGF21) is a novel metabolic regulator that has neuroprotective effects, promotes remyelination, enhances angiogenesis, and elongates astrocytic processes. In this study, MSCs were genetically engineered to overexpress FGF21 in order to improve their efficacy in TBI. MSCs overexpressing FGF21 (MSC-FGF21) were transplanted to mouse brain by intracerebroventricular injection 24 h after TBI was induced by controlled cortical impact (CCI). Hippocampus-dependent spatial learning and memory, assessed by the Morris water maze test, was markedly decreased 3-4 weeks after TBI, a deficit that was robustly recovered by treatment with MSC-FGF21, but not MSC-mCherry control. Hippocampus-independent learning and memory, assessed by the novel object recognition test, was also impaired; these effects were blocked by treatment with both MSC-FGF21 and MSC-mCherry control. FGF21 protein levels in the ipsilateral hippocampus were drastically reduced 4 weeks post-TBI, a loss that was restored by treatment with MSC-FGF21, but not MSC-mCherry. MSC-FGF21 treatment also partially restored TBI-induced deficits in neurogenesis and maturation of immature hippocampal neurons, whereas MSC-mCherry was less effective. Finally, MSC-FGF21 treatment also normalized TBI-induced impairments in dendritic arborization of hippocampal neurons. Taken together, the results indicate that MSC-FGF21 treatment significantly improved TBI-induced spatial memory deficits, impaired hippocampal neurogenesis, and abnormal dendritic morphology. Future clinical investigations using MSC-FGF21 to improve post-TBI outcomes are warranted.
创伤性脑损伤 (TBI) 是一种进行性且复杂的病理状况,会导致多种不良后果,包括学习和记忆受损。间充质干细胞 (MSCs) 的移植在实验性 TBI 模型中产生的益处有限。成纤维细胞生长因子 21 (FGF21) 是一种新型代谢调节剂,具有神经保护作用,促进髓鞘再生,增强血管生成,并延长星形胶质细胞的突起。在这项研究中,通过基因工程使 MSCs 过表达 FGF21,以提高其在 TBI 中的疗效。在 TBI 由皮质冲击控制 (CCI) 诱导 24 小时后,通过侧脑室注射将过表达 FGF21 的 MSCs (MSC-FGF21) 移植到小鼠大脑中。Morris 水迷宫测试评估海马依赖性空间学习和记忆,TBI 后 3-4 周明显下降,MSC-FGF21 治疗可显著恢复这种缺陷,但 MSC-mCherry 对照则不能。新物体识别测试评估的海马不依赖学习和记忆也受到损害;MSC-FGF21 和 MSC-mCherry 对照的治疗均阻断了这些影响。TBI 后 4 周,对侧海马中的 FGF21 蛋白水平急剧下降,MSC-FGF21 治疗可恢复这种下降,但 MSC-mCherry 则不能。MSC-FGF21 治疗还部分恢复了 TBI 诱导的神经发生和不成熟海马神经元成熟的缺陷,而 MSC-mCherry 则效果较差。最后,MSC-FGF21 治疗还可使 TBI 诱导的海马神经元树突分支异常正常化。总之,这些结果表明,MSC-FGF21 治疗可显著改善 TBI 诱导的空间记忆缺陷、海马神经发生受损和异常树突形态。未来使用 MSC-FGF21 改善 TBI 后结局的临床研究是必要的。