Lee Eun Ji, Lee Min-Ju, Ryu Ye Jin, Nam Sang-Hyeon, Kim Rokhyun, Song Sehyeon, Park Kyunghyuk, Park Young Jun, Kim Jong-Il, Koh Seong-Ho, Chang Mi-Sook
Department of Translational Medical Science, Hanyang University Graduate School of Biomedical Science & Engineering, Seoul 04763, Republic of Korea.
Laboratory of Stem Cell & Neurobiology, Department of Oral Anatomy and Dental Research Institute, Seoul National University School of Dentistry, Seoul 03080, Republic of Korea.
Mol Ther. 2025 Jan 8;33(1):356-374. doi: 10.1016/j.ymthe.2024.11.022. Epub 2024 Nov 19.
Despite a dramatic increase in ischemic stroke incidence worldwide, effective therapies for attenuating sequelae of cerebral infarction are lacking. This study investigates the use of human mesenchymal stem cells (hMSCs) induced toward glia-like cells (ghMSCs) to ameliorate chronic sequelae resulting from cerebral infarction. Transcriptome analysis demonstrated that ghMSCs exhibited astrocytic characteristics, and assessments conducted ex vivo using organotypic brain slice cultures demonstrated that ghMSCs exhibited superior neuroregenerative and neuroprotective activity against ischemic damage compared to hMSCs. The observed beneficial effects of ghMSCs were diminished by pre-treatment with a CXCR2 antagonist, indicating a direct role for CXCR2 signaling. Studies conducted in rats subjected to cerebral infarction demonstrated that ghMSCs restored neurobehavioral functions and reduced chronic brain infarction in a dose-dependent manner when transplanted at the subacute-to-chronic phase. These beneficial impacts were also inhibited by a CXCR2 antagonist. Molecular analyses confirmed that increased neuroplasticity contributed to ghMSCs' neuroregenerative effects. These data indicate that ghMSCs hold promise for treating refractory sequelae resulting from cerebral infarction by enhancing neuroplasticity and identify CXCR2 signaling as an important mediator of ghMSCs' mechanism of action.
尽管全球缺血性中风的发病率急剧上升,但目前仍缺乏有效减轻脑梗死后遗症的治疗方法。本研究探讨了诱导分化为神经胶质样细胞(ghMSCs)的人间充质干细胞(hMSCs)用于改善脑梗死所致慢性后遗症的效果。转录组分析表明,ghMSCs表现出星形胶质细胞的特征,使用脑片器官型培养物进行的体外评估表明,与hMSCs相比,ghMSCs对缺血性损伤表现出更强的神经再生和神经保护活性。用CXCR2拮抗剂预处理可减弱ghMSCs观察到的有益作用,表明CXCR2信号传导起直接作用。在脑梗死大鼠中进行的研究表明,在亚急性至慢性期移植时,ghMSCs以剂量依赖的方式恢复神经行为功能并减少慢性脑梗死。这些有益影响也被CXCR2拮抗剂抑制。分子分析证实,神经可塑性增加有助于ghMSCs的神经再生作用。这些数据表明,ghMSCs有望通过增强神经可塑性来治疗脑梗死引起的难治性后遗症,并确定CXCR2信号传导是ghMSCs作用机制的重要介质。