Human induced pluripotent stem cells improve recovery in stroke-injured aged rats

被引:64
作者
Tatarishvili, Jemal [1 ]
Oki, Koichi [1 ]
Monni, Emanuela [1 ]
Koch, Philipp [2 ]
Memanishvili, Tamar [1 ,3 ]
Buga, Ana-Maria [4 ]
Verma, Vivek [1 ]
Popa-Wagner, Aurel [4 ]
Bruestle, Oliver [2 ]
Lindvall, Olle [1 ]
Kokaia, Zaal [1 ]
机构
[1] Univ Hosp, Lund Stem Cell Ctr, Lab Stem Cells & Restorat Neurol, SE-22184 Lund, Sweden
[2] Univ Bonn & Hertie Fundat, Life & Brain Ctr, Inst Reconstruct Neurobiol, Bonn, Germany
[3] I Javakhishvili Tbilisi State Univ, Tbilisi, Georgia
[4] Univ Rostock, Sch Med, Dept Psychiat & Mol Psychiat, D-18055 Rostock, Germany
基金
美国国家科学基金会; 瑞典研究理事会;
关键词
Stroke; neuroregeneration; inflammation; reprogramming; recovery; neural stem cell; aging; transplantation; CEREBRAL-ARTERY OCCLUSION; ISCHEMIC-STROKE; TOTAL NUMBER; NEURONS; MODEL; BRAIN; TRANSPLANTATION; ENHANCE; DIFFERENTIATE; DEGENERATION;
D O I
10.3233/RNN-140404
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Purpose: Induced pluripotent stem cells (iPSCs) improve behavior and form neurons after implantation into the stroke-injured adult rodent brain. How the aged brain responds to grafted iPSCs is unknown. We determined survival and differentiation of grafted human fibroblast-derived iPSCs and their ability to improve recovery in aged rats after stroke. Methods: Twenty-four months old rats were subjected to 30 min distal middle cerebral artery occlusion causing neocortical damage. After 48 h, animals were transplanted intracortically with human iPSC-derived long-term neuroepithelial-like stem (hiPSC-lt-NES) cells. Controls were subjected to stroke and were vehicle-injected. Results: Cell-grafted animals performed better than vehicle-injected recipients in cylinder test at 4 and 7 weeks. At 8 weeks, cell proliferation was low (0.7 %) and number of hiPSC-lt-NES cells corresponded to 49.2% of that of implanted cells. Transplanted cells expressed markers of neuroblasts and mature and GABAergic neurons. Cell-grafted rats exhibited less activated microglia/macrophages in injured cortex and neuronal loss was mitigated. Conclusions: Our study provides the first evidence that grafted human iPSCs survive, differentiate to neurons and ameliorate functional deficits in stroke-injured aged brain.
引用
收藏
页码:547 / 558
页数:12
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