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DOI 10.3233/rnn-140404

Медицинская библиотека · Restorative neurology and neuroscience · 2014

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

Tatarishvili Jemal, Oki Koichi, Monni Emanuela, Koch Philipp, Memanishvili Tamar, Buga Ana-Maria, Verma Vivek, Popa-Wagner Aurel, Brüstle Oliver, Lindvall Olle, Kokaia Zaal

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Tatarishvili Jemal, Oki Koichi, Monni Emanuela, Koch Philipp, Memanishvili Tamar, Buga Ana-Maria, Verma Vivek, Popa-Wagner Aurel, Brüstle Oliver, Lindvall Olle, Kokaia Zaal. Human induced pluripotent stem cells improve recovery in stroke-injured aged rats.. Restorative neurology and neuroscience. 2014. DOI: 10.3233/rnn-140404.

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