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Grafting Neural Stem and Progenitor Cells Into the Hippocampus of Juvenile, Irradiated Mice Normalizes Behavior Deficits

Artikel i vetenskaplig tidskrift
Författare Yoshiaki Sato
Noriko Shinjyo
Machiko Sato
Marie Nilsson
Kazuhiro Osato
Changlian Zhu
Marcela Pekna
Hans-Georg Kuhn
Klas Blomgren
Publicerad i Frontiers in Neurology
Volym 9
ISSN 1664-2295
Publiceringsår 2018
Publicerad vid Institutionen för neurovetenskap och fysiologi
Språk en
Länkar dx.doi.org/10.3389/fneur.2018.00715
Ämnesord neural stem progenitor cells, irradiation, transplantation, grafting, learning deficits, developing brain, young-mouse brain, population-based cohort, long-term, stem/progenitor, cells, cognitive performance, neurotrophic factors, ionizing-radiation, spinal-cord, neurogenesis, adult, Neurosciences & Neurology, wler jf, 1989, british journal of radiology, v62, p679, ates of america, v114, pe820, ates of america, v105, p14632, ates of america, v106, p19150
Ämneskategorier Neurovetenskaper

Sammanfattning

The pool of neural stem and progenitor cells (NSPCs) in the dentate gyrus of the hippocampus is reduced by ionizing radiation. This explains, at least partly, the learning deficits observed in patients after radiotherapy, particularly in pediatric cases. An 8 Gy single irradiation dose was delivered to the whole brains of postnatal day 9 (P9) C57BL/6 mice, and BrdU-labeled, syngeneic NSPCs (1.0 x 10(5 )cells/injection) were grafted into each hippocampus on P21. Three months later, behavior tests were performed. Irradiation impaired novelty-induced exploration, place learning, reversal learning, and sugar preference, and it altered the movement pattern. Grafting of NSPCs ameliorated or even normalized the observed deficits. Less than 4% of grafted cells survived and were found in the dentate gyrus 5 months later. The irradiation-induced loss of endogenous, undifferentiated NSPCs in the dentate gyrus was completely restored by grafted NSPCs in the dorsal, but not the ventral, blade. The grafted NSPCs did not exert appreciable effects on the endogenous NSPCs; however, more than half of the grafted NSPCs differentiated. These results point to novel strategies aimed at ameliorating the debilitating late effects of cranial radiotherapy, particularly in children.

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