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Implantation Site and Lesion Topology Determine Efficacy of a Human Neural Stem Cell Line in a Rat Model of Chronic Stroke

Authors :
E Tang
Edward J. Smith
John Sinden
Lara Stevanato
R. Paul Stroemer
William R. Crum
Mitsuko Nakajima
Michel Modo
Natalia Gorenkova
Source :
Stem Cells. 30:785-796
Publication Year :
2012
Publisher :
Oxford University Press (OUP), 2012.

Abstract

Stroke remains one of the most promising targets for cell therapy. Thorough preclinical efficacy testing of human neural stem cell (hNSC) lines in a rat model of stroke (transient middle cerebral artery occlusion) is, however, required for translation into a clinical setting. Magnetic resonance imaging (MRI) here confirmed stroke damage and allowed the targeted injection of 450,000 hNSCs (CTX0E03) into peri-infarct tissue, rather than the lesion cyst. Intraparenchymal cell implants improved sensorimotor dysfunctions (bilateral asymmetry test) and motor deficits (footfault test and rotameter). Importantly, analyses based on lesion topology (striatal vs. striatal + cortical damage) revealed a more significant improvement in animals with a stroke confined to the striatum. However, no improvement in learning and memory (water maze) was evident. An intracerebroventricular injection of cells did not result in any improvement. MRI-based lesion, striatal and cortical volumes were unchanged in treated animals compared to those with stroke that received an intraparenchymal injection of suspension vehicle. Grafted cells only survived after intraparenchymal injection with a striatal + cortical topology resulting in better graft survival (16,026 cells) than in animals with smaller striatal lesions (2,374 cells). Almost 20% of cells differentiated into glial fibrillary acidic protein+ astrocytes, but Disclosure of potential conflicts of interest is found at the end of this article.

Details

ISSN :
15494918 and 10665099
Volume :
30
Database :
OpenAIRE
Journal :
Stem Cells
Accession number :
edsair.doi.dedup.....95d4aed676700df1b2d67ff30c0491b3
Full Text :
https://doi.org/10.1002/stem.1024