Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3057374 | Experimental Neurology | 2006 | 4 Pages |
Abstract
Multipotential bone marrow stromal cells (MSCs) from wild-type (Wt) or apolipoprotein E deficient (Apoeâ/â) mice were implanted into the cerebral ventricles of Apoeâ/â mice. MSCs from Wt mice continued expressing apoE up to 6Â months after implantation and were associated with enhanced novel object recognition and increased microtubule-associated protein 2 (MAP2) immunoreactivity in the dentate gyrus. These data show that MSCs can be used to distinguish developmental from post-developmental effects of a gene knockout and support their therapeutic potential for neurodegenerative diseases.
Related Topics
Life Sciences
Neuroscience
Neurology
Authors
Alexandra Peister, Suzanne Zeitouni, Timothy Pfankuch, Roxanne L. Reger, Darwin J. Prockop, Jacob Raber,