Physiol. Genomics Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics 14: 171-197, 2003; doi:10.1152/physiolgenomics.00021.2002
1094-8341/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Imitola, J.
Right arrow Articles by Khoury, S. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Imitola, J.
Right arrow Articles by Khoury, S. J.
Physiological Genomics 14:171-197 (2003)
1094-8341/03 $5.00 © 2003 American Physiological Society

Invited Review

Genetic programs and responses of neural stem/progenitor cells during demyelination: potential insights into repair mechanisms in multiple sclerosis

Jaime Imitola1, Evan Y. Snyder2 and Samia J. Khoury1

1 Center for Neurologic Diseases, Partners MS Center, Department of Neurology, Brigham and Women’s Hospital
2 Department of Neurology, Harvard Institutes of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston Massachusetts 02115

In recent years, it has become evident that the adult mammalian CNS contains a population of neural stem cells (NSCs) described as immature, undifferentiated, multipotent cells, that may be called upon for repair in neurodegenerative and demyelinating diseases. NSCs may give rise to oligodendrocyte progenitor cells (OPCs) and other myelinating cells. This article reviews recent progress in elucidating the genetic programs and dynamics of NSC and OPC proliferation, differentiation, and apoptosis, including the response to demyelination. Emerging knowledge of the molecules that may be involved in such responses may help in the design of future stem cell-based treatment of demyelinating diseases such as multiple sclerosis.

neural stem cells; experimental autoimmune encephalomyelitis; neuroregeneration; cytokines; neural transplantation; neurodegeneration




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
T.-Y. Eom, K. A. Roth, and R. S. Jope
Neural Precursor Cells Are Protected from Apoptosis Induced by Trophic Factor Withdrawal or Genotoxic Stress by Inhibitors of Glycogen Synthase Kinase 3
J. Biol. Chem., August 3, 2007; 282(31): 22856 - 22864.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
J. Imitola, T. Chitnis, and S. J. Khoury
Insights Into the Molecular Pathogenesis of Progression in Multiple Sclerosis: Potential Implications for Future Therapies
Arch Neurol, January 1, 2006; 63(1): 25 - 33.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Imitola, K. Raddassi, K. I. Park, F.-J. Mueller, M. Nieto, Y. D. Teng, D. Frenkel, J. Li, R. L. Sidman, C. A. Walsh, et al.
Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1{alpha}/CXC chemokine receptor 4 pathway
PNAS, December 28, 2004; 101(52): 18117 - 18122.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
J. Imitola, M. Comabella, A. K. Chandraker, F. Dangond, M. H. Sayegh, E. Y. Snyder, and S. J. Khoury
Neural Stem/Progenitor Cells Express Costimulatory Molecules That Are Differentially Regulated by Inflammatory and Apoptotic Stimuli
Am. J. Pathol., May 1, 2004; 164(5): 1615 - 1625.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2003 by the American Physiological Society.