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First published online June 28, 2007
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2007-0313v1
25/10/2396    most recent
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Submitted on April 26, 2007
Accepted on June 18, 2007

TISSUE-SPECIFIC STEM CELLS

Prospects of Stem Cell Therapy for Temporal Lobe Epilepsy

Ashok K. Shetty 1* and Bharathi Hattiangady 1

1 Department of Surgery (Neurosurgery), Duke University Medical Center, Durham NC 27710.; Medical Research and Surgery Services, Veterans Affairs Medical Center, Durham, North Carolina 27705.

* To whom correspondence should be addressed. E-mail: Ashok.Shetty{at}Duke.Edu.


   Abstract

Certain regions of the adult brain have the ability for partial self-repair after injury through production of new neurons via activation of neural stem/progenitor cells (NSCs). Nonetheless, there is no evidence yet for pervasive spontaneous replacement of dead neurons by newly formed neurons leading to functional recovery in the injured brain. Consequently, there is enormous interest for stimulating endogenous NSCs in the brain to produce new neurons or for grafting of NSCs isolated and expanded from different brain regions or embryonic stem cells into the injured brain. Temporal lobe epilepsy (TLE), characterized by hyperexcitability in the hippocampus and spontaneous seizures, is a possible clinical target for stem cell based therapies. This is because these approaches have the potential to curb epileptogenesis and prevent chronic epilepsy development and learning and memory dysfunction after hippocampal damage related to status epilepticus or head injury. Grafting of NSCs may also be useful for restraining seizures during chronic epilepsy. The aim of this review is to evaluate current knowledge and outlook pertaining to stem cell based therapies for TLE. The first section discusses the behavior of endogenous hippocampal NSCs in human TLE and animal models of TLE, and evaluates the role of hippocampal neurogenesis in the pathophysiology and treatment of TLE. The second segment considers the prospects for preventing or suppressing seizures in TLE using exogenously applied stem cells. The final part analyzes problems that remain to be resolved before initiating clinical application of stem cell based therapies for TLE.

Key Words. adult neurogenesis, dentate gyrus, epilepsy, hippocampal stem cells, hippocampal progenitors, neural stem cells, seizures, stem cell grafts







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