EXCEED THE SPACE PROVIDED. Axonal regenerationhas nowbeen demonstratedto occurin regionsof the CNS where it was formerly thoughtto be impossible. These dramaticexamplesof successfulregrowthhavecome from studiesin whichthe influenceof bothinhibitorsand promotersof neuritegrowthhave been examined. The importance of neuronalgrowthstate on regenerationsuccesshas recentlybeen demonstratedinstudiesof opticnerve regeneration. Collectively,these resultspointto the importanceof factorsthat normallystimulategrowthin overcomingthe non-permissivefeatures of CNS whitematter. The work proposedhere willtake advantage of techniquesthat have been developedinthis laboratoryover severalyears that permitassessmentof the role of NGF in stimulatingaxonalgrowthwithinthe CNS. Transgenicmice inwhich NGF is overexpressed underthe controlof an astrocyte-specificpromoter(GFAP), will be usedfor bothinvitroand invivo studies of axonalgrowth inCNS white matter. Invivostudiesof sympatheticaxonalgrowthwithinCNS regionsof such mice willbe carried outto determinethe extentto whichectopicexpressionof NGF modifiesthe growth of these aberrant fibers. In addition,tissuesectionculturestudieswillbe carriedoutto determinewhether NGF, either appliedexogenouslyor expressedtransgenically,willmodifythe generallynon-permissive natureof CNS white matterin supportingaxonalgrowth. Finally,the role of p75, the low-affinityNGF receptor,inmodifyingaxonalgrowthof NGF-responsiveneuronsinCNS white matterwillbe studiedthrough a seriesof transplantand tissuecultureapproachesusingtransgenicmiceinwhich p75 is deficientinthe presenceof NGF overexpression.The primarygoalis to studythe roleof neurotrophicfactorsin stimulating axonalregenerationwithinCNS white matter. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS044972-03
Application #
6825707
Study Section
Special Emphasis Panel (ZRG1-BDCN-2 (01))
Program Officer
Mamounas, Laura
Project Start
2002-12-01
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2005-11-30
Support Year
3
Fiscal Year
2005
Total Cost
$291,650
Indirect Cost
Name
University of Cincinnati
Department
Neurosurgery
Type
Schools of Medicine
DUNS #
041064767
City
Cincinnati
State
OH
Country
United States
Zip Code
45221
Pettigrew, David B; Li, Ya-Qin; Kuntz 4th, Charles et al. (2007) Global expression of NGF promotes sympathetic axonal growth in CNS white matter but does not alter its parallel orientation. Exp Neurol 203:95-109
Dhanoa, Navnish K; Krol, Karmen M; Jahed, Ali et al. (2006) Null mutations for exon III and exon IV of the p75 neurotrophin receptor gene enhance sympathetic sprouting in response to elevated levels of nerve growth factor in transgenic mice. Exp Neurol 198:416-26
Bierl, Michael A; Jones, Elizabeth E; Crutcher, Keith A et al. (2005) 'Mature' nerve growth factor is a minor species in most peripheral tissues. Neurosci Lett 380:133-7