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Investigating the mechanism by which tissue inhibitor of metalloproteinase-1 (TIMP-1) is neuroprotective

ReferenceC18365
Principal Investigator / Supervisor Professor James Uney
Co-Investigators /
Co-Supervisors
Professor Jeremy Henley
Institution University of Bristol
DepartmentPhysiology and Pharmacology
Funding typeResearch
Value (£) 170,388
StatusCompleted
TypeResearch Grant
Start date 01/04/2003
End date 30/09/2006
Duration42 months

Abstract

Results obtained in a previous study have lead us to hypothesise that TIMP-1 may protect neurons from excitotoxic damage by inhibiting glutamate mediated calcium influx into neurones. The main aims of this study are: to investigate whether: (i) TIMP-1 is inhibiting calcium influx via an effect on the trafficking and or function of NMDA or AMPA and Kainate receptors; (ii) use TIMP-1 mutants to confirm that TIMP-1 mediates neuroprotective effects independently of its actions on matrix metalloproteinases (MMPs); (iii) examine the significance of interactions between TIMP-1 and known cellular proteins identified by yeast two-hybrid analysis.

Summary

unavailable
Committee Closed Committee - Biochemistry & Cell Biology (BCB)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
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