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Molecular mechanisms controlling angiogenic signalling from the sphingosine-1 phosphate receptors edg1 and edg3

ReferenceC14576
Principal Investigator / Supervisor Professor Timothy Palmer
Co-Investigators /
Co-Supervisors
Institution University of Glasgow
DepartmentIBLS Division of Biochemistry & Molecula
Funding typeResearch
Value (£) 194,120
StatusCompleted
TypeResearch Grant
Start date 17/04/2001
End date 16/04/2004
Duration36 months

Abstract

Diabetic retinopathy, rheumatoid arthritis and cancer are each associated with excessive angiogenesis, defined as the formation of new capillaries from pre-existing blood vessels. Inhibiting angiogenesis in these diseases will require a detailed molecular understanding of the regulatory factors that direct the maturation of endothelial cells into mature blood vessels. One such factor is the bioactive lipid sphingosine-1-phosphate (SSP), which promotes angiogenesis by binding to two endothelial cell surface SPP receptors termed EDG1 and EDG3. This application aims to identify the cellular and molecular mechanisms by which distinct EDG1- and EDG3-activated signalling pathways are regulated in human endothelial cells.

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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