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BBSRC David Phillips Fellowship Mechanisms of TNF action in obesity and insulin resistance

ReferenceJF16994
Principal Investigator / Supervisor Professor Jaswinder Sethi
Co-Investigators /
Co-Supervisors
Institution University of Cambridge
DepartmentClinical Biochemistry
Funding typeResearch
Value (£) 385,784
StatusCompleted
TypeFellowships
Start date 01/01/2002
End date 31/12/2006
Duration60 months

Abstract

The specific questions to be addressed in this research programme are; 1). Is TNF alpha utilising the common TRAF2-mediated JNK/p38 activation to modify IRS-1 phosphorylation? 2). What are the intracellular domains of each TNFR that are absolutely required to mediate TNF alpha induced serine phosphorylation of IRS-1? 3). Is JNK and/or p38 activity increased in tissues from obese and type 2 DM subjects and rodents and does this correlate with increased serine phosphorylation of IRS-1? 4). Does TNF alpha-induced modification of IRS phosphorylation impinge on IGFR-TK in a fashion that is analogous to IR signalling?

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 Fellowship - David Phillips Fellowship (DF) [1995-2015]
Funding SchemeX – not Funded via a specific Funding Scheme
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