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Analysis of handling of apoptotic cells by DCs derived from normal and autoimmune prone mice

ReferenceBBS/B/0370X
Principal Investigator / Supervisor Professor Anne Cooke
Co-Investigators /
Co-Supervisors
Dr Tina Rich
Institution University of Cambridge
DepartmentPathology
Funding typeResearch
Value (£) 187,935
StatusCompleted
TypeResearch Grant
Start date 12/07/2004
End date 11/07/2007
Duration36 months

Abstract

Cells can die by necrosis or apoptosis. While the former mode of death can lead to inflammation the latter is thought to be tolerated by the immune system. It has been suggested that defective clearance of apoptotic bodies breaks this tolerance. This hypothesis can be tested using cells that are predestined to drive an inflammatory response. We have designed a series of experiments to investigate how the normal and inflammatory response to apoptotic cells develops, in terms of defects in both the effector and target cells. These data can be applied to all fundamental processes that rely on apoptotic clearance to maintain normal cellular homeoastasis. As such they are relevant to basic developmental disorders, autoimmunity, persistent viral infection and neurodegeneration.

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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