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Regulation of the Ras cycle in neutrophils

Reference	BBS/E/B/0000L172
Principal Investigator / Supervisor	Professor Len Stephens
Co-Investigators / Co-Supervisors
Institution	Babraham Institute
Department	Babraham Institute Department
Funding type	Research
Value (£)	126,974
Status	Completed
Type	Institute Project
Start date	01/02/2006
End date	31/01/2009
Duration	36 months

Abstract

White blood cells called neutrophils play an important role within the immune system fighting infections. They are able to migrate towards sites of infection and destroy germs. We have proven, using genetically modified mice, that a special class of small GTPase protein, found inside neutrophils is essential for the processes of migration and destruction. At the moment it is not known how these proteins are controlled in neutrophils. Establishing the mechanism is an important part of the bigger process of attempting to understand migration and germ-killing and hence more clearly appreciate what goes wrong with these processes in a number of diseases such as arthritis and familial weakness to infection.The attractants, that drive migration, and the germs initiate the processes of killing and migration by binding to specialised molecules found on the cell surface, called receptors. Once activated the receptors stimulate further signalling through networks of molecules inside cells, to the machinery that causes migration, found at the front and back of the cell, and germ-killing, found inside the cell.We hypothesise that small GTPase proteins play an important role in focusing the signals down to the correct location in the cell where the relevant cell machinery is found.At the moment it is not clear how they are activated in neutrophils, neither in terms of the identity of the molecules responsible or the mechanism.We plan to use an approach that enables us to create mice specifically lacking signalling proteins in their white blood cells and then to test whether the white blood cells from those mice work normally. Once we have identifed the key molecules that regulate small GTPase, then it is possible in the future for drug or Biotech companies to test the possibility that they might represent good targets for drugs designed to treat diseases like arthritis.

Summary

unavailable

Committee	Closed Committee - Biochemistry & Cell Biology (BCB)
Research Topics	Immunology, Stem Cells
Research Priority	X – Research Priority information not available
Research Initiative	X - not in an Initiative
Funding Scheme	X – not Funded via a specific Funding Scheme

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