Award details

Molecular mechanisms of B Lymphocyte differentiation and activation

ReferenceBBS/E/B/0000M206
Principal Investigator / Supervisor Dr Martin Turner
Co-Investigators /
Co-Supervisors
Institution Babraham Institute
DepartmentBabraham Institute Department
Funding typeResearch
Value (£) 256,306
StatusCompleted
TypeInstitute Project
Start date 01/07/2007
End date 30/06/2011
Duration48 months

Abstract

The B cell is a crucial component of the normal immune system, however its dysregulation can lead to certain types of leukaemia, lymphoma and myeloma. Further understanding of the molecular regulation of B cell differentiation (specialisation) is important for progress in vaccine design and for the development of therapies to treat autoimmunity and B cell malignancies. The importance of a regulatory network of transcription factors (proteins which bind to DNA to transfer information into RNA) controlling B cell identity and differentiation is well established. However, important mechanistic gaps in our knowledge remain. In particular, the relative role of post-transcriptional (post-RNA production) control in the regulation of B cell differentiation remains unclear. We have limited knowledge of the signalling mechanisms that drive naive B cells to become germinal centre (GC) B cells and the signals that promote differentiation of GC B cells into the alternative cell fates of memory versus plasma cells. Post-transcriptional control could impart both speed and sensitivity to these processes. This project seeks to understand how B cell differentiation is regulated and to understand the importance of post-transcriptional control in that process.

Summary

unavailable
Committee Closed Committee - Biochemistry & Cell Biology (BCB)
Research TopicsImmunology
Research PriorityX – Research Priority information not available
Research Initiative X - not in an Initiative
Funding SchemeX – not Funded via a specific Funding Scheme
terms and conditions of use (opens in new window)
export PDF file