Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.625350
Title: Role of the Syk tyrosine kinase in mature B cell function
Author: Nys, J.
Awarding Body: University College London (University of London)
Current Institution: University College London (University of London)
Date of Award: 2010
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Abstract:
Signal transduction through the antigen receptor of B cells (BCR) is crucial in controlling their development and maintenance, and is also needed for B cell immune responses. Syk, a protein tyrosine kinase, has already been implicated in signalling downstream of the BCR. Mice deficient for Syk show a developmental block at the immature to mature B cell stage such that no mature B cells are generated. Thus it has not been possible to use these targeted mice to study the role of Syk in the activation of mature B cells or in antigen-driven B cell responses. To get around this, I used mice with an inducible conditional knock out (CoKO) of Syk to generate mature B cells lacking Syk. This has allowed me to study the role of Syk in mature B cell activation and its involvement in the immune response. In this work I show that B cells from Syk CoKO mice are unable to respond to BCR stimulation. I also addressed the requirement in Syk for T-dependent immune responses, looking at both primary and secondary responses. The primary response was Syk-dependent, while, surprisingly, the secondary response seems to be Syk-independent. Finally, I investigated the role of Syk downstream of TLR receptors. Unexpectedly, Syk CoKO B cells were unresponsive to TLR4 stimulation. This defect is B cell autonomous and may be due to reduced signaling through the Akt/Gsk-3/cMyc pathway, downstream of the BCR.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.625350  DOI: Not available
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