Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340731
Title: The role of the p38 MAP kinase substrate, MAPKAPK-2 in proinflammatory cytokine signalling
Author: Lumb, Simon
ISNI:       0000 0001 3613 9432
Awarding Body: Open University
Current Institution: Open University
Date of Award: 2001
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Abstract:
The pro-inflammatory cytokine IL-1 induces the synthesis of many genes during inflammation. The signalling mechanisms triggered by IL-1 include activation of several distinct parallel MAP kinase pathways. The p38 MAP kinase pathway is activated particularly strongly by this cytokine. MAPKAP kinase-2 (MAPKAPK-2) is one of several p38 substrates that are regulated by direct phosphorylation. Few MAPKAPK-2 substrates are known. One of these, the small heat shock protein 27 (Hsp27), is rapidly phosphorylated following MAPKAPK-2 activation. In an attempt to delineate the role of MAPKAPK-2 in IL-1 signalling, IL-1 a induced MAPKAPK-2 activity was inhibited by stable overexpression of dominant negative (MAPKAPK-2 K93R) and MAPKAPK-2 anti-sense RNA (MAPKAPK-2 A/S) in HeLa cells. IL-1 a strongly induced COX-2 protein in empty vector transfected cells. In contrast MAPKAPK-2 K93R and MAPKAPK-2 A/S overexpressing cells strongly inhibited COX-2 protein and mRNA In addition IL-la induced IL-6 synthesis was also strongly inhibited by MAPKAPK-2 A/S. These results suggest that MAPKAPK-2 may act as an effector molecule involved in IL-la induced COX-2 and IL-6 synthesis. In an attempt to identify new MAPKAPK-2 substrates, yeast two-hybrid screening of a human leukocyte cDNA library identified a novel protein interaction between MAPKAPK-2 K93R and a close homologue of the human polyhomeotic 2 (HPH2) protein.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.340731  DOI:
Keywords: Immunology; Tumour necrosis
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