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Requirement of Hsp90 activity for IkappaB kinase (IKK) biosynthesis and for constitutive and inducible IKK and NF-kappaB activation

Item Type:Article
Title:Requirement of Hsp90 activity for IkappaB kinase (IKK) biosynthesis and for constitutive and inducible IKK and NF-kappaB activation
Creators Name:Broemer, M. and Krappmann, D. and Scheidereit, C.
Abstract:The molecular chaperone Hsp90 affects the function and fate of a number of signaling molecules. We have investigated the Hsp90 requirement for constitutive and inducible activity of the IκB kinase (IKK) complex and of NF-κB. Inhibition by the Hsp90 ATPase inhibitors, geldanamycin (GA) and radicicol (RC), revealed that Hsp90 controls IKKs at two levels, inducibility of enzymatic activity and biogenesis, which can be discriminated by short- and long-time GA incubation, respectively. Short-time inhibition of Hsp90 resulted in impaired IKK kinase activation by TNF{alpha}, IL-1{beta} or phorbolester PMA. Furthermore, GA inhibited constitutive activation of IKK and NF-κB in Hodgkin's lymphoma cells. Hsp90 function was also required for trans- and autophosphorylation of transfected IKKβ. GA exposure for several hours resulted in a downmodulation of IKK complex {alpha}, {beta} and {gamma} subunits to various extent. Proteasome inhibition interfered with GA mediated IKK depletion and Hsp90 inhibition induced polyubiquitination of IKK{alpha} and {beta} during protein synthesis. In fact, GA blocked biogenesis of IKKα and IKKβ but did not interfere with post-translational turnover. Together, these results define a dual requirement for Hsp90 as a regulator of NF-κB signaling by its general involvement in IKK activation and by its role in IKK homeostasis.
Keywords:Chaperones, Proteasome, Reed-Sternberg Cells, Ribosome, Tumor cell Pharmacology, Ubiquitin, Animals
Source:Oncogene
ISSN:0950-9232
Publisher:Nature Publishing Group (U.K.)
Volume:23
Number:31
Page Range:5378-5386
Date:8 July 2004
Official Publication:https://doi.org/10.1038/sj.onc.1207705
PubMed:View item in PubMed

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