HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.

The tumor necrosis factor receptor (TNFR) superfamily mediates signals critical for regulation of the immune system. One family member, CD40, is important for the efficient activation of antibody-producing B cells and other antigen-presenting cells. The molecules and mechanisms that mediate CD40 sig...

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Main Authors: Bruce S Hostager, Daniel K Fox, Douglas Whitten, Curtis G Wilkerson, Betty A Eipper, Victor P Francone, Paul B Rothman, John D Colgan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-06-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0011380&type=printable
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author Bruce S Hostager
Daniel K Fox
Douglas Whitten
Curtis G Wilkerson
Betty A Eipper
Victor P Francone
Paul B Rothman
John D Colgan
author_facet Bruce S Hostager
Daniel K Fox
Douglas Whitten
Curtis G Wilkerson
Betty A Eipper
Victor P Francone
Paul B Rothman
John D Colgan
author_sort Bruce S Hostager
collection DOAJ
description The tumor necrosis factor receptor (TNFR) superfamily mediates signals critical for regulation of the immune system. One family member, CD40, is important for the efficient activation of antibody-producing B cells and other antigen-presenting cells. The molecules and mechanisms that mediate CD40 signaling are only partially characterized. Proteins known to interact with the cytoplasmic domain of CD40 include members of the TNF receptor-associated factor (TRAF) family, which regulate signaling and serve as links to other signaling molecules. To identify additional proteins important for CD40 signaling, we used a combined stimulation/immunoprecipitation procedure to isolate CD40 signaling complexes from B cells and characterized the associated proteins by mass spectrometry. In addition to known CD40-interacting proteins, we detected SMAC/DIABLO, HTRA2/Omi, and HOIP/RNF31/PAUL/ZIBRA. We found that these previously unknown CD40-interacting partners were recruited in a TRAF2-dependent manner. HOIP is a ubiquitin ligase capable of mediating NF-kappaB activation through the ubiquitin-dependent activation of IKKgamma. We found that a mutant HOIP molecule engineered to lack ubiquitin ligase activity inhibited the CD40-mediated activation of NF-kappaB. Together, our results demonstrate a powerful approach for the identification of signaling molecules associated with cell surface receptors and indicate an important role for the ubiquitin ligase activity of HOIP in proximal CD40 signaling.
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spelling doaj-art-86d4cc668d754adb959614d8440bd1e62025-08-20T03:07:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-06-0156e1138010.1371/journal.pone.0011380HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.Bruce S HostagerDaniel K FoxDouglas WhittenCurtis G WilkersonBetty A EipperVictor P FranconePaul B RothmanJohn D ColganThe tumor necrosis factor receptor (TNFR) superfamily mediates signals critical for regulation of the immune system. One family member, CD40, is important for the efficient activation of antibody-producing B cells and other antigen-presenting cells. The molecules and mechanisms that mediate CD40 signaling are only partially characterized. Proteins known to interact with the cytoplasmic domain of CD40 include members of the TNF receptor-associated factor (TRAF) family, which regulate signaling and serve as links to other signaling molecules. To identify additional proteins important for CD40 signaling, we used a combined stimulation/immunoprecipitation procedure to isolate CD40 signaling complexes from B cells and characterized the associated proteins by mass spectrometry. In addition to known CD40-interacting proteins, we detected SMAC/DIABLO, HTRA2/Omi, and HOIP/RNF31/PAUL/ZIBRA. We found that these previously unknown CD40-interacting partners were recruited in a TRAF2-dependent manner. HOIP is a ubiquitin ligase capable of mediating NF-kappaB activation through the ubiquitin-dependent activation of IKKgamma. We found that a mutant HOIP molecule engineered to lack ubiquitin ligase activity inhibited the CD40-mediated activation of NF-kappaB. Together, our results demonstrate a powerful approach for the identification of signaling molecules associated with cell surface receptors and indicate an important role for the ubiquitin ligase activity of HOIP in proximal CD40 signaling.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0011380&type=printable
spellingShingle Bruce S Hostager
Daniel K Fox
Douglas Whitten
Curtis G Wilkerson
Betty A Eipper
Victor P Francone
Paul B Rothman
John D Colgan
HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
PLoS ONE
title HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
title_full HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
title_fullStr HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
title_full_unstemmed HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
title_short HOIL-1L interacting protein (HOIP) as an NF-kappaB regulating component of the CD40 signaling complex.
title_sort hoil 1l interacting protein hoip as an nf kappab regulating component of the cd40 signaling complex
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0011380&type=printable
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