File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: ARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system

TitleARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system
Authors
Issue Date2013
Citation
Nature Immunology, 2013, v. 14, n. 1, p. 27-33 How to Cite?
AbstractThe E3 ligase ARIH2 has an unusual structure and mechanism of elongating ubiquitin chains. To understand its physiological role, we generated gene-targeted mice deficient in ARIH2. ARIH2 deficiency resulted in the embryonic death of C57BL/6 mice. On a mixed genetic background, the lethality was attenuated, with some mice surviving beyond weaning and then succumbing to an aggressive multiorgan inflammatory response. We found that in dendritic cells (DCs), ARIH2 caused degradation of the inhibitor IκBβ in the nucleus, which abrogated its ability to sequester, protect and transcriptionally coactivate the transcription factor subunit p65 in the nucleus. Loss of ARIH2 caused dysregulated activation of the transcription factor NF-κB in DCs, which led to lethal activation of the immune system in ARIH2-sufficent mice reconstituted with ARIH2-deficient hematopoietic stem cells. Our data have therapeutic implications for targeting ARIH2 function. © 2013 Nature America, Inc. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/292030
ISSN
2022 Impact Factor: 30.5
2020 SCImago Journal Rankings: 9.074
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLin, Amy E.-
dc.contributor.authorEbert, Gregor-
dc.contributor.authorOw, Yongkai-
dc.contributor.authorPreston, Simon P.-
dc.contributor.authorToe, Jesse G.-
dc.contributor.authorCooney, James P.-
dc.contributor.authorScott, Hamish W.-
dc.contributor.authorSasaki, Masato-
dc.contributor.authorSaibil, Samuel D.-
dc.contributor.authorDissanayake, Dilan-
dc.contributor.authorKim, Raymond H.-
dc.contributor.authorWakeham, Andrew-
dc.contributor.authorYou-Ten, Annick-
dc.contributor.authorShahinian, Arda-
dc.contributor.authorDuncan, Gordon-
dc.contributor.authorSilvester, Jennifer-
dc.contributor.authorOhashi, Pamela S.-
dc.contributor.authorMak, Tak W.-
dc.contributor.authorPellegrini, Marc-
dc.date.accessioned2020-11-17T14:55:37Z-
dc.date.available2020-11-17T14:55:37Z-
dc.date.issued2013-
dc.identifier.citationNature Immunology, 2013, v. 14, n. 1, p. 27-33-
dc.identifier.issn1529-2908-
dc.identifier.urihttp://hdl.handle.net/10722/292030-
dc.description.abstractThe E3 ligase ARIH2 has an unusual structure and mechanism of elongating ubiquitin chains. To understand its physiological role, we generated gene-targeted mice deficient in ARIH2. ARIH2 deficiency resulted in the embryonic death of C57BL/6 mice. On a mixed genetic background, the lethality was attenuated, with some mice surviving beyond weaning and then succumbing to an aggressive multiorgan inflammatory response. We found that in dendritic cells (DCs), ARIH2 caused degradation of the inhibitor IκBβ in the nucleus, which abrogated its ability to sequester, protect and transcriptionally coactivate the transcription factor subunit p65 in the nucleus. Loss of ARIH2 caused dysregulated activation of the transcription factor NF-κB in DCs, which led to lethal activation of the immune system in ARIH2-sufficent mice reconstituted with ARIH2-deficient hematopoietic stem cells. Our data have therapeutic implications for targeting ARIH2 function. © 2013 Nature America, Inc. All rights reserved.-
dc.languageeng-
dc.relation.ispartofNature Immunology-
dc.titleARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1038/ni.2478-
dc.identifier.pmid23179078-
dc.identifier.scopuseid_2-s2.0-84871212540-
dc.identifier.volume14-
dc.identifier.issue1-
dc.identifier.spage27-
dc.identifier.epage33-
dc.identifier.eissn1529-2916-
dc.identifier.isiWOS:000312433800007-
dc.identifier.issnl1529-2908-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats