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- Publisher Website: 10.1038/ni.2478
- Scopus: eid_2-s2.0-84871212540
- PMID: 23179078
- WOS: WOS:000312433800007
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Article: ARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system
Title | ARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system |
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Authors | |
Issue Date | 2013 |
Citation | Nature Immunology, 2013, v. 14, n. 1, p. 27-33 How to Cite? |
Abstract | The 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 Identifier | http://hdl.handle.net/10722/292030 |
ISSN | 2023 Impact Factor: 27.7 2023 SCImago Journal Rankings: 11.274 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lin, Amy E. | - |
dc.contributor.author | Ebert, Gregor | - |
dc.contributor.author | Ow, Yongkai | - |
dc.contributor.author | Preston, Simon P. | - |
dc.contributor.author | Toe, Jesse G. | - |
dc.contributor.author | Cooney, James P. | - |
dc.contributor.author | Scott, Hamish W. | - |
dc.contributor.author | Sasaki, Masato | - |
dc.contributor.author | Saibil, Samuel D. | - |
dc.contributor.author | Dissanayake, Dilan | - |
dc.contributor.author | Kim, Raymond H. | - |
dc.contributor.author | Wakeham, Andrew | - |
dc.contributor.author | You-Ten, Annick | - |
dc.contributor.author | Shahinian, Arda | - |
dc.contributor.author | Duncan, Gordon | - |
dc.contributor.author | Silvester, Jennifer | - |
dc.contributor.author | Ohashi, Pamela S. | - |
dc.contributor.author | Mak, Tak W. | - |
dc.contributor.author | Pellegrini, Marc | - |
dc.date.accessioned | 2020-11-17T14:55:37Z | - |
dc.date.available | 2020-11-17T14:55:37Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Nature Immunology, 2013, v. 14, n. 1, p. 27-33 | - |
dc.identifier.issn | 1529-2908 | - |
dc.identifier.uri | http://hdl.handle.net/10722/292030 | - |
dc.description.abstract | The 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.language | eng | - |
dc.relation.ispartof | Nature Immunology | - |
dc.title | ARIH2 is essential for embryogenesis, and its hematopoietic deficiency causes lethal activation of the immune system | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1038/ni.2478 | - |
dc.identifier.pmid | 23179078 | - |
dc.identifier.scopus | eid_2-s2.0-84871212540 | - |
dc.identifier.volume | 14 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 27 | - |
dc.identifier.epage | 33 | - |
dc.identifier.eissn | 1529-2916 | - |
dc.identifier.isi | WOS:000312433800007 | - |
dc.identifier.issnl | 1529-2908 | - |