Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7196
pubmed:dateCreated
2008-6-5
pubmed:abstractText
The hypoxic response is an ancient stress response triggered by low ambient oxygen (O2) (ref. 1) and controlled by hypoxia-inducible transcription factor-1 (HIF-1), whose alpha subunit is rapidly degraded under normoxia but stabilized when O2-dependent prolyl hydroxylases (PHDs) that target its O2-dependent degradation domain are inhibited. Thus, the amount of HIF-1alpha, which controls genes involved in energy metabolism and angiogenesis, is regulated post-translationally. Another ancient stress response is the innate immune response, regulated by several transcription factors, among which NF-kappaB plays a central role. NF-kappaB activation is controlled by IkappaB kinases (IKK), mainly IKK-beta, needed for phosphorylation-induced degradation of IkappaB inhibitors in response to infection and inflammation. IKK-beta is modestly activated in hypoxic cell cultures when PHDs that attenuate its activation are inhibited. However, defining the relationship between NF-kappaB and HIF-1alpha has proven elusive. Using in vitro systems, it was reported that HIF-1alpha activates NF-kappaB, that NF-kappaB controls HIF-1alpha transcription and that HIF-1alpha activation may be concurrent with inhibition of NF-kappaB. Here we show, with the use of mice lacking IKK-beta in different cell types, that NF-kappaB is a critical transcriptional activator of HIF-1alpha and that basal NF-kappaB activity is required for HIF-1alpha protein accumulation under hypoxia in cultured cells and in the liver and brain of hypoxic animals. IKK-beta deficiency results in defective induction of HIF-1alpha target genes including vascular endothelial growth factor. IKK-beta is also essential for HIF-1alpha accumulation in macrophages experiencing a bacterial infection. Hence, IKK-beta is an important physiological contributor to the hypoxic response, linking it to innate immunity and inflammation.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-10353251, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-11085544, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-11595178, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-12390979, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-12529277, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-12628185, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-12692538, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15085193, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15122348, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15351965, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15630139, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15959903, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-15989949, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-16007254, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-16116163, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-16497588, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17047224, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17114296, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17402857, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17548584, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17803913, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-17956732, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-8387214, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-9091804, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-9436976, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-9545558, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-9606183, http://linkedlifedata.com/resource/pubmed/commentcorrection/18432192-9812940
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1476-4687
pubmed:author
pubmed:issnType
Electronic
pubmed:day
5
pubmed:volume
453
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
807-11
pubmed:dateRevised
2011-1-13
pubmed:meshHeading
pubmed:year
2008
pubmed:articleTitle
NF-kappaB links innate immunity to the hypoxic response through transcriptional regulation of HIF-1alpha.
pubmed:affiliation
Laboratory of Gene Regulation and Signal Transduction, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093-0723, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural