Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2004-8-5
pubmed:abstractText
Several ligands for Toll IL-1R (TIR) family are known to promote stabilization of a subset of short-lived mRNAs containing AU-rich elements (AREs) in their 3' untranslated regions. It is now evident however, that members of the TIR family may use distinct intracellular signaling pathways to achieve a spectrum of biological end points. Using human embryonic kidney 293 cells transfected to express different TIRs we now report that signals initiated through IL-1R1 or TLR4 but not TLR3 can promote the stabilization of unstable chemokine mRNAs. Similar results were obtained when signaling from endogenous receptors was examined using a mouse endothelial cell line (H5V). The ability of TIR family members to stabilize ARE-containing mRNAs results from their differential use of signaling adaptors MyD88, MyD88 adaptor-like protein, Toll receptor IFN-inducing factor (Trif), and Trif-related adaptor molecule. Overexpression of MyD88 or MyD88 adaptor-like protein was able to promote enhanced stability of ARE-containing mRNA, whereas Trif and Trif-related adaptor molecule exhibited markedly reduced capacity. Hence the ability of TIRs to signal stabilization of mRNA appears to be linked to the MyD88-dependent signaling pathway.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/3' Untranslated Regions, http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing, http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Vesicular..., http://linkedlifedata.com/resource/pubmed/chemical/Adenosine, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation, http://linkedlifedata.com/resource/pubmed/chemical/Chemokines, http://linkedlifedata.com/resource/pubmed/chemical/MYD88 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Myd88 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Myeloid Differentiation Factor 88, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-1 Type I, http://linkedlifedata.com/resource/pubmed/chemical/TIRAP protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TLR3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TLR4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptor 3, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptor 4, http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptors, http://linkedlifedata.com/resource/pubmed/chemical/Uridine
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
173
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2755-61
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15294994-3' Untranslated Regions, pubmed-meshheading:15294994-Adaptor Proteins, Signal Transducing, pubmed-meshheading:15294994-Adaptor Proteins, Vesicular Transport, pubmed-meshheading:15294994-Adenosine, pubmed-meshheading:15294994-Animals, pubmed-meshheading:15294994-Antigens, Differentiation, pubmed-meshheading:15294994-Blotting, Western, pubmed-meshheading:15294994-Cell Line, pubmed-meshheading:15294994-Chemokines, pubmed-meshheading:15294994-Humans, pubmed-meshheading:15294994-In Situ Hybridization, pubmed-meshheading:15294994-Membrane Glycoproteins, pubmed-meshheading:15294994-Myeloid Differentiation Factor 88, pubmed-meshheading:15294994-RNA, Messenger, pubmed-meshheading:15294994-Receptors, Cell Surface, pubmed-meshheading:15294994-Receptors, Immunologic, pubmed-meshheading:15294994-Receptors, Interleukin-1, pubmed-meshheading:15294994-Receptors, Interleukin-1 Type I, pubmed-meshheading:15294994-Signal Transduction, pubmed-meshheading:15294994-Toll-Like Receptor 3, pubmed-meshheading:15294994-Toll-Like Receptor 4, pubmed-meshheading:15294994-Toll-Like Receptors, pubmed-meshheading:15294994-Transfection, pubmed-meshheading:15294994-Uridine
pubmed:year
2004
pubmed:articleTitle
Toll IL-1 receptors differ in their ability to promote the stabilization of adenosine and uridine-rich elements containing mRNA.
pubmed:affiliation
Department of Immunology, Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S.