Source:http://linkedlifedata.com/resource/pubmed/id/12121221
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2002-7-17
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pubmed:abstractText |
Monocyte extravasation initiates reorganization of the cytoskeleton (CSK) and adhesion-dependent cytokine gene transcription. The actin CSK is thought to be crucial for compartmentalization and translation of mRNA, many of which contain AU-rich (ARE) instability motifs in the 3' untranslated region. We investigated regulation of adhesion-induced IL-1 beta expression by the monocyte CSK. In serum-free adherent monocytes, the induced IL-1 beta mRNA was stable and did not coextract with actin filaments. In contrast, in cells adherent in autologous serum, IL-1 beta transcripts were unstable, coextracted with actin filaments and were associated with only transient activation of the mitogen-activated protein kinases (MAPK). Under both conditions of adherence, the ARE-binding protein AUF1/hnRNP D was readily extracted in the cytosolic fraction. Electro-injection with AUF1/hnRNP D modified the actin CSK and, surprisingly, stabilized IL-1 beta transcripts. These data suggest that the control of mRNA degradation is linked with changes in the CSK. Mitogen-activated protein kinase activation or alterations in the availability of mRNA degradation factors may mediate these effects.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media,
http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Heterogeneous-Nuclear...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/hnRNP D0
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0818-9641
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
328-39
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:12121221-Actin Cytoskeleton,
pubmed-meshheading:12121221-Cell Adhesion,
pubmed-meshheading:12121221-Cells, Cultured,
pubmed-meshheading:12121221-Culture Media,
pubmed-meshheading:12121221-Cytoskeletal Proteins,
pubmed-meshheading:12121221-Heterogeneous-Nuclear Ribonucleoprotein D,
pubmed-meshheading:12121221-Humans,
pubmed-meshheading:12121221-Interleukin-1,
pubmed-meshheading:12121221-Intermediate Filaments,
pubmed-meshheading:12121221-Kinetics,
pubmed-meshheading:12121221-Mitogen-Activated Protein Kinases,
pubmed-meshheading:12121221-Monocytes,
pubmed-meshheading:12121221-RNA, Messenger,
pubmed-meshheading:12121221-RNA Stability,
pubmed-meshheading:12121221-RNA-Binding Proteins,
pubmed-meshheading:12121221-Signal Transduction,
pubmed-meshheading:12121221-Transcription, Genetic
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pubmed:year |
2002
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pubmed:articleTitle |
IL-1 beta transcript stability in monocytes is linked to cytoskeletal reorganization and the availability of mRNA degradation factors.
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pubmed:affiliation |
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, North Carolina, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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