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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0022688,
umls-concept:C0086418,
umls-concept:C0128897,
umls-concept:C0162326,
umls-concept:C0185117,
umls-concept:C0332256,
umls-concept:C0597357,
umls-concept:C1413188,
umls-concept:C1519595,
umls-concept:C1832554,
umls-concept:C1832555,
umls-concept:C1880022,
umls-concept:C2911684
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pubmed:issue |
6
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pubmed:dateCreated |
1997-4-2
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pubmed:databankReference | |
pubmed:abstractText |
NK cells migrate in response to C-C chemokines, including monocyte chemotactic protein-1 (MCP-1) and MCP-3. Increased migration was observed in IL-2-activated NK cells. It was therefore of interest to define the expression in resting and activated NK cells of the MCP-1 receptor (CCR2) for which two cDNAs (A and B) have been described. Specific oligonucleotides and reverse-transcriptase PCR revealed the presence in activated NK cells and mononuclear phagocytes of the fragments expected on the basis of the reported cDNAs. In addition, amplification with a common A/B- and an A-specific oligonucleotide yielded an unexpected, abundant, 1649-bp fragment. Sequence analysis as well as Northern blotting and RNase protection with different probes revealed that the CCR2 gene is expressed in activated NK cells and mononuclear phagocytes as a predominant long transcript (3.4 kb) consisting of CCR2B, followed by a novel sequence (X), corresponding to an intron in the genome, and by a CCR2A-specific portion. The predominant long transcript is polyadenylated and present in the cytoplasm. The augmented migratory capacity of IL-2 activated vs resting NK cells was associated with increased CCR2 transcript levels.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCR2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytokine
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
158
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2689-94
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9058802-Base Sequence,
pubmed-meshheading:9058802-Chemokine CCL2,
pubmed-meshheading:9058802-Cloning, Molecular,
pubmed-meshheading:9058802-Humans,
pubmed-meshheading:9058802-Interleukin-2,
pubmed-meshheading:9058802-Interphase,
pubmed-meshheading:9058802-Killer Cells, Natural,
pubmed-meshheading:9058802-Lymphocyte Activation,
pubmed-meshheading:9058802-Molecular Sequence Data,
pubmed-meshheading:9058802-Receptors, CCR2,
pubmed-meshheading:9058802-Receptors, Chemokine,
pubmed-meshheading:9058802-Receptors, Cytokine,
pubmed-meshheading:9058802-Transcription, Genetic
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pubmed:year |
1997
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pubmed:articleTitle |
IL-2-regulated expression of the monocyte chemotactic protein-1 receptor (CCR2) in human NK cells: characterization of a predominant 3.4-kilobase transcript containing CCR2B and CCR2A sequences.
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pubmed:affiliation |
Institute of Pharmacologic Research, Mario Negri, Milano, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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