Linked Life Data

8473736

Source:http://linkedlifedata.com/resource/pubmed/id/8473736

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
1993-5-20
pubmed:abstractText
In T cells, signals initiated at the TCR, and in particular activation of protein kinase C (PKC), can activate the p21ras proteins. Triggering of the TCR and PKC is required for the efficient production of the T cell growth factor, IL-2. IL-2 gene transcription is controlled by a 275-bp enhancer that is known to contain binding sites for many transcription factors including the octamer family of proteins, NF kappa B, AP-1, and a T cell-specific factor, NFAT (nuclear factor of activated T cells). NFAT binds to a region of the IL-2 enhancer that has been defined as a TCR response element (ARRE-2), and is induced in response to increases in intracellular calcium, stimulation of PKC, or triggering of the TCR. To determine whether p21ras is involved in the signals that regulate NFAT, we examined the effect of expression of a constitutively active p21ras mutant, v-Ha-ras, and a dominant inhibitory mutant of p21ras, c-Ha-ras(asn)17, on the induction of a NFAT-driven reporter gene (NFAT CAT) during T cell activation. The constitutively active Ras mutant could synergize with the calcium ionophore ionomycin to induce NFAT. In addition, expression of p21v-Ha-ras could enhance NFAT CAT induction in response to TCR and PKC agonists. The dominant inhibitory mutant of p21ras could prevent NFAT CAT expression in response to PKC or TCR triggering. These data show that Ras regulates NFAT, and that p21ras function is important for the TCR- and PKC-regulated pathways that regulate NFAT.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0022-1767
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
150
pubmed:geneSymbol
v-Ha-ras
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3853-61
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
p21ras function is important for T cell antigen receptor and protein kinase C regulation of nuclear factor of activated T cells.
pubmed:affiliation
Lymphocyte Activation Laboratory, Imperial Cancer Research Fund, London, United Kingdom.
pubmed:publicationType
Journal Article