Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1994-10-20
|
pubmed:abstractText |
Recently, we have shown that T cells exposed to concentrations of prostaglandin E2 (PGE2) or the beta-adrenergic receptor agonist isoproterenol (ISO) that elicit equimolar levels of cAMP accumulation do not inhibit anti-CD3 monoclonal antibody-induced T cell proliferation to the same extent. This report extends these studies by investigating the induction of cAMP-dependent protein kinase (PKA) in T cells stimulated with PGE2 or ISO. The kinetics of PKA activity induced by PGE2 or ISO in T cells are similar but PGE2 induces more PKA activity. When T cells were treated with concentrations of PGE2 or ISO that elicited similar PKA activities, PGE2 was found to be more immunosuppressive than ISO. T cells stimulated with PGE2 or ISO showed similar levels of increased PKA activity in both the cytosolic and the particulate fractions. Quantitation of the activity of PKA I and PKA II isozymes in T cells stimulated with PGE2 or ISO revealed that both types were activated; however, while PGE2 induced the utilization of an equal amount of both isozymes in T cells, ISO-treated cells utilized twice as much PKA I compared to PKA II. Overall, these results suggest that qualitative differences in the concentration of cAMP and PKA activity are important elements in modulatory T cell proliferative responses.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP-Dependent Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Isoproterenol,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, beta,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Prostaglandin E
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0008-8749
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
158
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
182-94
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:8087864-Antibodies, Monoclonal,
pubmed-meshheading:8087864-Antigens, CD3,
pubmed-meshheading:8087864-Cell Compartmentation,
pubmed-meshheading:8087864-Cells, Cultured,
pubmed-meshheading:8087864-Cyclic AMP,
pubmed-meshheading:8087864-Cyclic AMP-Dependent Protein Kinases,
pubmed-meshheading:8087864-Dinoprostone,
pubmed-meshheading:8087864-Enzyme Activation,
pubmed-meshheading:8087864-Enzyme Induction,
pubmed-meshheading:8087864-Humans,
pubmed-meshheading:8087864-Isoenzymes,
pubmed-meshheading:8087864-Isoproterenol,
pubmed-meshheading:8087864-Kinetics,
pubmed-meshheading:8087864-Lymphocyte Activation,
pubmed-meshheading:8087864-Receptors, Adrenergic, beta,
pubmed-meshheading:8087864-Receptors, Prostaglandin E,
pubmed-meshheading:8087864-T-Lymphocytes
|
pubmed:year |
1994
|
pubmed:articleTitle |
Induction of cAMP-dependent protein kinase (PKA) activity in T cells after stimulation of the prostaglandin E2 or the beta-adrenergic receptors: relationship between PKA activity and inhibition of anti-CD3 monoclonal antibody-induced T cell proliferation.
|
pubmed:affiliation |
Department of Microbiology and Immunology, University of Kentucky Medical Center, Lexington 40536-0084.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|