Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1993-11-24
pubmed:abstractText
We have tested whether breakdown of phosphatidylcholine (PC) initiated by exogenous addition of a PC-specific phospholipase C (PC-PLC) from Bacillus cereus or by endogenous overexpression of PC-PLC induces functional activation of NF-kappa B and increases human immunodeficiency virus (HIV) enhancer activity. PC-PLC-activated hydrolysis of PC was found to induce bona fide p50/p65 NF-kappa B binding activity in three different cell lines of human or murine origin. No significant changes in the turnover of other cellular phospholipids were detected in PC-PLC-treated cells. Induction of NF-kappa B by PC-PLC did not depend on de novo synthesis of proteins or autocrine secretion of either tumor necrosis factor or interleukin 1. In human monocytic and lymphoblastoid T-cell lines, induction of NF-kappa B by PC-PLC resulted in clear induction of luciferase expression vectors placed under the control of synthetic kappa B enhancers or wild type, but not kappa B-mutated, HIV long terminal repeat constructs. HIV replication was increased by PC-PLC in chronically infected monocytes and T lymphocytes. NF-kappa B activation promoted by addition of exogenous PC-PLC correlated with an intense production of diacylglycerol. However, addition of a phosphatidylinositol-specific PLC from B. cereus also induced diacylglycerol but did not activate kappa B enhancer-directed vectors. PC-PLC-induced NF-kappa B activation could not be blocked by a specific inhibitor of phorbol ester-inducible protein kinases C. These results indicate that a cellular transduction pathway, dependent on specific PC breakdown, is functional in T lymphocytes and monocytes and may be used by various transmembrane receptors to activate HIV transcription through NF-kappa B-dependent induction of the HIV enhancer.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1455508, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1502202, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1639070, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1658188, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1839358, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1845988, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-1874734, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2006423, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2023633, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2023953, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2104616, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2112426, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2123453, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2146676, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2157987, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2186905, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2203531, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2315321, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2470089, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2477457, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2506180, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2574206, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2576770, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2682462, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2825351, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-2898301, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-3031512, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-3140380, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-3313065, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-3462727, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-3510743, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-6270351, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-8336714, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-8423794, http://linkedlifedata.com/resource/pubmed/commentcorrection/8411362-8424175
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
67
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6596-604
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Phosphatidylcholine hydrolysis activates NF-kappa B and increases human immunodeficiency virus replication in human monocytes and T lymphocytes.
pubmed:affiliation
Unite d'Immunologie Virale, Institut Pasteur, Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't