Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1989-9-25
pubmed:abstractText
Exposure of cultured human peripheral blood monocytes (PBMO) to interferon-gamma (IFN-gamma) enhances surface expression of the p55 subunit of the interleukin-2 receptor (IL-2R). Addition of IL-2 to IFN-gamma treated monocytes will stimulate subsequent release of interleukin-1 beta (IL-1 beta) and tumour necrosis factor-alpha (TNF-alpha) due to enhancement of the transcriptional rate and stability of mRNA accumulation of both genes. The present study was aimed to investigate whether IFN-gamma and IL-2 will favour the release of IL-1 beta and TNF-alpha by different subsets of human PBMO. To this end PBMO were separated into four fractions with densities ranging from 1.058 to 1.075 kg/l by means of discontinuous bovine serum albumin (BSA) gradient centrigugation. Following incubation of monocyte subsets in the presence or absence of IFN-gamma and IL-2 for a culture period of 24-48 h, cell-free culture supernatants were collected and assayed for IL-1 beta and TNF-alpha activity by ELISA. Surface p55 IL-2R expression was detected by CD25 monoclonal antibody (MoAb) anti-IL-2R1 using immunofluorescence analysis. Although IL-2R1 expressing PBMO were equally distributed among the four fractions, IL-1 beta secretion was found to reside mainly in the most dense fraction. The major TNF-alpha activity was detected, however, in supernatants obtained from cultures of PBMO with densities of 1.065-1.075 kg/l. These data demonstrate functional heterogeneity of subsets of human PBMO with respect to their capacity to produce distinct cytokines.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-2452833, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-2467700, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-2474236, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-2920210, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3010124, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3102073, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3102253, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3138311, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3262679, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-3499192, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-6603982, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-6606726, http://linkedlifedata.com/resource/pubmed/commentcorrection/2504521-6806370
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0009-9104
pubmed:author
pubmed:issnType
Print
pubmed:volume
77
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
97-100
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
1989
pubmed:articleTitle
Interleukin-2 and interferon-gamma recruit different subsets of human peripheral blood monocytes to secrete interleukin-1 beta and tumour necrosis factor-alpha.
pubmed:affiliation
Department of Haematology, Johannes Gutenberg-University of Mainz, FRG.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't