Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1981-10-14
pubmed:abstractText
Experiments were designed to study the way in which normal human polymorphs (PMNs) inhibit the production or release of colony stimulating activity (CSA) by normal lymphocytes incubated alone or in conjunction with normal monocytes. PMNs were first incubated with lymphocytes for various periods at various concentrations. The PMNs were then removed and the 'conditioned' lymphocytes were used alone or after addition to adherent mononuclear cells (monocytes) for the production of conditioned medium. The samples of conditioned medium were then assayed for CSA in a standard system for culturing granulocyte/macrophage progenitor cells (CFU-C) in agar. We found that the capacity of PMNs to inhibit CSA production by lymphocytes or by lymphocytes plus monocytes was directly proportional to the number of PMNs originally incubated and maximal at relatively short incubation times (i.e. 2-4 h). Such inhibition could be counteracted by the introduction of known stimulators of CSA production by monocytes, e.g. phytohaemagglutinin or bacterial toxin. We conclude that normal lymphocytes 'conditioned' or 'programmed' by contact with PMNs may themselves have a reduced capacity to produce CSA and may also act to reduce CSA production by monocytes. Such programmed lymphocytes could thus be a component of the mechanism by which PMNs exert a physiological inhibition on CSA-dependent granulopoiesis in vivo.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
48
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
469-79
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:year
1981
pubmed:articleTitle
Autologous neutrophils inhibit production of colony stimulating activity by normal human lymphocytes.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't