Hyporesponsiveness of murine myeloid progenitor cells to glucan following its repeated administration
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
8187896
Knihovny.cz E-zdroje
- MeSH
- adjuvancia imunologická farmakologie MeSH
- aktivace makrofágů * MeSH
- analýza kolonii tvořících jednotek MeSH
- beta-glukany * MeSH
- diklofenak farmakologie MeSH
- faktory stimulující kolonie biosyntéza MeSH
- glukany farmakologie MeSH
- granulocyty účinky léků patologie MeSH
- hematopoetické kmenové buňky účinky léků patologie MeSH
- hyperplazie MeSH
- kostní dřeň patologie MeSH
- myši inbrední C57BL MeSH
- myši inbrední CBA MeSH
- myši MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adjuvancia imunologická MeSH
- beta-1,3-glucan MeSH Prohlížeč
- beta-glukany * MeSH
- diklofenak MeSH
- faktory stimulující kolonie MeSH
- glukany MeSH
A moderate marrow granulocytic hyperplasia developed after 4 injections of glucan (soluble derivative carboxymethylglucan) administered to mice at 3-4-day intervals. However, when evaluating the response of the marrow granulocyte-macrophage colony-forming cells (GM-CFC) to the fifth glucan injection given in the repetitive treatment schedule, the development of hyporesponsiveness of these cells was found, contrary to the stimulatory action of a single glucan injection. In addition, the prompt increase in serum granulocyte-macrophage colony-stimulating activity occurring after a single glucan injection, and proposed to upregulate myelopoiesis, was absent in mice treated with glucan repeatedly. A joint administration of glucan with diclofenac, an inhibitor of prostaglandin synthesis, was able to enhance the GM-CFC response to a single glucan injection, probably due to the removal of the downregulation action of prostaglandins on these progenitor cells. However, a repeated administration of diclofenac with glucan did not reduce substantially the development of GM-CFC hyporesponsiveness. Thus, the results suggest that the GM-CFC hyporesponsiveness or tolerance to repeated glucan injections was induced by weakening the mechanisms of positive control mediated by the serum colony-stimulating activity.
Modulation of animal and human hematopoiesis by β-glucans: a review