Hyporesponsiveness of murine myeloid progenitor cells to glucan following its repeated administration
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
8187896
Knihovny.cz E-resources
- MeSH
- Adjuvants, Immunologic pharmacology MeSH
- Macrophage Activation * MeSH
- Colony-Forming Units Assay MeSH
- beta-Glucans * MeSH
- Diclofenac pharmacology MeSH
- Colony-Stimulating Factors biosynthesis MeSH
- Glucans pharmacology MeSH
- Granulocytes drug effects pathology MeSH
- Hematopoietic Stem Cells drug effects pathology MeSH
- Hyperplasia MeSH
- Bone Marrow pathology MeSH
- Mice, Inbred C57BL MeSH
- Mice, Inbred CBA MeSH
- Mice MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Adjuvants, Immunologic MeSH
- beta-1,3-glucan MeSH Browser
- beta-Glucans * MeSH
- Diclofenac MeSH
- Colony-Stimulating Factors MeSH
- Glucans 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