The role of G-CSF and IL-6 in the granulopoiesis-stimulating activity of murine blood serum induced by perorally administered ultrafiltered pig leukocyte extract, IMUNOR
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17386413
DOI
10.1016/j.intimp.2007.01.011
PII: S1567-5769(07)00030-6
Knihovny.cz E-resources
- MeSH
- Immune Sera pharmacology MeSH
- Cell Extracts MeSH
- Stimulation, Chemical MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Granulocyte Colony-Stimulating Factor antagonists & inhibitors physiology MeSH
- Granulocytes physiology MeSH
- Hematopoiesis drug effects MeSH
- Interleukin-3 antagonists & inhibitors MeSH
- Interleukin-6 antagonists & inhibitors physiology MeSH
- Bone Marrow drug effects metabolism MeSH
- Leukocytes physiology MeSH
- Antibodies, Monoclonal pharmacology MeSH
- Mice MeSH
- Swine MeSH
- Antibodies, Blocking pharmacology MeSH
- Tissue Extracts pharmacology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Immune Sera MeSH
- Cell Extracts MeSH
- Granulocyte Colony-Stimulating Factor MeSH
- IMUNOR MeSH Browser
- Interleukin-3 MeSH
- Interleukin-6 MeSH
- Antibodies, Monoclonal MeSH
- Antibodies, Blocking MeSH
- Tissue Extracts MeSH
IMUNOR, a low-molecular weight (< 12 kD) ultrafiltered pig leukocyte extract, has been previously found to have significant stimulatory effects on murine hematopoiesis supressed by ionizing radiation or cytotoxic drugs. This communication shows data on the mechanisms of these effects. Using ELISA assay, significantly increased levels of granulocyte colony-stimulating factor (G-CSF) and interleukin-6 (IL-6) were observed. On the contrary, no detectable levels of granulocyte-macrophage colony-stimulating factor (GM-CFC) and interleukin-3 (IL-3) have been found in blood serum of IMUNOR-treated mice. Incubation of the serum from IMUNOR-treated mice with antibodies against G-CSF caused abrogation of the ability of the sera to stimulate in vitro growth of colonies originating from granulocyte-macrophage progenitor cells (GM-CFC). In contrast, incubation of the serum with antibodies against IL-6 did not change its colony-stimulating activity. It may be inferred from these findings that G-CSF is probably the main cytokine responsible for the granulopoiesis-stimulating effects of IMUNOR. When the serum from IMUNOR-treated mice with G-CSF inactivated by anti-G-CSF antibodies (but with elevated IL-6) was added to cultures of bone marrow cells together with a suboptimum concentration of IL-3, a significant increase in the numbers of GM-CFC colonies was found. Moreover, conjoint inactivation of G-CSF and IL-6 significantly decreased the numbers of GM-CFC colonies in comparison with those observed when only G-CSF was inactivated. This observation strongly suggests that though IMUNOR-induced IL-6 is not able to induce the growth of GM-CFC colonies alone, it is able to potentiate the hematopoiesis-stimulating effect of IL-3. These findings represent a new knowledge concerning the hematopoiesis-stimulating action of IMUNOR, a promising immunomodulatory agent.
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