Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P04141 (
granulocyte-macrophage colony-stimulating factor
)
6,790
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Interleukin-13
(
IL-13
) is a pleiotropic cytokine that inhibits the production of inflammatory cytokines of monocytes. We investigated the effects of
IL-13
on the clonal growth of human hematopoietic progenitors.
IL-13
alone did not support any colony formation.
IL-13
markedly suppressed macrophage colonies that were formed in the presence of IL-3 and erythropoietin,
granulocyte-macrophage colony-stimulating factor
, or macrophage colony-stimulating factor. Macrophage colony cells showed dendritic cell-line morphology and cellular aggregates.
IL-13
did not affect granulocyte colony and erythroid burst formation. Delayed addition of
IL-13
and replating onto the culture dishes with
IL-13
showed that macrophage colony formation was suppressed during days 8 and 14 of culture. These results indicate that
IL-13
affects the growth of the late stage of committed macrophage progenitors. Single-cell culture of isolated CD34+CD33+ cells with
IL-13
confirmed that macrophage colony formation was significantly suppressed. These results show that
IL-13
directly suppresses the proliferation of differentiating macrophages. In addition, these suppressive effects of
IL-13
were synergistic with IL-4. Furthermore, in the liquid culture of bone marrow cells in the presence of
IL-13
, the number of CD14 (monocyte-macrophage antigen)-positive cells decreased and CD18 (LFA-1 beta)-positive cells increased. It is concluded that
IL-13
affects the growth of the late stage of macrophage precursors as well as mature monocytes. Induction of differentiation of human monocytes may be correlated with the suppression of their progenitors.
...
PMID:Interleukin-13 selectively suppresses the growth of human macrophage progenitors at the late stage. 778 Jan 35