Open AccessREGULATION OF HUMAN MYELOPOIESIS BY PROSTAGLANDIN E AND LACTOFERRIN
Author(s) -
Pelus L. M.,
Broxmeyer H. E.,
Moore M. A. S.
Publication year - 1981
Publication title -
cell proliferation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.647
H-Index - 74
eISSN - 1365-2184
pISSN - 0960-7722
DOI - 10.1111/j.1365-2184.1981.tb00557.x
Subject(s) - myelopoiesis , prostaglandin e , progenitor cell , eosinophil , biology , lactoferrin , myeloid , monocyte , prostaglandin , peripheral blood mononuclear cell , cfu gm , colony forming unit , haematopoiesis , immunology , microbiology and biotechnology , biochemistry , stem cell , in vitro , bacteria , asthma , genetics
Studies on human myeloid stem cell proliferation indicate that progenitor cell populations committed to monocytoid differentiation are preferentially inhibited by prostaglandin E (PGE). the addition of PGE but not PGF to day 7 CFU GM cultures upon initiation results in the dose‐dependent inhibition of total colony and cluster formation. Morpholigical analysis of proliferating clones demonstrates that the effect of PGE on total colony and cluster formation results from the selective inhibition of monocyte‐macrophage colony forming cells. Mixed monocytoid/neutrophil colony formation was markedly less sensitive and neutrophil and eosinophil colony formation essentially insensitive to the inhibitory effects of PGE. the inhibition of monocytoid colony formation by PGE 1 extends equally well to day 13 CFU GM , but not to CFU GM in suspension culture. the observed effects of PGE 1 on monocytoid committed pre‐CFU GM and day 7 and day 14 CFU GM indicate that sensitivity to inhibition by PGE increases with progenitor cell maturity. Specificity analysis indicates that prostaglandins of the E series (PGE 1 , PGE 2 ) are by far the most active naturally occurring prostanoate compounds inhibiting CFU GM proliferation. The addition of iron saturated lactoferrin to liquid cultures of human peripheral blood monocytes, inclusion into mononuclear cell feeder layers or addition to agar cultures proliferating in response to endogenously produced CSFs, results in the equivalent inhibition of CSFs necessary for day 7 and day 14 monocytoid and/or neutrophil and eosinophil colony and cluster formation. These results indicate roles for PGE and lactoferrin in myeloid stem cell regulation in vitro and suggest that they may serve as physiological regulators of granulocyte and monocyte proliferation.