Human circulating CD14+ monocytes as a source of progenitors that exhibit mesenchymal cell differentiation

M Kuwana, Y Okazaki, H Kodama… - Journal of Leucocyte …, 2003 - academic.oup.com
M Kuwana, Y Okazaki, H Kodama, K Izumi, H Yasuoka, Y Ogawa, Y Kawakami, Y Ikeda
Journal of Leucocyte Biology, 2003academic.oup.com
Circulating CD14+ monocytes are precursors of phagocytes, such as macrophages and
dendritic cells. Here we report primitive cells with a fibroblast-like morphology derived from
human peripheral blood CD14+ monocytes that can differentiate into several distinct
mesenchymal cell lineages. We named this cell population monocyte-derived mesenchymal
progenitor (MOMP). MOMPs were obtained in vitro from human peripheral blood
mononuclear cells cultured on fibronectin in the presence of fetal bovine serum alone as a …
Abstract
Circulating CD14+ monocytes are precursors of phagocytes, such as macrophages and dendritic cells. Here we report primitive cells with a fibroblast-like morphology derived from human peripheral blood CD14+ monocytes that can differentiate into several distinct mesenchymal cell lineages. We named this cell population monocyte-derived mesenchymal progenitor (MOMP). MOMPs were obtained in vitro from human peripheral blood mononuclear cells cultured on fibronectin in the presence of fetal bovine serum alone as a source of growth factors. MOMPs had a unique molecular phenotype–CD14+CD45+CD34+ type I collagen+–and showed mixed morphologic and molecular features of monocytes and endothelial and mesenchymal cells. MOMPs were found to be derived from a subset of circulating CD14+ monocytes, and their differentiation required that they bind fibronectin and be exposed to one or more soluble factors derived from peripheral blood CD14 cells. MOMPs could be expanded in culture without losing their original phenotype for up to five passages. The induction of MOMPs to differentiate along multiple limb-bud mesodermal lineages resulted in the expression of genes and proteins specific for osteoblasts, skeletal myoblasts, chondrocytes, and adipocytes. Our findings represent the first evidence that human circulating CD14+ monocytes are a source of progenitors that exhibit mesenchymal cell differentiation.
Oxford University Press