TRANSFORMING GROWTH FACTOR-BETA DIRECTLY REGULATES PRIMITIVE MURINE HEMATOPOIETIC-CELL PROLIFERATION

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  • 1 February 1990
    • journal article
    • research article
    • Vol. 75  (3) , 596-602
Abstract
We previously reported that transforming growth factor .beta. (TGF-.beta.) selectively inhibits colony-stimulating factor-driven hematopoietic progenitor cell growth. We report here that TGF-.beta.1 can act directly on hematopoietic progenitors to inhibit the growth of the most primitive progenitors measureable in vitro. Highly enriched populations of hematopoietic cells were obtained by isolating lineage negative (Lin-), Thy-1-positive (Thy-1+) fresh bone marrow cells, or by isolating cells from interleukin-3 (IL-3) supplemented bone marrow cultures expressing Thy-1 antigen with the fluorescent activated cell sorter. TGF-.beta.1 inhibited IL-3-induced Thy-1 expression on Thy-1-negative (Thy-1-) bone marrow cells in a dose-dependent manner with an ED50 of 5 to 10 pmol/l. In addition, TGF-.beta.1 inhibited the formation of multipotent and mixed colonies by isolated Thy-1+ cells, while single lineage granulocyte and macrophage colonies were not affected. The growth of Thy-1+ Lin- cells incubated as single cells in Terasaki plates in medium supplemented with IL-3 were inhibited by TGF-.beta., demonstrating a direct inhibitory effect. Hematopoietic stem cells, which have a high proliferative potential (HPP) when responding to combinations of growth factors in vitro, have been detected in the bone marrow of normal mice and mice surviving a single injection of 5-fluorouracil. TGF-.beta.1 inhibited the growth of all subpopulations of HPP colony forming cells (CFC) in a dose-dependent manner with an ED50 of 5 to 10 PMOL/L. Thus, TGF-.beta. directly inhibits the growth of the most immature hematopoietic cells measureable in vitro.