Abstract

Type I interferons (IFNs) are potent regulators of normal hematopoiesis in vitro and in vivo, but the mechanisms by which they suppress hematopoietic progenitor cell growth and differentiation are not known. In the present study we provide evidence that IFN alpha and IFN beta induce phosphorylation of the p38 mitogen-activated protein (Map) kinase in CD34+-derived primitive human hematopoietic progenitors. Such type I IFN-inducible phosphorylation of p38 results in activation of the catalytic domain of the kinase and sequential activation of the MAPK-activated protein kinase-2 (MapKapK-2 kinase), indicating the existence of a signaling cascade, activated downstream of p38 in hematopoietic progenitors. Our data indicate that activation of this signaling cascade by the type I IFN receptor is essential for the generation of the suppressive effects of type I IFNs on normal hematopoiesis. This is shown by studies demonstrating that pharmacological inhibitors of p38 reverse the growth inhibitory effects of IFN alpha and IFN beta on myeloid (colony-forming granulocytic-macrophage) and erythroid (burst-forming unit-erythroid) progenitor colony formation. In a similar manner, transforming growth factor beta, which also exhibits inhibitory effects on normal hematopoiesis, activates p38 and MapKapK-2 in human hematopoietic progenitors, whereas pharmacological inhibitors of p38 reverse its suppressive activities on both myeloid and erythroid colony formation. In further studies, we demonstrate that the primary mechanism by which the p38 Map kinase pathway mediates hematopoietic suppression is regulation of cell cycle progression and is unrelated to induction of apoptosis. Altogether, these findings establish that the p38 Map kinase pathway is a common effector for type I IFN and transforming growth factor beta signaling in human hematopoietic progenitors and plays a critical role in the induction of the suppressive effects of these cytokines on normal hematopoiesis.

Highlights

  • From the ‡Section of Hematology-Oncology and §Section of Rheumatology, Department of Medicine, University of Illinois at Chicago and West Side Veterans Affairs Medical Center, Chicago, Illinois 60607

  • These findings establish that the p38 mitogen-activated protein (Map) kinase pathway is a common effector for type I IFN and transforming growth factor ␤ signaling in human hematopoietic progenitors and plays a critical role in the induction of the suppressive effects of these cytokines on normal hematopoiesis

  • We demonstrate that TGF-␤, another potent inhibitor of normal hematopoiesis (27–32), activates p38 in progenitor cells and that pharmacological inhibitors of p38 reverse its suppressive effects on progenitor colony formation, indicating a critical role for this pathway in mediating myelosuppressive signals in human bone marrow cells

Read more

Summary

THE JOURNAL OF BIOLOGICAL CHEMISTRY

Vol 277, No 10, Issue of March 8, pp. 7726 –7735, 2002 Printed in U.S.A. Activation of the p38 Mitogen-activated Protein Kinase Mediates the Suppressive Effects of Type I Interferons and Transforming Growth Factor-␤ on Normal Hematopoiesis*. We demonstrate that the primary mechanism by which the p38 Map kinase pathway mediates hematopoietic suppression is regulation of cell cycle progression and is unrelated to induction of apoptosis These findings establish that the p38 Map kinase pathway is a common effector for type I IFN and transforming growth factor ␤ signaling in human hematopoietic progenitors and plays a critical role in the induction of the suppressive effects of these cytokines on normal hematopoiesis. We determined whether the p38 Map kinase pathway is engaged in type I IFN signaling in primary human hematopoietic progenitors and whether its function is required for the generation of the suppressive effects of interferons on normal hematopoiesis. We demonstrate that TGF-␤, another potent inhibitor of normal hematopoiesis (27–32), activates p38 in progenitor cells and that pharmacological inhibitors of p38 reverse its suppressive effects on progenitor colony formation, indicating a critical role for this pathway in mediating myelosuppressive signals in human bone marrow cells

EXPERIMENTAL PROCEDURES
RESULTS
DISCUSSION
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call