Interferon regulatory factor-2 protects quiescent hematopoietic stem cells from type I interferon–dependent exhaustion

T Sato, N Onai, H Yoshihara, F Arai, T Suda, T Ohteki - Nature medicine, 2009 - nature.com
T Sato, N Onai, H Yoshihara, F Arai, T Suda, T Ohteki
Nature medicine, 2009nature.com
Type I interferons (IFNs), a family of cytokines, orchestrate numerous biological and cellular
processes,,. Although it is well known that type I IFNs are essential for establishing the host
antiviral state, their role in hematopoietic homeostasis has not been studied. Here we show
that type I IFNs induce proliferation and exhaustion in hematopoietic stem cells (HSCs) and
that interferon regulatory factor-2 (IRF2), a transcriptional suppressor of type I IFN signaling,,
preserves the self-renewal and multilineage differentiation capacity of HSCs. HSCs were …
Abstract
Type I interferons (IFNs), a family of cytokines, orchestrate numerous biological and cellular processes,,. Although it is well known that type I IFNs are essential for establishing the host antiviral state, their role in hematopoietic homeostasis has not been studied. Here we show that type I IFNs induce proliferation and exhaustion in hematopoietic stem cells (HSCs) and that interferon regulatory factor-2 (IRF2), a transcriptional suppressor of type I IFN signaling,, preserves the self-renewal and multilineage differentiation capacity of HSCs. HSCs were substantially less abundant in the bone marrow of Irf2−/− as compared to Irf2+/− mice. Irf2−/− HSCs showed enhanced cell cycling status and failed to produce hematopoietic cells in competitive repopulation assays, and the reconstituting capacity of Irf2−/− HSCs was restored by disabling type I IFN signaling in these cells. In wild-type mice, injection of poly(I:C), an inducer of type I IFN signaling, or IFN-α induced HSC proliferation, and chronic type I IFN signaling further reduced the number of quiescent HSCs. Notably, combined poly(I:C) and 5-fluorouracil (5-FU) treatment allowed exogenous HSC engraftment and hematopoietic reconstitution in WT mice. Our findings provide insight into the molecular basis for the maintenance of HSC quiescence and may lead to improvements in bone marrow transplantation and type I IFN–based therapies for viral infection and cancer.
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