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J Exp Med ; 214(7): 1901-1912, 2017 Jul 03.
Article in English | MEDLINE | ID: mdl-28550162

ABSTRACT

Prolonged exit from quiescence by hematopoietic stem cells (HSCs) progressively impairs their homeostasis in the bone marrow through an unidentified mechanism. We show that Rb proteins, which are major enforcers of quiescence, maintain HSC homeostasis by positively regulating thrombopoietin (Tpo)-mediated Jak2 signaling. Rb family protein inactivation triggers the progressive E2f-mediated transactivation of Socs3, a potent inhibitor of Jak2 signaling, in cycling HSCs. Aberrant activation of Socs3 impairs Tpo signaling and leads to impaired HSC homeostasis. Therefore, Rb proteins act as a central hub of quiescence and homeostasis by coordinating the regulation of both cell cycle and Jak2 signaling in HSCs.


Subject(s)
Hematopoietic Stem Cells/metabolism , Homeostasis/genetics , Retinoblastoma Protein/genetics , Retinoblastoma-Like Protein p107/genetics , Retinoblastoma-Like Protein p130/genetics , Suppressor of Cytokine Signaling 3 Protein/genetics , Animals , Cell Cycle/genetics , Cell Division/genetics , Cell Proliferation/genetics , E2F Transcription Factors/genetics , E2F Transcription Factors/metabolism , Gene Expression Profiling/methods , Immunoblotting , Janus Kinase 2/genetics , Janus Kinase 2/metabolism , Mice, Knockout , Mice, Transgenic , Phosphorylation/drug effects , RNA Interference , Retinoblastoma Protein/metabolism , Retinoblastoma-Like Protein p107/metabolism , Retinoblastoma-Like Protein p130/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Suppressor of Cytokine Signaling 3 Protein/metabolism , Thrombopoietin/pharmacology , Transcriptional Activation
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