TY - JOUR
T1 - C/EBPβ is required for survival of Ly6C- monocytes
AU - Tamura, Akihiro
AU - Hirai, Hideyo
AU - Yokota, Asumi
AU - Kamio, Naoka
AU - Sato, Atsushi
AU - Shoji, Tsukimi
AU - Kashiwagi, Takahiro
AU - Torikoshi, Yusuke
AU - Miura, Yasuo
AU - Tenen, Daniel G.
AU - Maekawa, Taira
N1 - Publisher Copyright:
© 2017 by The American Society of Hematology.
PY - 2017/10/19
Y1 - 2017/10/19
N2 - The transcription factor CCAAT/enhancer-binding protein β (C/EBPβ) is highly expressed in monocytes/macrophages. However, its roles inmonopoiesis are largely unknown. Here, we investigated the roles of C/EBPβ in monopoiesis. Further subdivision of monocytes revealed that Cebpb messenger RNA was highly upregulated in Ly6C- monocytes in bone marrow. Accordingly, the number of Ly6C- monocytes was significantly reduced in Cebpb-/- mice. Bonemarrow chimera experiments and Mx1-Cre-mediated deletion of Cebpbrevealed a cellintrinsic and monocyte-specific requirement for C/EBPβ in monopoiesis. In Cebpb-/- mice, turnover of Ly6C- monocytes was highly accelerated and apoptosis of Ly6C- monocytes was increased. Expression of Csf1r, which encodes a receptor for macrophage colonystimulating factor, was significantly reducedin Ly6C- monocytes of Cebpb-/- mice. C/EBPβ bound to positive regulatory elements of Csf1r and promoted its transcription. Collectively, these results indicate that C/EBPβ is a critical factor for Ly6C- monocyte survival, at least in part through upregulation of Csf1r.
AB - The transcription factor CCAAT/enhancer-binding protein β (C/EBPβ) is highly expressed in monocytes/macrophages. However, its roles inmonopoiesis are largely unknown. Here, we investigated the roles of C/EBPβ in monopoiesis. Further subdivision of monocytes revealed that Cebpb messenger RNA was highly upregulated in Ly6C- monocytes in bone marrow. Accordingly, the number of Ly6C- monocytes was significantly reduced in Cebpb-/- mice. Bonemarrow chimera experiments and Mx1-Cre-mediated deletion of Cebpbrevealed a cellintrinsic and monocyte-specific requirement for C/EBPβ in monopoiesis. In Cebpb-/- mice, turnover of Ly6C- monocytes was highly accelerated and apoptosis of Ly6C- monocytes was increased. Expression of Csf1r, which encodes a receptor for macrophage colonystimulating factor, was significantly reducedin Ly6C- monocytes of Cebpb-/- mice. C/EBPβ bound to positive regulatory elements of Csf1r and promoted its transcription. Collectively, these results indicate that C/EBPβ is a critical factor for Ly6C- monocyte survival, at least in part through upregulation of Csf1r.
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U2 - 10.1182/blood-2017-03-772962
DO - 10.1182/blood-2017-03-772962
M3 - Review article
C2 - 28807982
AN - SCOPUS:85032175059
SN - 0006-4971
VL - 130
SP - 1809
EP - 1818
JO - Blood
JF - Blood
IS - 16
ER -