Cytokines stimulate granulopoiesis through signaling via receptors whose expression is controlled by lineage-specific transcription factors. Previously, we demonstrated that granulocyte colony-stimulating factor (G-CSF) receptor mRNA was undetectable and granulocyte maturation blocked in CCAAT enhancer binding protein α (C/EBPα)-deficient mice. This phenotype is distinct from that of G-CSF receptor−/− mice, suggesting that other genes are likely to be adversely affected by loss of C/EBPα. Here we demonstrate loss of interleukin 6 (IL-6) receptor and IL-6–responsive colony-forming units (CFU-IL6) in C/EBPα−/− mice. The observed failure of granulopoiesis could be rescued by the addition of soluble IL-6 receptor and IL-6 or by retroviral transduction of G-CSF receptors, demonstrating that loss of both of these receptors contributes to the absolute block in granulocyte maturation observed in C/EBPα-deficient hematopoietic cells. The results of these and other studies suggest that additional C/EBPα target genes, possibly other cytokine receptors, are also important for the block in granulocyte differentiation observed in vivo in C/EBPα-deficient mice.
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21 September 1998
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September 21 1998
Upregulation of Interleukin 6 and Granulocyte Colony-Stimulating Factor Receptors by Transcription Factor CCAAT Enhancer Binding Protein α (C/EBPα) Is Critical for Granulopoiesis
Pu Zhang,
Pu Zhang
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Atsushi Iwama,
Atsushi Iwama
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Milton W. Datta,
Milton W. Datta
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Gretchen J. Darlington,
Gretchen J. Darlington
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Daniel C. Link,
Daniel C. Link
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Daniel G. Tenen
Daniel G. Tenen
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
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Pu Zhang
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Atsushi Iwama
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Milton W. Datta
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Gretchen J. Darlington
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Daniel C. Link
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Daniel G. Tenen
From the *Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215; the ‡Department of Pathology and Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030; and the §Division of Bone Marrow Transplantation and Stem Cell Biology, Department of Medicine, Washington University Medical School, St. Louis, Missouri 63110-1093
Address correspondence to Daniel G. Tenen, Harvard Institutes of Medicine, Rm. 954, 77 Ave. Louis Pasteur, Boston, MA 02115. Phone: 617-667-5561; Fax: 617-667-3299; E-mail: [email protected]
Received:
May 06 1998
Revision Received:
June 29 1998
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1998
J Exp Med (1998) 188 (6): 1173–1184.
Article history
Received:
May 06 1998
Revision Received:
June 29 1998
Citation
Pu Zhang, Atsushi Iwama, Milton W. Datta, Gretchen J. Darlington, Daniel C. Link, Daniel G. Tenen; Upregulation of Interleukin 6 and Granulocyte Colony-Stimulating Factor Receptors by Transcription Factor CCAAT Enhancer Binding Protein α (C/EBPα) Is Critical for Granulopoiesis . J Exp Med 21 September 1998; 188 (6): 1173–1184. doi: https://doi.org/10.1084/jem.188.6.1173
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