期刊
BLOOD
卷 99, 期 12, 页码 4406-4412出版社
AMER SOC HEMATOLOGY
DOI: 10.1182/blood.V99.12.4406
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- NCI NIH HHS [CA72009] Funding Source: Medline
- NHLBI NIH HHS [HL56745] Funding Source: Medline
The CCAAT enhancer binding protein alpha (C/EBPalpha) transcription factor plays a critical role in granulocytopoiesis. Mice with a disruption of the C/EBPalpha gene demonstrate an early block in granulocytic differentiation, and disruption of C/EBPalpha function is a common theme in many types of human acute myelogenous leukemia, which is characterized by a block in myeloid development. To characterize further the nature of this block, we derived ell lines from the fetal liver of C/EBPalpha-deficient animals. These lines resembled morphologically the immature myeloid blasts observed in C/EBPalpha(-/-) fetal livers and did not express messenger RNA encoding early myeloid genes such as myeloperoxidase. Similarly, granulocytic markers such as Mac-1 and Gr-1 were not expressed; nor were erythroid and lymphoid surface antigens. Introduction of an inducible C/EBPalpha gene into the line revealed that conditional expression of C/EBPalpha induced the C/EBP family members C/EBPbeta and C/EBPepsilon and subsequent granulocyte differentiation. Similar results were obtained when C/EBPalpha(-/-) cells were stimulated with the cytokines interleukin-3 and granulocyte-macrophage colony-stimulating factor, but not with all-trans retinoic acid, supporting a model of at least 2 pathways leading to the differentiation of myeloid progenitors to granulocytes and implicating induction of other C/EBP family members in granulopoiesis. (C) 2002 by The American Society of Hematology.
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