Journal of Biological Chemistry · 1997 · 30 citations · 58 references
Life SciencesCell BiologyGeneticsCell PhysiologyCell ProliferationCell SignalingAnimal Cell CultureCytokine BiologyHematopoietic DevelopmentHematopoietic DifferentiationHematopoietic Stem Cell BiologyLymphocyte DevelopmentBone Marrow - Derived CellsCytokine Signaling In HematopoiesisDifferentiation Of Hematopoietic ProgenitorsErythroid Lineage CommitmentHematopoietic Stem Cell DifferentiationMegakaryocyte Differentiation
There are numerous similarities between the erythroid and megakaryocytic lineages which suggest that commitment to either lineage occurs relatively late in hematopoiesis. Commitment toward megakaryocyte development requires obligatory silencing of erythroid-specific genes. Therefore, we investigated the effects of interleukin-6, a known inducer of thrombocyte production, on globin gene expression during erythroid differentiation. Studies in K562 cells demonstrated inhibition of gamma globin gene mRNA production and chain biosynthesis in the presence of exogenous interleukin-6 which was abrogated by anti-interleukin-6 monoclonal antibody. Similar studies in primary erythroid progenitors showed inhibition of burst-forming unit-erythroid colony formation when interleukin-6 was added late in cultures with decreased gamma and beta globin gene mRNA production. Protein binding studies demonstrated an increase in activator protein-1 binding to its consensus sequence by 24 h of interleukin-6 treatment. Inhibition of activator protein-1 gene activity had no effect on gamma gene silencing by interleukin-6. A potential interleukin-6 response element was identified in the gamma globin gene. Interleukin-6 treatment led to a rapid increase in protein binding to the target DNA sequence. These results suggest that interleukin-6 may play an important role in globin gene silencing during megakaryocytic lineage commitment.
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Jack Gauldie, Carl D. Richards, D.C. Harnish et al. · Proceedings of the National Academy of Sciences · 1987 · 1.7K citations · Full text
Life Sciences, Immunology, Pathology +15
The c-fos protein interacts with c-JunAP-1 to stimulate transcription of AP-1 responsive genes
Robert Chiu, William J. Boyle, Jennifer Meek et al. · Cell · 1988 · 1.4K citations · Full text