Regulation of granulocyte‐macrophage colony‐stimulating factor and interleukin 3 expression Journal Article


Authors: Nimer, S. D.; Uchida, H.
Article Title: Regulation of granulocyte‐macrophage colony‐stimulating factor and interleukin 3 expression
Abstract: Granulocyte‐macrophage colony stimulating factor (GM‐CSF) and interleukin 3 (IL‐3) are multilineage acting hematopoietic growth factors which have overlapping but distinct biological properties. Cellular sources of IL‐3 are confined to activated T cells, natural killer (NK) cells, mast cells and possibly megakaryocytes, while these cells and activated macrophages, fibroblasts and endothelial cells are important sources of GM‐CSF. In vitro studies have implicated both cytokines in the autocrine growth of human myeloid or murine mast cell leukemias. The human GM‐CSF and IL‐3 genes map to the long arm of chromosome 5, show similar genomic structures, and share several conserved elements in their 5′ and 3′ flanking regions. The promoters of these genes contain a variety of positive and negative regulatory regions, and the level of expression of these genes is controlled by both transcriptional and post‐transcriptional mechanisms. Copyright © 1995 AlphaMed Press
Keywords: leukemia; review; t cells; t lymphocyte; t-lymphocytes; granulocyte macrophage colony stimulating factor; gene expression regulation; dna; transcription regulation; molecular sequence data; natural killer cell; base sequence; dna flanking region; megakaryocyte; gene location; gene structure; chromosomal localization; autocrine growth; gene regulation; mast cell; mast cells; granulocyte-macrophage colony-stimulating factor; chromosome 5q; promoter regions (genetics); interleukin 3; interleukin-3; promoter analysis; human leukemia; human; support, non-u.s. gov't; support, u.s. gov't, p.h.s.; gm‐csf; il‐3
Journal Title: Stem Cells
Volume: 13
Issue: 4
ISSN: 1066-5099
Publisher: AlphaMed Press  
Date Published: 1995-01-01
Start Page: 324
End Page: 335
Language: English
DOI: 10.1002/stem.5530130402
PUBMED: 7549890
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 28 August 2018 -- Source: Scopus
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  1. Stephen D Nimer
    347 Nimer