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The kit receptor and its ligand, steel factor, as regulators of hemopoiesis.
Broxmeyer, H E; Maze, R; Miyazawa, K; Carow, C; Hendrie, P C; Cooper, S; Hangoc, G; Vadhan-Raj, S; Lu, L.
Affiliation
  • Broxmeyer HE; Department of Medicine (Hematology/Oncology), Indiana University School of Medicine, Indianapolis 46202.
Cancer Cells ; 3(12): 480-7, 1991 Dec.
Article in En | MEDLINE | ID: mdl-1726456
ABSTRACT
Mouse strains carrying mutations at the Dominant White Spotting (W) locus or the Steel (Sl) locus are anemic and display defects in pigmentation and gametogenesis. In W mutants the anemia is due to a deficiency of hemopoietic stem cells and, in Sl mutants, to a deficiency of supporting stromal cells in the bone marrow. The W locus encodes the c-kit proto-oncogene product, a cell surface receptor with protein-tyrosine kinase activity, and the Sl locus encodes its ligand, a hemopoietic cytokine known variously as Steel factor (SLF), mast cell growth factor, stem cell factor, and Kit ligand. SLF can synergize with a number of other cytokines to stimulate growth of hemopoietic progenitors in vitro and stimulates blood cell production in vivo in animals. Here we review the biological activities of SLF, with particular emphasis on its effects on hemopoietic stem and progenitor cells. We also discuss present knowledge of the molecules involved in SLF-triggered signal transduction, and speculate on potential therapeutic applications for SLF in human disease.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Cell Growth Factors / Proto-Oncogene Proteins / Hematopoiesis Language: En Journal: Cancer Cells Journal subject: NEOPLASIAS Year: 1991 Document type: Article
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Cell Growth Factors / Proto-Oncogene Proteins / Hematopoiesis Language: En Journal: Cancer Cells Journal subject: NEOPLASIAS Year: 1991 Document type: Article