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Biosynthesis of ferritin subunits from different cell lines of HL-60 human promyelocytic leukaemia cells and the release of acidic isoferritin-inhibitory activity against normal granulocyte-macrophage progenitor cells.

Abstract
Biosynthesis of acidic isoferritins was investigated in human promyelocytic HL-60 cells, characterized by diploid (2C), tetraploid (4C) and mixed diploid--tetraploid (2C-4C) DNA cell lines. The three cell lines were studied for the biosynthesis of ferritin and its subunits and for the release of acidic isoferritin-inhibitory activity against normal CFU-GM before and after addition of DMSO. While the tetraploid and mixed diploid--tetraploid cell lines synthesized more H-(Mr = 21) than L-subunits (Mr = 19) after induction, the tetraploid line synthesized more H-subunit before and after induction, compared to the diploid line. The release of acidic isoferritin-inhibitory activity was greater before than after induction in both cell lines, but the tetraploid cell line released more acidic isoferritin-inhibitory activity consistent with its greater production of Mr = 21 subunit. However, after induction no inhibitory activity could be detected from the diploid cells and much less activity was detected with the tetraploid cells, suggesting that differentiation caused a decrease in production of acidic isoferritin-inhibitory activity.
AuthorsM H Dörner, H E Broxmeyer, A Silverstone, M Andreeff
JournalBritish journal of haematology (Br J Haematol) Vol. 55 Issue 1 Pg. 47-58 (Sep 1983) ISSN: 0007-1048 [Print] England
PMID6576806 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Ferritins
  • Dimethyl Sulfoxide
Topics
  • Animals
  • Cell Line
  • Colony-Forming Units Assay
  • Dimethyl Sulfoxide (pharmacology)
  • Ferritins (biosynthesis, pharmacology)
  • Granulocytes (drug effects)
  • Hematopoietic Stem Cells (drug effects)
  • Humans
  • Leukemia, Experimental (metabolism)
  • Leukemia, Myeloid, Acute (metabolism)
  • Macrophages (drug effects)
  • Peptide Biosynthesis
  • Ploidies

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