Activation of Retinoid X Receptors Induces Apoptosis in HL-60 Cell Lines
Author(s) -
László Nagy,
Vilmos Thomázy,
Gregory L. Shipley,
László Fésüs,
William W. Lamph,
Richard A. Heyman,
Roshantha A.S. Chandraratna,
Peter J. Davies
Publication year - 1995
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.15.7.3540
Subject(s) - retinoid , retinoic acid , retinoid x receptor alpha , biology , receptor , retinoid x receptor , retinoid x receptor gamma , retinoic acid receptor alpha , retinoid x receptor beta , retinoic acid inducible orphan g protein coupled receptor , microbiology and biotechnology , retinoic acid receptor beta , tretinoin , retinoic acid receptor , nuclear receptor , cancer research , biochemistry , transcription factor , gene
Retinoids induce myeloblastic leukemia (HL-60) cells to differentiate into granulocytes, which subsequently die by apoptosis. Retinoid action is mediated through at least two classes of nuclear receptors: retinoic acid receptors, which bind both all-trans retinoic acid and 9-cis retinoic acid, and retinoid X receptors, which bind only 9-cis retinoic acid. Using receptor-selective synthetic retinoids and HL-60 cell sublines with different retinoid responsiveness, we have investigated the contribution that each class of receptors makes to the processes of cellular differentiation and death. Our results demonstrate that ligand activation of retinoic acid receptors is sufficient to induce differentiation, whereas ligand activation of retinoid X receptors is essential for the induction of apoptosis in HL-60 cell lines.
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