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Article

Diverse Regulation of Vitamin D Receptor Gene Expression by 1,25-Dihydroxyvitamin D and ATRA in Murine and Human Blood Cells at Early Stages of Their Differentiation

1
Laboratory of Molecular and Cellular Immunology, Department of Tumor Immunology, Institute of Immunology and Experimental Therapy, Polish Academy of Science, Weigla 12, 53-114 Wrocław, Poland
2
Laboratory of Protein Biochemistry, Faculty of Biotechnology, University of Wrocław, Joliot-Curie 14a, 50-383 Wrocław, Poland
3
First Department of Obstetrics and Gynecology, Wrocław Medical University, Chałubińskiego 3, 50-368 Wrocław, Poland
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Academic Editor: Anthony Lemarié
Int. J. Mol. Sci. 2017, 18(6), 1323; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061323
Received: 2 May 2017 / Revised: 1 June 2017 / Accepted: 14 June 2017 / Published: 21 June 2017
(This article belongs to the Special Issue The Biology and Treatment of Myeloid Leukaemias)
Vitamin D receptor (VDR) is present in multiple blood cells, and the hormonal form of vitamin D, 1,25-dihydroxyvitamin D (1,25D) is essential for the proper functioning of the immune system. The role of retinoic acid receptor α (RARα) in hematopoiesis is very important, as the fusion of RARα gene with PML gene initiates acute promyelocytic leukemia where differentiation of the myeloid lineage is blocked, followed by an uncontrolled proliferation of leukemic blasts. RARα takes part in regulation of VDR transcription, and unliganded RARα acts as a transcriptional repressor to VDR gene in acute myeloid leukemia (AML) cells. This is why we decided to examine the effects of the combination of 1,25D and all-trans-retinoic acid (ATRA) on VDR gene expression in normal human and murine blood cells at various steps of their development. We tested the expression of VDR and regulation of this gene in response to 1,25D or ATRA, as well as transcriptional activities of nuclear receptors VDR and RARs in human and murine blood cells. We discovered that regulation of VDR expression in humans is different from in mice. In human blood cells at early stages of their differentiation ATRA, but not 1,25D, upregulates the expression of VDR. In contrast, in murine blood cells 1,25D, but not ATRA, upregulates the expression of VDR. VDR and RAR receptors are present and transcriptionally active in blood cells of both species, especially at early steps of blood development. View Full-Text
Keywords: blood cells; vitamin D receptor; retinoic acid receptors; expression; CYP24A1; CYP26A1; differentiation; hematopoietic stem cells blood cells; vitamin D receptor; retinoic acid receptors; expression; CYP24A1; CYP26A1; differentiation; hematopoietic stem cells
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MDPI and ACS Style

Janik, S.; Nowak, U.; Łaszkiewicz, A.; Satyr, A.; Majkowski, M.; Marchwicka, A.; Śnieżewski, Ł.; Berkowska, K.; Gabryś, M.; Cebrat, M.; Marcinkowska, E. Diverse Regulation of Vitamin D Receptor Gene Expression by 1,25-Dihydroxyvitamin D and ATRA in Murine and Human Blood Cells at Early Stages of Their Differentiation. Int. J. Mol. Sci. 2017, 18, 1323. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061323

AMA Style

Janik S, Nowak U, Łaszkiewicz A, Satyr A, Majkowski M, Marchwicka A, Śnieżewski Ł, Berkowska K, Gabryś M, Cebrat M, Marcinkowska E. Diverse Regulation of Vitamin D Receptor Gene Expression by 1,25-Dihydroxyvitamin D and ATRA in Murine and Human Blood Cells at Early Stages of Their Differentiation. International Journal of Molecular Sciences. 2017; 18(6):1323. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061323

Chicago/Turabian Style

Janik, Sylwia; Nowak, Urszula; Łaszkiewicz, Agnieszka; Satyr, Anastasiia; Majkowski, Michał; Marchwicka, Aleksandra; Śnieżewski, Łukasz; Berkowska, Klaudia; Gabryś, Marian; Cebrat, Małgorzata; Marcinkowska, Ewa. 2017. "Diverse Regulation of Vitamin D Receptor Gene Expression by 1,25-Dihydroxyvitamin D and ATRA in Murine and Human Blood Cells at Early Stages of Their Differentiation" Int. J. Mol. Sci. 18, no. 6: 1323. https://0-doi-org.brum.beds.ac.uk/10.3390/ijms18061323

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