Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.

BACKGROUND: Like other steroid hormones, vitamin D elicits both transcriptional events and rapid non genomic effects. Vitamin D receptor (VDR) localization and mechanisms of VDR-triggered non genomic responses are still controversial. Although anticoagulant effects of vitamin D have been reported an...

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Main Authors: Francesca Silvagno, Enrico De Vivo, Angelo Attanasio, Valentina Gallo, Gianna Mazzucco, Gianpiero Pescarmona
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2809087?pdf=render
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spelling doaj-8785f89e005948c1b8812f6b6cdec3332020-11-25T02:39:47ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-0151e867010.1371/journal.pone.0008670Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.Francesca SilvagnoEnrico De VivoAngelo AttanasioValentina GalloGianna MazzuccoGianpiero PescarmonaBACKGROUND: Like other steroid hormones, vitamin D elicits both transcriptional events and rapid non genomic effects. Vitamin D receptor (VDR) localization and mechanisms of VDR-triggered non genomic responses are still controversial. Although anticoagulant effects of vitamin D have been reported and VDR signalling has been characterized in monocytes and vascular cells, nothing is known about VDR expression and functions in human platelets, anucleated fragments of megakaryocytes which are known targets of other steroids. METHODOLOGY/PRINCIPAL FINDINGS: In this study we characterized the expression and cellular localization of VDR in human platelets and in a megakaryocyte lineage. Human platelets and their TPA-differentiated precursors expressed a classical 50 kDa VDR protein, which increased with megakaryocytes maturation. By biochemical fractionation studies we demonstrated the presence of the receptor in the soluble and mitochondrial compartment of human platelets, and the observation was confirmed by immunoelectron microscopy analysis. Similar localization was found in mature megakaryocytes, where besides its classical nuclear localization the receptor was evident as soluble and mitochondria resident protein. CONCLUSIONS: The results reported here suggest that megakaryocytopoiesis and platelet activation, which are calcium-dependent events, might be modulated by a mitochondrial non genomic activity of VDR. These data open challenging future studies on VDR physiological role in platelets and more generally in mitochondria.http://europepmc.org/articles/PMC2809087?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Francesca Silvagno
Enrico De Vivo
Angelo Attanasio
Valentina Gallo
Gianna Mazzucco
Gianpiero Pescarmona
spellingShingle Francesca Silvagno
Enrico De Vivo
Angelo Attanasio
Valentina Gallo
Gianna Mazzucco
Gianpiero Pescarmona
Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
PLoS ONE
author_facet Francesca Silvagno
Enrico De Vivo
Angelo Attanasio
Valentina Gallo
Gianna Mazzucco
Gianpiero Pescarmona
author_sort Francesca Silvagno
title Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
title_short Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
title_full Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
title_fullStr Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
title_full_unstemmed Mitochondrial localization of vitamin D receptor in human platelets and differentiated megakaryocytes.
title_sort mitochondrial localization of vitamin d receptor in human platelets and differentiated megakaryocytes.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-01-01
description BACKGROUND: Like other steroid hormones, vitamin D elicits both transcriptional events and rapid non genomic effects. Vitamin D receptor (VDR) localization and mechanisms of VDR-triggered non genomic responses are still controversial. Although anticoagulant effects of vitamin D have been reported and VDR signalling has been characterized in monocytes and vascular cells, nothing is known about VDR expression and functions in human platelets, anucleated fragments of megakaryocytes which are known targets of other steroids. METHODOLOGY/PRINCIPAL FINDINGS: In this study we characterized the expression and cellular localization of VDR in human platelets and in a megakaryocyte lineage. Human platelets and their TPA-differentiated precursors expressed a classical 50 kDa VDR protein, which increased with megakaryocytes maturation. By biochemical fractionation studies we demonstrated the presence of the receptor in the soluble and mitochondrial compartment of human platelets, and the observation was confirmed by immunoelectron microscopy analysis. Similar localization was found in mature megakaryocytes, where besides its classical nuclear localization the receptor was evident as soluble and mitochondria resident protein. CONCLUSIONS: The results reported here suggest that megakaryocytopoiesis and platelet activation, which are calcium-dependent events, might be modulated by a mitochondrial non genomic activity of VDR. These data open challenging future studies on VDR physiological role in platelets and more generally in mitochondria.
url http://europepmc.org/articles/PMC2809087?pdf=render
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