Changes in vitamin D target gene expression in adipose tissue monitor the vitamin D response of human individuals. Issue 10 (28th July 2014)
- Record Type:
- Journal Article
- Title:
- Changes in vitamin D target gene expression in adipose tissue monitor the vitamin D response of human individuals. Issue 10 (28th July 2014)
- Main Title:
- Changes in vitamin D target gene expression in adipose tissue monitor the vitamin D response of human individuals
- Authors:
- Ryynänen, Jussi
Neme, Antonio
Tuomainen, Tomi‐Pekka
Virtanen, Jyrki K.
Voutilainen, Sari
Nurmi, Tarja
de Mello, Vanessa D. F.
Uusitupa, Matti
Carlberg, Carsten - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr2232-sec-0010" sec-type="section"> <title>Scope</title> <p>Vitamin D<sub>3</sub>, its biologically most active metabolite 1α, 25‐dihydroxyvitamin D<sub>3</sub> (1, 25(OH)<sub>2</sub>D<sub>3</sub>), and the vitamin D receptor (VDR) are important for adipose tissue biology.</p> </sec> <sec id="mnfr2232-sec-0020" sec-type="section"> <title>Methods and results</title> <p>We extrapolated genomic VDR association loci in adipocytes from 55 conserved genome‐wide VDR‐binding sites in nonfat tissues. Taking the genes <italic>DUSP10</italic>, <italic>TRAK1</italic>, <italic>NRIP1</italic>, and <italic>THBD</italic> as examples, we confirmed the predicted VDR binding sites upstream of their transcription start sites and showed rapid mRNA up‐regulation of all four genes in SGBS human pre‐adipocytes. Using adipose tissue biopsy samples from 47 participants of a 5‐month vitamin D<sub>3</sub> intervention study, we demonstrated that all four primary VDR target genes can serve as biomarkers for the vitamin D<sub>3</sub> responsiveness of human individuals. Changes in <italic>DUSP10</italic> gene expression appear to be the most comprehensive marker, while <italic>THBD</italic> mRNA changes characterized a rather different group of study participants.</p> </sec> <sec id="mnfr2232-sec-0030" sec-type="section"> <title>Conclusion</title> <p>We present a new approach to predict vitamin D target<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mnfr2232-sec-0010" sec-type="section"> <title>Scope</title> <p>Vitamin D<sub>3</sub>, its biologically most active metabolite 1α, 25‐dihydroxyvitamin D<sub>3</sub> (1, 25(OH)<sub>2</sub>D<sub>3</sub>), and the vitamin D receptor (VDR) are important for adipose tissue biology.</p> </sec> <sec id="mnfr2232-sec-0020" sec-type="section"> <title>Methods and results</title> <p>We extrapolated genomic VDR association loci in adipocytes from 55 conserved genome‐wide VDR‐binding sites in nonfat tissues. Taking the genes <italic>DUSP10</italic>, <italic>TRAK1</italic>, <italic>NRIP1</italic>, and <italic>THBD</italic> as examples, we confirmed the predicted VDR binding sites upstream of their transcription start sites and showed rapid mRNA up‐regulation of all four genes in SGBS human pre‐adipocytes. Using adipose tissue biopsy samples from 47 participants of a 5‐month vitamin D<sub>3</sub> intervention study, we demonstrated that all four primary VDR target genes can serve as biomarkers for the vitamin D<sub>3</sub> responsiveness of human individuals. Changes in <italic>DUSP10</italic> gene expression appear to be the most comprehensive marker, while <italic>THBD</italic> mRNA changes characterized a rather different group of study participants.</p> </sec> <sec id="mnfr2232-sec-0030" sec-type="section"> <title>Conclusion</title> <p>We present a new approach to predict vitamin D target genes based on conserved genomic VDR‐binding sites. Using human adipocytes as examples, we show that such ubiquitous VDR target genes can be used as markers for the individual's response to a supplementation with vitamin D<sub>3</sub>.</p> </sec> </abstract> … (more)
- Is Part Of:
- Molecular nutrition & food research. Volume 58:Issue 10(2014:Oct.)
- Journal:
- Molecular nutrition & food research
- Issue:
- Volume 58:Issue 10(2014:Oct.)
- Issue Display:
- Volume 58, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 58
- Issue:
- 10
- Issue Sort Value:
- 2014-0058-0010-0000
- Page Start:
- 2036
- Page End:
- 2045
- Publication Date:
- 2014-07-28
- Subjects:
- Food -- Biotechnology -- Periodicals
Food -- Microbiology -- Periodicals
Nutrition -- Periodicals
Food -- Toxicology -- Periodicals
Nutrition -- Periodicals
Food Microbiology -- Periodicals
Food Technology -- Periodicals
Molecular Biology -- Periodicals
664.0705 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/mnfr.201400291 ↗
- Languages:
- English
- ISSNs:
- 1613-4125
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817992
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3461.xml