Proposal of a bioinformatics approach to predict molecular mechanisms involved in inflammatory response: case of ATRA and 1, 25(OH)2D in adipocytes. Issue 1 (31st December 2023)
- Record Type:
- Journal Article
- Title:
- Proposal of a bioinformatics approach to predict molecular mechanisms involved in inflammatory response: case of ATRA and 1, 25(OH)2D in adipocytes. Issue 1 (31st December 2023)
- Main Title:
- Proposal of a bioinformatics approach to predict molecular mechanisms involved in inflammatory response: case of ATRA and 1, 25(OH)2D in adipocytes
- Authors:
- Karkeni, Esma
Payet, Thomas
Astier, Julien
Sicard, Flavie
Mounien, Lourdes
Landrier, Jean-François - Abstract:
- ABSTRACT: Several inflammatory markers such as cytokines, chemokines, and microRNAs (miRNAs) are well known to be induced during obesity and are strongly linked to their comorbidities. Among many others factors, the micronutrient status is suspected to reduce obesity-associated inflammation via blunting inflammatory signalling pathways. This is notably the case for active forms of vitamin A (all-trans retinoic acid ATRA) and vitamin D (1, 25(OH)2 D) as previously shown. In the present study, we aimed to implement a new bioinformatics approach to unveil commonly regulated signalling pathways through a combination of gene and miRNA expression sets impacted by ATRA and 1, 25(OH)2 D in adipocytes. In a first set of experiments, we focused only our attention on ATRA and demonstrated that it reduced LPS-mediated miRNA expression (miR-146a, miR-150, and miR-155) in mouse adipose tissue, in adipocyte cultures, and in adipocyte-derived vesicles. This result was confirmed in TNFα-induced miRNA in human adipocytes. Then, bioinformatic analysis highlighted that both ATRA and 1, 25(OH)2 D-regulated genes and miRNA converge to the canonical 'nuclear factor Kappa B (NF-κB) signalling pathway.' Altogether, these results showed that ATRA has anti-inflammatory effects on miRNA expression. In addition, the proposed bioinformatic model converges to NF-κB signalling pathway that has been previously demonstrated to be regulated by ATRA and 1, 25(OH)2 D, thus confirming the interest of suchABSTRACT: Several inflammatory markers such as cytokines, chemokines, and microRNAs (miRNAs) are well known to be induced during obesity and are strongly linked to their comorbidities. Among many others factors, the micronutrient status is suspected to reduce obesity-associated inflammation via blunting inflammatory signalling pathways. This is notably the case for active forms of vitamin A (all-trans retinoic acid ATRA) and vitamin D (1, 25(OH)2 D) as previously shown. In the present study, we aimed to implement a new bioinformatics approach to unveil commonly regulated signalling pathways through a combination of gene and miRNA expression sets impacted by ATRA and 1, 25(OH)2 D in adipocytes. In a first set of experiments, we focused only our attention on ATRA and demonstrated that it reduced LPS-mediated miRNA expression (miR-146a, miR-150, and miR-155) in mouse adipose tissue, in adipocyte cultures, and in adipocyte-derived vesicles. This result was confirmed in TNFα-induced miRNA in human adipocytes. Then, bioinformatic analysis highlighted that both ATRA and 1, 25(OH)2 D-regulated genes and miRNA converge to the canonical 'nuclear factor Kappa B (NF-κB) signalling pathway.' Altogether, these results showed that ATRA has anti-inflammatory effects on miRNA expression. In addition, the proposed bioinformatic model converges to NF-κB signalling pathway that has been previously demonstrated to be regulated by ATRA and 1, 25(OH)2 D, thus confirming the interest of such approach. … (more)
- Is Part Of:
- Epigenetics. Volume 18:Issue 1(2023)
- Journal:
- Epigenetics
- Issue:
- Volume 18:Issue 1(2023)
- Issue Display:
- Volume 18, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 18
- Issue:
- 1
- Issue Sort Value:
- 2023-0018-0001-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-12-31
- Subjects:
- NF-κB -- bioinformatics -- adipocytes -- adipose tissue -- vitamins -- vitamin a -- vitamin D
Epigenesis -- Periodicals
Epigenetica
572.86505 - Journal URLs:
- http://www.landesbioscience.com/journals/epigenetics/ ↗
http://www.tandfonline.com/toc/kepi20/current ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1080/15592294.2023.2201516 ↗
- Languages:
- English
- ISSNs:
- 1559-2294
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3793.650300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26935.xml