4.2 Article

Visfatin expression analysis in association with recruitment and activation of human and rodent brown and brite adipocytes

Journal

ADIPOCYTE
Volume 5, Issue 2, Pages 186-195

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21623945.2015.1122854

Keywords

hMADS; nampt; obesity; PBEF; type 2 diabetes; UCP1

Funding

  1. CNRS
  2. INSERM
  3. Universite de Nice Sophia Antipolis
  4. EU FP7 project DIABAT [HEALTH-F2-2011-278373]
  5. French Agence Nationale de la Recherche [ANR-10-BLAN-1105, ANR-RPV12004AAA-DiamiR]
  6. Aviesan/AstraZeneca
  7. Diabetes and the vessel wall injury program
  8. Investments for the Future LABEX SIG-NALIFE [ANR-11-LABX-0028-01]
  9. European Foundation for the Study of Diabetes (EFSD/Lilly
  10. European Diabetes Research Program)
  11. European Foundation for the Study of Diabetes [Lilly 2014_6] Funding Source: researchfish
  12. Agence Nationale de la Recherche (ANR) [ANR-10-BLAN-1105] Funding Source: Agence Nationale de la Recherche (ANR)

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Human brown adipocytes are able to burn fat and glucose and are now considered as a potential strategy to treat obesity, type 2 diabetes and metabolic disorders. Besides their thermogenic function, brown adipocytes are able to secrete adipokines. One of these is visfatin, a nicotinamide phosphoribosyltransferase involved in nicotinamide dinucleotide synthesis, which is known to participate in the synthesis of insulin by pancreatic b cells. In a therapeutic context, it is of interest to establish whether a potential correlation exists between brown adipocyte activation and/or brite adipocyte recruitment, and adipokine expression. We analyzed visfatin expression, as a pre-requisite to its secretion, in rodent and human biopsies and cell models of brown/brite adipocytes. We found that visfatin was preferentially expressed in mature adipocytes and that this expression was higher in brown adipose tissue of rodents compared to other fat depots. However, using various rodent models we were unable to find any correlation between visfatin expression and brown or brite adipocyte activation or recruitment. Interestingly, the situation is different in humans where visfatin expression was found to be equivalent between white and brown or brite adipocytes in vivo and in vitro. In conclusion, visfatin can be considered only as a rodent brown adipocyte biomarker, independently of tissue activation.

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