Temporal Changes in Gene Expression Profile during Mature Adipocyte Dedifferentiation

Author:

Côté Julie Anne123,Guénard Frédéric34,Lessard Julie1,Lapointe Marc1,Biron Simon1,Vohl Marie-Claude34ORCID,Tchernof André123ORCID

Affiliation:

1. Centre de Recherche de l’Institut Universitaire de Cardiologie et de Pneumologie de Québec, 2725 Chemin Ste-Foy, Quebec City, QC, Canada G1V 4G5

2. Centre de Recherche du CHU de Québec, 2705 Boulevard Laurier, Quebec City, QC, Canada G1V 4G2

3. École de Nutrition, Université Laval, 2425 Rue de l’Agriculture, Quebec City, QC, Canada G1V 0A6

4. Institut sur la Nutrition et les Aliments Fonctionnels (INAF), 2440 Boulevard Hochelaga, Quebec City, QC, Canada G1V 0A6

Abstract

Objective. To characterize changes in gene expression profile during human mature adipocyte dedifferentiation in ceiling culture.Methods. Subcutaneous (SC) and omental (OM) adipose tissue samples were obtained from 4 participants paired for age and BMI. Isolated adipocytes were dedifferentiated in ceiling culture. Gene expression analysis at days 0, 4, 7, and 12 of the cultures was performed using Affymetrix Human Gene 2.0 STvi arrays. Hierarchical clustering according to similarity of expression changes was used to identify overrepresented functions.Results. Four clusters gathered genes with similar expression between day 4 to day 7 but decreasing expression from day 7 to day 12. Most of these genes coded for proteins involved in adipocyte functions (LIPE,PLIN1,DGAT2,PNPLA2,ADIPOQ,CEBPA,LPL,FABP4,SCD,INSR, andLEP). Expression of several genes coding for proteins implicated in cellular proliferation and growth or cell cycle increased significantly from day 7 to day 12 (WNT5A,KITLG, andFGF5). Genes coding for extracellular matrix proteins were differentially expressed between days 0, 4, 7, and 12 (COL1A1,COL1A2, andCOL6A3,MMP1, andTGFB1).Conclusion. Dedifferentiation is associated with downregulation of transcripts encoding proteins involved in mature adipocyte functions and upregulation of genes involved in matrix remodeling, cellular development, and cell cycle.

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Hindawi Limited

Subject

Pharmaceutical Science,Genetics,Molecular Biology,Biochemistry

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