Stem cells isolated from adipose tissue of obese patients show changes in their transcriptomic profile that indicate loss in stemcellness and increased commitment to an adipocyte-like phenotype


Por: Onate, B, Vilahur, G, Camino-Lopez, S, Diez-Caballero, A, Ballesta-Lopez, C, Ybarra, J, Moscatiello, F, Herrero, J, Badimon, L

Publicada: 16 sep 2013
Resumen:
Background: The adipose tissue is an endocrine regulator and a risk factor for atherosclerosis and cardiovascular disease when by excessive accumulation induces obesity. Although the adipose tissue is also a reservoir for stem cells (ASC) their function and "stemcellness"has been questioned. Our aim was to investigate the mechanisms by which obesity affects subcutaneous white adipose tissue (WAT) stem cells. Results: Transcriptomics, in silico analysis, real-time polymerase chain reaction (PCR) and western blots were performed on isolated stem cells from subcutaneous abdominal WAT of morbidly obese patients (ASCmo) and of non-obese individuals (ASCn). ASCmo and ASCn gene expression clustered separately from each other. ASCmo showed downregulation of "stemness"genes and upregulation of adipogenic and inflammatory genes with respect to ASCn. Moreover, the application of bioinformatics and Ingenuity Pathway Analysis (IPA) showed that the transcription factor Smad3 was tentatively affected in obese ASCmo. Validation of this target confirmed a significantly reduced Smad3 nuclear translocation in the isolated ASCmo. Conclusions: The transcriptomic profile of the stem cells reservoir in obese subcutaneous WAT is highly modified with significant changes in genes regulating stemcellness, lineage commitment and inflammation. In addition to body mass index, cardiovascular risk factor clustering further affect the ASC transcriptomic profile inducing loss of multipotency and, hence, capacity for tissue repair. In summary, the stem cells in the subcutaneous WAT niche of obese patients are already committed to adipocyte differentiation and show an upregulated inflammatory gene expression associated to their loss of stemcellness.

Filiaciones:
Onate, B:
 Hosp Santa Creu & Sant Pau, IIB St Pau, CSIC ICCC, Cardiovasc Res Ctr, Barcelona, Spain

Vilahur, G:
 Hosp Santa Creu & Sant Pau, IIB St Pau, CSIC ICCC, Cardiovasc Res Ctr, Barcelona, Spain

Camino-Lopez, S:
 Hosp Santa Creu & Sant Pau, IIB St Pau, CSIC ICCC, Cardiovasc Res Ctr, Barcelona, Spain

Diez-Caballero, A:
 Quirurg Cirujanos Asociados, Ctr Med Teknon, Barcelona, Spain

Ballesta-Lopez, C:
 CLB Ctr Laparoscop Doctor Ballesta, Barcelona, Spain

Ybarra, J:
 Resistencia Insulina SL, Barcelona, Spain

Moscatiello, F:
 Ctr Med Teknon, Dept Plast Surg, Barcelona, Spain

Herrero, J:
 Ctr Med Teknon, Dept Plast Surg, Barcelona, Spain

Badimon, L:
 Hosp Santa Creu & Sant Pau, IIB St Pau, CSIC ICCC, Cardiovasc Res Ctr, Barcelona, Spain
ISSN: 14712164





BMC GENOMICS
Editorial
BMC, CAMPUS, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 14 Número:
Páginas:
WOS Id: 000324755300002
ID de PubMed: 24040759
imagen Gold, Green Published

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