Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/11802
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Título : Differential proteomics of omental and subcutaneous adipose tissue reflects their unalike biochemical and metabolic properties
Autor : Pérez-Pérez, Rafael, Ortega, Francisco J., García-Santos, Eva, López, Juan A., Camafeita, Emilio, Ricart, Wifredo, Fernández-Real, José M., Peral, Belén
Palabras clave : Obesity
Adipose tissue
Omental fat
Subcutaneous fat
Mesothelial cells
Metabolic syndrome
2D-DIGE
Proteomics
MALDI-TOF/TOF
Fecha de publicación : 9-Feb-2009
Editor: American Chemical Society
Resumen: Obesity is increasing exponentially in developed countries and constitutes a public health problem by enhancing the risk for metabolic disorder and cardiovascular disease. Differences in gene expression profiles and in metabolic and biochemical properties have been well-described between omental and subcutaneous adipose tissue in humans. Because omental adipose tissue has been strongly associated with the development of insulin resistance, type 2 diabetes and cardiovascular disease, we searched for proteins differentially expressed in these two fat depots using two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) and mass spectrometry (MS). In this analysis, we found 43 proteins, several of which were validated by immunoblotting and immunostaining analyses. Results demonstrated tissue-specific molecular differences in the protein makeup of the two analyzed fat depots mainly related to metabolic processes such as glucose and lipid metabolism, lipid transport, protein synthesis, protein folding, response to stress and inflammation. This suggests higher metabolic activity as well as increased cell stress in the omental compared to the subcutaneous fat. These findings provide some insights into the role of omental fat in abdominal obesity-associated co-morbidities.
Descripción : 12 pages, 6 figures.-- PMID: 19203289 [PubMed].-- Article in press.
Versión del editor: http://dx.doi.org/10.1021/pr800942k
URI : http://hdl.handle.net/10261/11802
ISSN: 1535-3893
DOI: 10.1021/pr800942k
Citación : Journal of Proteome Research (2009), doi: 10.1021/pr800942k
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