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Comparative Study
. 2004 Jun;47(6):1118-25.
doi: 10.1007/s00125-004-1417-4. Epub 2004 May 28.

Expression of fatty-acid-handling proteins in human adipose tissue in relation to obesity and insulin resistance

Affiliations
Comparative Study

Expression of fatty-acid-handling proteins in human adipose tissue in relation to obesity and insulin resistance

K Gertow et al. Diabetologia. 2004 Jun.

Abstract

Aims/hypothesis: Protein-mediated trans-membrane and intracellular fatty acid trafficking are becoming increasingly recognised as biochemically and physiologically important concepts. Obesity and insulin resistance are polygenic disorders, heavily influenced by environmental and life-style factors, and are virtually always associated with disturbed fatty acid metabolism in adipose and other tissues. The aim of this study was to investigate mRNA expression levels of fatty-acid-handling proteins in adipose tissue in relation to markers of genetic and acquired obesity and insulin resistance.

Methods: We quantified mRNA expression of subcutaneous adipose tissue fatty-acid-handling proteins (ALBP, KLBP, FATP1, FATP4, CD36, ACS1) in 17 monozygotic twin-pairs with a range of intra-pair differences (Delta) in BMI and detailed measures of obesity and insulin resistance, allowing influences of genetic and non-genetic factors to be distinguished.

Results: In acquired obesity FATP4 expression was up-regulated independently of genetic background (DeltaFATP4 versus DeltaBMI; r=0.50, p=0.04; DeltaFATP4 versus Deltabody fat; r=0.59, p=0.01). Similarly, CD36 and FATP1 expression correlated with acquired differences in HDL cholesterol and non-esterified fatty acid concentrations respectively. Moreover, FATP4 and CD36 expression levels correlated with measures of obesity and insulin resistance that are influenced by both genetic and non-genetic factors (FATP4 versus BMI: r=0.53, p=0.0001; FATP4 versus body fat: r=0.51, p=0.002; FATP4 versus homeostasis model assessment [HOMA]: r=0.49, p=0.001; CD36 versus BMI: r=0.50, p=0.02; CD36 versus body fat: r=0.63, p=0.001; CD36 versus HOMA: r=0.34, p=0.06).

Conclusions/interpretation: These findings indicate that expression of specific adipose tissue fatty-acid-handling proteins is related to obesity and insulin resistance, and that, in particular, FATP4 plays a role in acquired obesity. Our results suggest that facilitated fatty acid trafficking is a physiologically and pathologically relevant phenomenon in man.

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References

    1. Diabetes. 2003 Feb;52(2):300-7 - PubMed
    1. AIDS. 2003 Aug 15;17 (12 ):1753-62 - PubMed
    1. Biochim Biophys Acta. 1998 Apr 22;1391(3):287-306 - PubMed
    1. Proc Natl Acad Sci U S A. 1980 May;77(5):2542-5 - PubMed
    1. Trends Endocrinol Metab. 2001 Aug;12(6):266-73 - PubMed

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