Skip to main content
Top
Published in: Obesity Surgery 4/2013

01-04-2013 | Clinical Research

Fibronectin Gene Expression in Human Adipose Tissue and Its Associations with Obesity-Related Genes and Metabolic Parameters

Authors: Seoung Hee Lee, Hye Soon Park, Jung Ah Lee, Young Sook Song, Yeon Jin Jang, Jong-Hyeok Kim, Yeon Ji Lee, Yoonseok Heo

Published in: Obesity Surgery | Issue 4/2013

Login to get access

Abstract

Background

Limited data are available on the in vivo expression of fibronectin, one of the main extracellular matrix components. We investigated the expression of fibronectin in abdominal visceral adipose tissue (VAT) and subcutaneous adipose tissue (SAT) and the associations of leptin, adiponectin, and vaspin gene expression with metabolic parameters in obese women.

Methods

We recruited female subjects undergoing bariatric surgery for obesity (n = 24) and patients undergoing benign gynecological surgery as the control group (n = 23). We measured anthropometric variables, abdominal fat distribution, metabolic parameters, serum concentrations of leptin, adiponectin, and vaspin, and depot-specific mRNA expression of fibronectin, leptin, adiponectin, and vaspin.

Results

Fibronectin expression in both VAT and SAT was significantly lower in the obese group than in the control group. Fibronectin expression in both VAT and SAT were negatively correlated with body mass index or waist circumference, with higher prominence in VAT. In multiple regression analysis, fibronectin expression in both VAT and SAT was negatively correlated with serum leptin concentration. Fibronectin expression in VAT was negatively correlated with leptin expression in VAT. Additionally, fibronectin expression in SAT was negatively correlated with leptin expression in SAT and positively correlated with adiponectin expression in VAT and SAT.

Conclusions

We found significant negative associations between depot-specific fibronectin expression in human adipose tissue and obesity indices and obesity-related biomarkers. Our results suggest that fibronectin expression may contribute to obesity and metabolic dysregulation in humans.
Literature
1.
go back to reference Adams JC, Watt FM. Fibronectin inhibits the terminal differentiation of human keratinocytes. Nature. 1989;340:307–9.PubMedCrossRef Adams JC, Watt FM. Fibronectin inhibits the terminal differentiation of human keratinocytes. Nature. 1989;340:307–9.PubMedCrossRef
2.
go back to reference Rutkowski JM, Davis KE, Scherer PE. Mechanisms of obesity and related pathologies: the macro- and microcirculation of adipose tissue. FEBS J. 2009;276:5738–46.PubMedCrossRef Rutkowski JM, Davis KE, Scherer PE. Mechanisms of obesity and related pathologies: the macro- and microcirculation of adipose tissue. FEBS J. 2009;276:5738–46.PubMedCrossRef
3.
go back to reference Pasarica M, Gowronska-Kozak B, Burk D, et al. Adipose tissue collagen VI in obesity. J Clin Endocrinol Metab. 2009;94:5155–62.PubMedCrossRef Pasarica M, Gowronska-Kozak B, Burk D, et al. Adipose tissue collagen VI in obesity. J Clin Endocrinol Metab. 2009;94:5155–62.PubMedCrossRef
4.
go back to reference Divoux A, Tordjman J, Lacasa D, et al. Fibrosis in human adipose tissue: composition, distribution, and link with lipid metabolism and fat mass loss. Diabetes. 2010;59:2817–25.PubMedCrossRef Divoux A, Tordjman J, Lacasa D, et al. Fibrosis in human adipose tissue: composition, distribution, and link with lipid metabolism and fat mass loss. Diabetes. 2010;59:2817–25.PubMedCrossRef
6.
go back to reference Antras J, Hilliou F, Redziniak G, et al. Decreased biosynthesis of actin and cellular fibronectin during adipose conversion of 3T3–F442A cells. Reorganization of the cytoarchitecture and extracellular matrix fibronectin. Biol Cell. 1989;66:247–54.PubMed Antras J, Hilliou F, Redziniak G, et al. Decreased biosynthesis of actin and cellular fibronectin during adipose conversion of 3T3–F442A cells. Reorganization of the cytoarchitecture and extracellular matrix fibronectin. Biol Cell. 1989;66:247–54.PubMed
7.
go back to reference Pierleoni C, Verdenelli F, Castellucci M, et al. Fibronectins and basal lamina molecules expression in human subcutaneous white adipose tissue. Eur J Histochem. 1998;42:183–8.PubMed Pierleoni C, Verdenelli F, Castellucci M, et al. Fibronectins and basal lamina molecules expression in human subcutaneous white adipose tissue. Eur J Histochem. 1998;42:183–8.PubMed
8.
go back to reference Taleb S, Cancello R, Clement K, et al. Cathepsin s promotes human preadipocyte differentiation: possible involvement of fibronectin degradation. Endocrinology. 2006;147:4950–9.PubMedCrossRef Taleb S, Cancello R, Clement K, et al. Cathepsin s promotes human preadipocyte differentiation: possible involvement of fibronectin degradation. Endocrinology. 2006;147:4950–9.PubMedCrossRef
9.
go back to reference Yoshizumi T, Nakamura T, Yamane M, et al. Abdominal fat: standardized technique for measurement at CT. Radiology. 1999;211:283–6.PubMed Yoshizumi T, Nakamura T, Yamane M, et al. Abdominal fat: standardized technique for measurement at CT. Radiology. 1999;211:283–6.PubMed
10.
go back to reference Matthews DR, Hosker JP, Rudenski AS, et al. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28:412–9.PubMedCrossRef Matthews DR, Hosker JP, Rudenski AS, et al. Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28:412–9.PubMedCrossRef
11.
go back to reference Novak M, Monkus E, Pardo V, et al. Preparation of subcellular fractions suitable for biochemical analyses from human subcutaneous adipose tissue obtained by needle biopsy. I. Isolation of mitochondria on a microscale. Exp Cell Res. 1972;73:335–44.PubMedCrossRef Novak M, Monkus E, Pardo V, et al. Preparation of subcellular fractions suitable for biochemical analyses from human subcutaneous adipose tissue obtained by needle biopsy. I. Isolation of mitochondria on a microscale. Exp Cell Res. 1972;73:335–44.PubMedCrossRef
12.
go back to reference Rodriguez Fernandez JL, Ben-Ze'ev A. Regulation of fibronectin, integrin and cytoskeleton expression in differentiating adipocytes: inhibition by extracellular matrix and polylysine. Differentiation. 1989;42:65–74.PubMedCrossRef Rodriguez Fernandez JL, Ben-Ze'ev A. Regulation of fibronectin, integrin and cytoskeleton expression in differentiating adipocytes: inhibition by extracellular matrix and polylysine. Differentiation. 1989;42:65–74.PubMedCrossRef
13.
go back to reference Spiegelman BM, Ginty CA. Fibronectin modulation of cell shape and lipogenic gene expression in 3T3–adipocytes. Cell. 1983;35:657–66.PubMedCrossRef Spiegelman BM, Ginty CA. Fibronectin modulation of cell shape and lipogenic gene expression in 3T3–adipocytes. Cell. 1983;35:657–66.PubMedCrossRef
14.
go back to reference Wang Y, Zhao L, Smas C, et al. Pref-1 interacts with fibronectin to inhibit adipocyte differentiation. Mol Cell Biol. 2010;30:3480–92.PubMedCrossRef Wang Y, Zhao L, Smas C, et al. Pref-1 interacts with fibronectin to inhibit adipocyte differentiation. Mol Cell Biol. 2010;30:3480–92.PubMedCrossRef
15.
go back to reference Hsieh P, Chen LB. Behavior of cells seeded in isolated fibronectin matrices. J Cell Biol. 1983;96:1208–17.PubMedCrossRef Hsieh P, Chen LB. Behavior of cells seeded in isolated fibronectin matrices. J Cell Biol. 1983;96:1208–17.PubMedCrossRef
16.
go back to reference Yamada KM, Yamada SS, Pastan I. Quantitation of a transformation-sensitive, adhesive cell surface glycoprotein. Decrease of several untransformed permanent cell lines. J Cell Biol. 1977;74:649–54.PubMedCrossRef Yamada KM, Yamada SS, Pastan I. Quantitation of a transformation-sensitive, adhesive cell surface glycoprotein. Decrease of several untransformed permanent cell lines. J Cell Biol. 1977;74:649–54.PubMedCrossRef
17.
go back to reference Spiegelman BM, Green H. Control of specific protein biosynthesis during the adipose conversion of 3T3 cells. J Biol Chem. 1980;255:8811–8.PubMed Spiegelman BM, Green H. Control of specific protein biosynthesis during the adipose conversion of 3T3 cells. J Biol Chem. 1980;255:8811–8.PubMed
18.
go back to reference Miller RE, Carrino DA. An association between glutamine synthetase activity and adipocyte differentiation in cultured 3T3–L1 cells. Arch Biochem Biophys. 1981;209:486–503.PubMedCrossRef Miller RE, Carrino DA. An association between glutamine synthetase activity and adipocyte differentiation in cultured 3T3–L1 cells. Arch Biochem Biophys. 1981;209:486–503.PubMedCrossRef
19.
go back to reference Steinberg MM, Brownstein BL. A clonal analysis of the differentiation of 3T3–L1 preadipose cells: role of insulin. J Cell Physiol. 1982;113:359–64.PubMedCrossRef Steinberg MM, Brownstein BL. A clonal analysis of the differentiation of 3T3–L1 preadipose cells: role of insulin. J Cell Physiol. 1982;113:359–64.PubMedCrossRef
20.
go back to reference Li Q, Hosaka T, Jambaldorj B, et al. Extracellular matrix with the rigidity of adipose tissue helps 3T3–L1 adipocytes maintain insulin responsiveness. J Med Investig. 2009;56:142–9.CrossRef Li Q, Hosaka T, Jambaldorj B, et al. Extracellular matrix with the rigidity of adipose tissue helps 3T3–L1 adipocytes maintain insulin responsiveness. J Med Investig. 2009;56:142–9.CrossRef
21.
go back to reference Zhang W, Ambati S, Della-Fera MA, et al. Leptin modulated changes in adipose tissue protein expression in ob/ob mice. Obesity (Silver Spring). 2011;19:255–61.CrossRef Zhang W, Ambati S, Della-Fera MA, et al. Leptin modulated changes in adipose tissue protein expression in ob/ob mice. Obesity (Silver Spring). 2011;19:255–61.CrossRef
Metadata
Title
Fibronectin Gene Expression in Human Adipose Tissue and Its Associations with Obesity-Related Genes and Metabolic Parameters
Authors
Seoung Hee Lee
Hye Soon Park
Jung Ah Lee
Young Sook Song
Yeon Jin Jang
Jong-Hyeok Kim
Yeon Ji Lee
Yoonseok Heo
Publication date
01-04-2013
Publisher
Springer-Verlag
Published in
Obesity Surgery / Issue 4/2013
Print ISSN: 0960-8923
Electronic ISSN: 1708-0428
DOI
https://doi.org/10.1007/s11695-012-0801-2

Other articles of this Issue 4/2013

Obesity Surgery 4/2013 Go to the issue