Lipocalin 2 produces insulin resistance and can be upregulated by glucocorticoids in human adipose tissue

The adipokine lipocalin 2 is linked to obesity and metabolic disorders. However, its role in human adipose tissue glucose and lipid metabolism is not explored. Here we show that the synthetic glucocorticoid dexamethasone dose-dependently increased lipocalin 2 gene expression in subcutaneous and omen...

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Published inMolecular and cellular endocrinology Vol. 427; pp. 124 - 132
Main Authors Kamble, Prasad G., Pereira, Maria J., Sidibeh, Cherno O., Amini, Sam, Sundbom, Magnus, Börjesson, Joey Lau, Eriksson, Jan W.
Format Journal Article
LanguageEnglish
Published Ireland Elsevier Ireland Ltd 15.05.2016
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ISSN0303-7207
1872-8057
1872-8057
DOI10.1016/j.mce.2016.03.011

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Summary:The adipokine lipocalin 2 is linked to obesity and metabolic disorders. However, its role in human adipose tissue glucose and lipid metabolism is not explored. Here we show that the synthetic glucocorticoid dexamethasone dose-dependently increased lipocalin 2 gene expression in subcutaneous and omental adipose tissue from pre-menopausal females, while it had no effect in post-menopausal females or in males. Subcutaneous adipose tissue from both genders treated with recombinant human lipocalin 2 showed a reduction in protein levels of GLUT1 and GLUT4 and in glucose uptake in isolated adipocytes. In subcutaneous adipose tissue, lipocalin 2 increased IL-6 gene expression whereas expression of PPARγ and adiponectin was reduced. Our findings suggest that lipocalin 2 can contribute to insulin resistance in human adipose tissue. In pre-menopausal females, it may partly mediate adverse metabolic effects exerted by glucocorticoid excess. •This study demonstrates a role of lipocalin 2 in human adipose tissue metabolism.•Dexamethasone induces lipocalin 2 gene expression in pre-menopausal females.•Stromal vascular cells are major contributors of lipocalin 2 expression.•Lipocalin 2 impairs basal and insulin-stimulated glucose uptake in adipocytes.•Lipocalin 2 reduces PPARγ and adiponectin expression.
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ISSN:0303-7207
1872-8057
1872-8057
DOI:10.1016/j.mce.2016.03.011