Dysregulation of the expression and secretion of inflammation-related adipokines by hypoxia in human adipocytes

B Wang, IS Wood, P Trayhurn - Pflügers Archiv-European Journal of …, 2007 - Springer
B Wang, IS Wood, P Trayhurn
Pflügers Archiv-European Journal of Physiology, 2007Springer
The effect of hypoxia, induced by incubation under low (1%) oxygen tension or by exposure
to CoCl 2, on the expression and secretion of inflammation-related adipokines was
examined in human adipocytes. Hypoxia led to a rapid and substantial increase (greater
than sevenfold by 4 h of exposure to 1% O 2) in the hypoxia-sensitive transcription factor,
HIF-1α, in human adipocytes. This was accompanied by a major increase (up to 14-fold) in
GLUT1 transporter mRNA level. Hypoxia (1% O 2 or CoCl 2) led to a reduction (up to …
Abstract
The effect of hypoxia, induced by incubation under low (1%) oxygen tension or by exposure to CoCl2, on the expression and secretion of inflammation-related adipokines was examined in human adipocytes. Hypoxia led to a rapid and substantial increase (greater than sevenfold by 4 h of exposure to 1% O2) in the hypoxia-sensitive transcription factor, HIF-1α, in human adipocytes. This was accompanied by a major increase (up to 14-fold) in GLUT1 transporter mRNA level. Hypoxia (1% O2 or CoCl2) led to a reduction (up to threefold over 24 h) in adiponectin and haptoglobin mRNA levels; adiponectin secretion also decreased. No changes were observed in TNFα expression. In contrast, hypoxia resulted in substantial increases in FIAF/angiopoietin-like protein 4, IL-6, leptin, MIF, PAI-1 and vascular endothelial growth factor (VEGF) mRNA levels. The largest increases were with FIAF (maximum 210-fold), leptin (maximum 29-fold) and VEGF (maximum 23-fold); these were reversed on return to normoxia. The secretion of IL-6, leptin, MIF and VEGF from the adipocytes was also stimulated by exposure to 1% O2. These results demonstrate that hypoxia induces extensive changes in human adipocytes in the expression and release of inflammation-related adipokines. Hypoxia may underlie the development of the inflammatory response in adipocytes, leading to obesity-associated diseases.
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