Staff Publications

Staff Publications

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    'Staff publications' is the digital repository of Wageningen University & Research

    'Staff publications' contains references to publications authored by Wageningen University staff from 1976 onward.

    Publications authored by the staff of the Research Institutes are available from 1995 onwards.

    Full text documents are added when available. The database is updated daily and currently holds about 240,000 items, of which 72,000 in open access.

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Record number 429435
Title Plasma mannose-binding lectin is stimulated by PPARa in humans
Author(s) Rakhshandehroo, M.; Stienstra, R.; Wit, N.J.W. de; Bragt, M.C.E.; Haluzik, M.; Mensink, R.P.; Muller, M.R.; Kersten, A.H.
Source American Journal of Physiology. Endocrinology and Metabolism 302 (2012)5. - ISSN 0193-1849 - p. E595 - E602.
DOI http://dx.doi.org/10.1152/ajpendo.00299.2011
Department(s) Chair Nutrition Metabolism and Genomics
VLAG
Publication type Refereed Article in a scientific journal
Publication year 2012
Keyword(s) proliferator-activated receptors - hepatic lipid-metabolism - fatty liver-disease - fasting response - mouse - gene - fibroblast-growth-factor-21 - inflammation - fenofibrate - regulator
Abstract The peroxisome proliferator activated receptor-a (PPARa) is a major transcriptional regulator of lipid metabolism in liver and represents the molecular target for hypolipidemic fibrate drugs. Effects of PPARa on lipid metabolism are partially mediated by circulating proteins such as FGF21 and ANGPTL4. The present study was undertaken to screen for and identify circulating proteins produced by human liver that are under the control of PPARa. Toward that aim, primary human hepatocytes were treated with the synthetic PPARa agonist Wy-14643 and whole genome expression data selected for secreted proteins. Expression of FGF21, ANGPTL4, and mannose-binding lectin (MBL), a soluble mediator of innate immunity and primary component of the lectin branch of the complement system, was markedly upregulated by Wy-14643 in primary human hepatocytes. Mice express two MBL isomers, Mbl1 and Mbl2. Mbl1 mRNA was weakly induced by Wy-14643 in primary mouse hepatocytes and remained unaltered by Wy-14643 in mouse liver. Mbl2 mRNA was unchanged by Wy-14643 in primary mouse hepatocytes and was strongly reduced by Wy-14643 in mouse liver. Remarkably, plasma Mbl1 levels were increased by chronic PPARa activation in lean and obese mice. Importantly, in two independent clinical trials, treatment with the PPARa agonist fenofibrate at 200 mg/day for 6 wk and 3 mo increased plasma MBL levels by 73 (P = 0.0016) and 86% (P = 0.017), respectively. It is concluded that hepatocyte gene expression and plasma levels of MBL are stimulated by PPARa and fenofibrate in humans, linking PPARa to regulation of innate immunity and complement activation in humans and suggesting a possible role of MBL in lipid metabolism.
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