Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101676
Title: The peroxisomal enzyme L-PBE is required to prevent the dietary toxicity of medium-chain Fatty acids
Authors: Reddy, Janardan K.
Ding, Jun
Loizides-Mangold, Ursula
Rando, Gianpaolo
Zoete, Vincent
Michielin, Olivier
Wahli, Walter
Riezman, Howard
Thorens, Bernard
Keywords: DRNTU::Science::Medicine
Issue Date: 2013
Source: Ding, J., Loizides-Mangold, U., Rando, G., Zoete, V., Michielin, O., Reddy, J. K., et al. (2013). The peroxisomal enzyme L-PBE is required to prevent the dietary toxicity of medium-chain Fatty acids. Cell reports, 5(1), 248-258.
Series/Report no.: Cell reports
Abstract: Specific metabolic pathways are activated by different nutrients to adapt the organism to available resources. Although essential, these mechanisms are incompletely defined. Here, we report that medium-chain fatty acids contained in coconut oil, a major source of dietary fat, induce the liver ω-oxidation genes Cyp4a10 and Cyp4a14 to increase the production of dicarboxylic fatty acids. Furthermore, these activate all ω- and β-oxidation pathways through peroxisome proliferator activated receptor (PPAR) α and PPARγ, an activation loop normally kept under control by dicarboxylic fatty acid degradation by the peroxisomal enzyme L-PBE. Indeed, L-pbe−/− mice fed coconut oil overaccumulate dicarboxylic fatty acids, which activate all fatty acid oxidation pathways and lead to liver inflammation, fibrosis, and death. Thus, the correct homeostasis of dicarboxylic fatty acids is a means to regulate the efficient utilization of ingested medium-chain fatty acids, and its deregulation exemplifies the intricate relationship between impaired metabolism and inflammation.
URI: https://hdl.handle.net/10356/101676
http://hdl.handle.net/10220/18745
ISSN: 2211-1247
DOI: 10.1016/j.celrep.2013.08.032
Rights: © 2013 The Authors. This paper was published in Cell Reports and is made available as an electronic reprint (preprint) with permission of The Authors. The paper can be found at the following official DOI: [http://dx.doi.org/10.1016/j.celrep.2013.08.032].  One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:LKCMedicine Journal Articles

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