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      Lipids and cell death in yeast

      research-article
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      Fems Yeast Research
      Blackwell Publishing Ltd
      Lipids, cell death, aging, yeast, apoptosis, lipotoxicity

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          Abstract

          Understanding lipid-induced malfunction represents a major challenge of today's biomedical research. The connection of lipids to cellular and organ dysfunction, cell death, and disease (often referred to as lipotoxicity) is more complex than the sole lipotoxic effects of excess free fatty acids and requires genetically tractable model systems for mechanistic investigation. We herein summarize recent advances in the field of lipid-induced toxicity that employ the established model system for cell death and aging research of budding yeast Saccharomyces cerevisiae. Studies in yeast have shed light on various aspects of lipotoxicity, including free fatty acid toxicity, sphingolipid-modulated cell death as well as the involvement of cardiolipin and lipid peroxidation in the mitochondrial pathways of apoptosis. Regimens used range from exogenously applied lipids, genetic modulation of lipolysis and triacylglyceride synthesis, variations in sphingolipid/ceramide metabolism as well as changes in peroxisome function by either genetic or pharmacological means. In future, the yeast model of programmed cell death will further contribute to the clarification of crucial questions of lipid-associated malfunction.

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          FAT SIGNALS - Lipases and Lipolysis in Lipid Metabolism and Signaling

          Lipolysis is defined as the catabolism of triacylglycerols stored in cellular lipid droplets. Recent discoveries of essential lipolytic enzymes and characterization of numerous regulatory proteins and mechanisms have fundamentally changed our perception of lipolysis and its impact on cellular metabolism. New findings that lipolytic products and intermediates participate in cellular signaling processes and that “lipolytic signaling” is particularly important in many nonadipose tissues unveil a previously underappreciated aspect of lipolysis, which may be relevant for human disease.
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            Revitalizing membrane rafts: new tools and insights.

            Ten years ago, we wrote a Review on lipid rafts and signalling in the launch issue of Nature Reviews Molecular Cell Biology. At the time, this field was suffering from ambiguous methodology and imprecise nomenclature. Now, new techniques are deepening our insight into the dynamics of membrane organization. Here, we discuss how the field has matured and present an evolving model in which membranes are occupied by fluctuating nanoscale assemblies of sphingolipids, cholesterol and proteins that can be stabilized into platforms that are important in signalling, viral infection and membrane trafficking.
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              Many ceramides.

              Intensive research over the past 2 decades has implicated ceramide in the regulation of several cell responses. However, emerging evidence points to dramatic complexities in ceramide metabolism and structure that defy the prevailing unifying hypothesis on ceramide function that is based on the understanding of ceramide as a single entity. Here, we develop the concept that "ceramide" constitutes a family of closely related molecules, subject to metabolism by >28 enzymes and with >200 structurally distinct mammalian ceramides distinguished by specific structural modifications. These ceramides are synthesized in a combinatorial fashion with distinct enzymes responsible for the specific modifications. These multiple pathways of ceramide generation led to the hypothesis that individual ceramide molecular species are regulated by specific biochemical pathways in distinct subcellular compartments and execute distinct functions. In this minireview, we describe the "many ceramides" paradigm, along with the rationale, supporting evidence, and implications for our understanding of bioactive sphingolipids and approaches for unraveling these pathways.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                FEMS Yeast Res
                FEMS Yeast Res
                fyr
                Fems Yeast Research
                Blackwell Publishing Ltd (Oxford, UK )
                1567-1356
                1567-1364
                February 2014
                30 October 2013
                : 14
                : 1
                : 179-197
                Affiliations
                Institute of Molecular Biosciences, University of Graz Graz, Austria
                Author notes
                Tobias Eisenberg or Sabrina Büttner, Institute of Molecular Biosciences, Humboldtstr. 50, University of Graz, 8010 Graz, Austria. Tel.: +43 316 3801499; fax: +43 316 3809898; e-mail: tobias.eisenberg@ 123456uni-graz.at or sabrina.buettner@ 123456uni-graz.at
                Article
                10.1111/1567-1364.12105
                4255311
                24119111
                5c746f87-8c8a-4743-9e46-6f808762dcdb
                Copyright © 2014 Federation of European Microbiological Societies. Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 12 June 2013
                : 21 August 2013
                : 25 September 2013
                Categories
                Minireviews

                Molecular biology
                lipids,cell death,aging,yeast,apoptosis,lipotoxicity
                Molecular biology
                lipids, cell death, aging, yeast, apoptosis, lipotoxicity

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