Peroxisomes: A Nexus for Lipid Metabolism and Cellular Signaling

Slides:



Advertisements
Similar presentations
Figure, Head group attachment Membrane phospholipids:
Advertisements

Chapter 21 Biosynthetic Pathways
Fatty Acid Metabolism. Why are fatty acids important to cells? fuel molecules stored as triacylglycerols building blocks phospholipids glycolipids precursors.
Functions of mitochondrial ISCU and cytosolic ISCU in mammalian iron-sulfur cluster biogenesis and iron homeostasis Wing-Hang Tong, Tracey A. Rouault Cell.
If fatty acid synthesis occurs in the cytosol, where does the acetyl-CoA come from? Acetyl-CoA (not from fatty acid oxidation) is generated in the mitochondria.
Figure, Head group attachment Membrane phospholipids:
Chapter 21 Biosynthetic Pathways. Introduction In most living organisms, the pathways by which a compound is synthesized are usually different from the.
Pratt & Cornely, Chapter 17
KEY AREA 7: Cellular Respiration
Glycerophospholipids
Fatty acid synthesis (Lipogenesis & Lipolysis)
METABOLISM OF LIPIDS: SYNTHESIS OF FATTY ACIDS
FATTY ACID BIOSYNTHESIS
KEY CONCEPT Carbon-based molecules are the foundation of life.
FAT SIGNALS - Lipases and Lipolysis in Lipid Metabolism and Signaling
Metabolic Processes Metabolic reactions are of two types:
Peroxisomes: A Nexus for Lipid Metabolism and Cellular Signaling
Novel SIRT1 Mutation Linked to Autoimmune Diabetes in Humans
Lipid-Induced Mitochondrial Stress and Insulin Action in Muscle
ERRγ—A New Player in β Cell Maturation
“Corination” of the proANP converting enzyme
PPARα: Savior or savage?
Uncoupling proteins and non-alcoholic fatty liver disease
24.5 Fatty Acid Synthesis When the body has met all its energy needs and the glycogen stores are full, acetyl CoA from the breakdown of carbohydrates and.
Acetate Fuels the Cancer Engine
Lipids.
Figure 3 Biosynthetic pathway of plasmalogens
Fingered for a Fat Fate Cell Metabolism
Things with Carbon and Hydrogen!
Endothelial Cells Get β-ox-ed In to Support Lymphangiogenesis
Coming up for air: HIF-1 and mitochondrial oxygen consumption
SERCA2b Cycles Its Way to UCP1-Independent Thermogenesis in Beige Fat
Metformin: From Mechanisms of Action to Therapies
Peroxisome By: Ismael & taichiro.
Adiponectin, Leptin, and Fatty Acids in the Maintenance of Metabolic Homeostasis through Adipose Tissue Crosstalk  Jennifer H. Stern, Joseph M. Rutkowski,
Guido T. Bommer, Ormond A. MacDougald  Cell Metabolism 
Martin D. Brand, Telma C. Esteves  Cell Metabolism 
ACSF3 and Mal(onate)-Adapted Mitochondria
Why We Should Put Clothes on Mice
Autophagy: A Sweet Process in Diabetes
Metabolomics and Metabolic Diseases: Where Do We Stand?
Ng Shyh-Chang, George Q. Daley  Cell Metabolism 
Cristoforo Silvestri, Vincenzo Di Marzo  Cell Metabolism 
Autophagy: A Potential Link between Obesity and Insulin Resistance
Volume 16, Issue 2, Pages (August 2012)
Lipid droplets Current Biology
Volume 17, Issue 5, Pages (May 2013)
Obesity and the Regulation of Energy Balance
An Emerging Role of mTOR in Lipid Biosynthesis
Daniel J. Rader, Ellen Puré  Cell Metabolism 
Figure 5 Ether-containing lipid biosynthesis pathways
Metabolic Control of Chloroplast Gene Expression: An Emerging Theme
Mitochondria in the Regulation of Innate and Adaptive Immunity
Sizing up Surfactant Synthesis
Figure 1 Glycerophospholipid classes and subclasses
Conserved Metabolic Regulatory Functions of Sirtuins
Modulating Cholesterol Homeostasis to Build a Better T Cell
Carbohydrate response element binding protein, ChREBP, a transcription factor coupling hepatic glucose utilization and lipid synthesis  Kosaku Uyeda,
Daniel J. Rader, Ellen Puré  Cell Metabolism 
Glycogen Synthase: An Old Enzyme with a New Trick
Volume 11, Issue 5, Pages (November 2012)
AMPK: An Emerging Drug Target for Diabetes and the Metabolic Syndrome
Carbohydrate response element binding protein, ChREBP, a transcription factor coupling hepatic glucose utilization and lipid synthesis  Kosaku Uyeda,
Jun-Young Seo, Rakina Yaneva, Peter Cresswell  Cell Host & Microbe 
Lipid Metabolism Greases the Stem Cell Engine
FAT SIGNALS - Lipases and Lipolysis in Lipid Metabolism and Signaling
Peroxisome Biogenesis: End of the Debate
The Long and Short of Fatty Acid Synthesis
C16:0-Ceramide Signals Insulin Resistance
Presentation transcript:

Peroxisomes: A Nexus for Lipid Metabolism and Cellular Signaling Irfan J. Lodhi, Clay F. Semenkovich  Cell Metabolism  Volume 19, Issue 3, Pages 380-392 (March 2014) DOI: 10.1016/j.cmet.2014.01.002 Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 1 Structure and Functions of Peroxisomes The peroxisome is a single membrane-enclosed organelle that plays an important role in metabolism. The main metabolic functions of peroxisomes in mammalian cells include β-oxidation of very long chain fatty acids, α-oxidation of branched chain fatty acids, synthesis of bile acids and ether-linked phospholipids, and removal of reactive oxygen species. Peroxisomes in many, but not all, cell types contain a dense crystalline core of oxidative enzymes. Cell Metabolism 2014 19, 380-392DOI: (10.1016/j.cmet.2014.01.002) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 2 Potential Pathways to Peroxisomal Biogenesis (A) Peroxisomes are generated autonomously through division of preexisting organelles (top) or through a de novo process involving budding from the ER followed by import of matrix proteins (bottom). (B) Peroxisomal membrane protein import. Peroxisomal membrane proteins (PMPs) are imported posttranslationally to the peroxisomal membrane. Pex19 is a soluble chaperone that binds to PMPs and transports them to the peroxisomal membrane, where it docks with a complex containing Pex16 and Pex3. Following insertion of the PMP, Pex19 is recycled back to the cytosol. Cell Metabolism 2014 19, 380-392DOI: (10.1016/j.cmet.2014.01.002) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 3 Chemical Structures of Diacyl- and Ether-Linked Phospholipids In conventional diacyl phospholipids, fatty acyl side chains are linked to the sn-1 and sn-2 positions of the glycerol backbone by ester bonds. Ether-linked phospholipids are a special class of glycerophospholipids that have an alkyl chain attached to the sn-1 position by an ether bond. The sn-2 substituent of ether lipids is generally an ester-linked acyl chain as in diacylphospholipids. The head group of ether phospholipids is usually choline or ethanolamine. Some of the ether linked phospholipids have a cis double bond adjacent to the ether bond and are referred to as alkenyl-acylphospholipids, or more commonly as plasmalogens. According to convention, plasmalogen form of phospholipids have the prefix “plasmenyl,” as in plasmenylcholine. Alkyl-acylphospholipids have the prefix “plasmanyl.” Cell Metabolism 2014 19, 380-392DOI: (10.1016/j.cmet.2014.01.002) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 4 Acyl DHAP Pathway of Phospholipid Synthesis This pathway is obligatory for synthesis of ether-linked phospholipids and is also an alternative route for synthesis of diacylphospholipids. Phospholipid synthesis begins in peroxisomes and is completed in the ER. The pathway uses dihydroxacetone phosphate (DHAP), generated by glycerol 3-phosphate dehydrogenase (G3PDH)-mediated dehydrogenation of G3P, as a building block for the synthesis of phospholipids. Fatty acyl CoA produced by de novo lipogenesis is used by DHAPAT (DHAP acyltransferase) to acylate DHAP or is reduced to a fatty alcohol by a peroxisomal membrane-associated fatty acyl CoA reductase in an NADPH-dependent reaction. The fatty alcohol is used by alkyl DHAP synthase (ADHAPS) to convert acyl DHAP to alkyl DHAP. Acyl DHAP or alkyl DHAP can be reduced to 1-acyl G3P (lysophosphatidic acid) or its ether lipid equivalent, 1-O-alkyl G3P (AGP), respectively, by acyl/alkyl DHAP reductase (also called PexRAP). The subsequent steps of phospholipid synthesis, including acylation at the sn-2 position, occur in the ER. Cell Metabolism 2014 19, 380-392DOI: (10.1016/j.cmet.2014.01.002) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 5 Relationship between Peroxisomes and PPARγ PPARγ is a key regulator of adipocyte differentiation as well as function and is activated by multiple endogenous ligands, including alkyl ether phospholipids, which are synthesized in peroxisomes. PPARγ exists as a heterodimer with RXR and regulates expression of a large number of genes harboring PPAR response elements (PPRE), including genes involved in adipogenesis, lipid metabolism, and glucose homeostasis. Emerging studies indicate that PPARγ also regulates the expression of genes involved in peroxisomal biogenesis, suggesting a feed-forward mechanism of PPARγ activation. Cell Metabolism 2014 19, 380-392DOI: (10.1016/j.cmet.2014.01.002) Copyright © 2014 Elsevier Inc. Terms and Conditions