The PNPLA family of enzymes: characterisation and biological role

Abstract This paper brings a brief review of the human patatin-like phospholipase domain-containing protein (PNPLA) family. Even though it consists of only nine members, their physiological roles and mechanisms of their catalytic activity are not fully understood. However, the results of a number of knock-out and gain- or loss-of-function research models suggest that these enzymes have an important role in maintaining the homeostasis and integrity of organelle membranes, in cell growth, signalling, cell death, and the metabolism of lipids such as triacylglycerol, phospholipids, ceramides, and retinyl esters. Research has also revealed a connection between PNPLA family member mutations or irregular catalytic activity and the development of various diseases. Here we summarise important findings published so far and discuss their structure, localisation in the cell, distribution in the tissues, specificity for substrates, and their potential physiological role, especially in view of their potential as drug targets.

[1]  S. Pirkmajer,et al.  Insulin, dibutyryl-cAMP, and glucose modulate expression of patatin-like domain containing protein 7 in cultured human myotubes , 2023, Frontiers in Endocrinology.

[2]  H. Kiyonari,et al.  Hepatic phosphatidylcholine catabolism driven by PNPLA7 and PNPLA8 supplies endogenous choline to replenish the methionine cycle with methyl groups. , 2023, Cell reports.

[3]  D. Schuppan,et al.  PNPLA3(I148M) Inhibits Lipolysis by Perilipin-5-Dependent Competition with ATGL , 2022, Cells.

[4]  E. Liu,et al.  Lipid-laden lung mesenchymal cells foster breast cancer metastasis via metabolic reprogramming of tumor cells and natural killer cells. , 2022, Cell metabolism.

[5]  A. Saghatelian,et al.  ATGL is a biosynthetic enzyme for fatty acid esters of hydroxy fatty acids , 2022, Nature.

[6]  K. Smolková,et al.  Antioxidant Role and Cardiolipin Remodeling by Redox-Activated Mitochondrial Ca2+-Independent Phospholipase A2γ in the Brain , 2022, Antioxidants.

[7]  V. Mlitz,et al.  Hepatocyte‐specific deletion of adipose triglyceride lipase (adipose triglyceride lipase/patatin‐like phospholipase domain containing 2) ameliorates dietary induced steatohepatitis in mice , 2021 .

[8]  C. Chalfant,et al.  Alterations in β-Cell Sphingolipid Profile Associated with ER Stress and iPLA2β: Another Contributor to β-Cell Apoptosis in Type 1 Diabetes , 2021, Molecules.

[9]  R. Owens,et al.  Optimized expression and purification of adipose triglyceride lipase improved hydrolytic and transacylation activities in vitro , 2021, The Journal of biological chemistry.

[10]  D. Powell,et al.  Histopathology is required to identify and characterize myopathies in high-throughput phenotype screening of genetically engineered mice , 2021, Veterinary pathology.

[11]  B. Stockwell,et al.  iPLA2β-mediated lipid detoxification controls p53-driven ferroptosis independent of GPX4 , 2021, Nature Communications.

[12]  G. Fu,et al.  iPLA2β Contributes to ER Stress-Induced Apoptosis during Myocardial Ischemia/Reperfusion Injury , 2021, Cells.

[13]  Zhaofan Luo,et al.  Adipose triglyceride lipase promotes the proliferation of colorectal cancer cells via enhancing the lipolytic pathway , 2021, Journal of cellular and molecular medicine.

[14]  B. Dilthey,et al.  High-fat diet activates liver iPLA2γ generating eicosanoids that mediate metabolic stress , 2021, Journal of lipid research.

[15]  Shaoyun Wang,et al.  Patatin primary structural properties and effects on lipid metabolism. , 2020, Food chemistry.

[16]  M. Murakami,et al.  Updating Phospholipase A2 Biology , 2020, Biomolecules.

[17]  Haowei Song,et al.  Metabolic Effects of Selective Deletion of Group VIA Phospholipase A2 from Macrophages or Pancreatic Islet Beta-Cells , 2020, Biomolecules.

[18]  X. Zhang,et al.  Lung mesenchymal cells elicit lipid storage in neutrophils that fuel breast cancer lung metastasis , 2020, Nature immunology.

[19]  R. Zechner,et al.  Adipose triglyceride lipase activity regulates cancer cell proliferation via AMP-kinase and mTOR signaling , 2020, Biochimica et biophysica acta. Molecular and cell biology of lipids.

[20]  C. Heier,et al.  Interaction of the Lysophospholipase PNPLA7 with Lipid Droplets through the Catalytic Region , 2020, Molecules and cells.

[21]  Alexander Yang,et al.  Adipocyte lipolysis: from molecular mechanisms of regulation to disease and therapeutics. , 2020, The Biochemical journal.

[22]  B. Dilthey,et al.  12-LOX catalyzes the oxidation of 2-arachidonoyl-lysolipids in platelets generating eicosanoid-lysolipids that are attenuated by iPLA2γ knockout , 2020, The Journal of Biological Chemistry.

[23]  Sanjeeva J. Wijeyesakere,et al.  Neuropathy target esterase (NTE/PNPLA6) and organophosphorus compound-induced delayed neurotoxicity (OPIDN) , 2020, Advances in Neurotoxicology.

[24]  Ji-zheng Chen,et al.  The Patatin‐Like Phospholipase Domain Containing Protein 7 Facilitates VLDL Secretion by Modulating ApoE Stability , 2020, Hepatology.

[25]  M. Oberer,et al.  Protein-protein interactions regulate the activity of Adipose Triglyceride Lipase in intracellular lipolysis. , 2020, Biochimie.

[26]  X. Dong PNPLA3—A Potential Therapeutic Target for Personalized Treatment of Chronic Liver Disease , 2019, Front. Med..

[27]  Hongxia Liu,et al.  PNPLA3 I148M mediates the regulatory effect of NF‐kB on inflammation in PA‐treated HepG2 cells , 2019, Journal of cellular and molecular medicine.

[28]  C. Heier,et al.  Characterization of the Interaction of Neuropathy Target Esterase with the Endoplasmic Reticulum and Lipid Droplets , 2019, Biomolecules.

[29]  Kang Wang,et al.  ATGL promotes the proliferation of hepatocellular carcinoma cells via the p‐AKT signaling pathway , 2019, Journal of biochemical and molecular toxicology.

[30]  Alexander J. Nelson,et al.  iPLA2β and its role in male fertility, neurological disorders, metabolic disorders, and inflammation. , 2019, Biochimica et biophysica acta. Molecular and cell biology of lipids.

[31]  J. Balsinde,et al.  Selectivity of phospholipid hydrolysis by phospholipase A2 enzymes in activated cells leading to polyunsaturated fatty acid mobilization. , 2019, Biochimica et biophysica acta. Molecular and cell biology of lipids.

[32]  S. Romeo,et al.  The role of PNPLA3 in health and disease. , 2019, Biochimica et biophysica acta. Molecular and cell biology of lipids.

[33]  M. Schweiger,et al.  Of mice and men: The physiological role of adipose triglyceride lipase (ATGL)☆ , 2019, Biochimica et biophysica acta. Molecular and cell biology of lipids.

[34]  Hyeon-Cheol Lee,et al.  Lipid-metabolizing serine hydrolases in the mammalian central nervous system: endocannabinoids and beyond. , 2019, Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids.

[35]  N. Davidson,et al.  Missense Mutant Patatin‐Like Phospholipase Domain Containing 3 Alters Lipid Droplet Turnover in Partnership With CGI‐58 , 2019, Hepatology.

[36]  Jonathan C. Cohen,et al.  Accumulation of PNPLA3 on lipid droplets is the basis of associated hepatic steatosis , 2019, Proceedings of the National Academy of Sciences.

[37]  J. Granneman,et al.  Dynamic interactions of ABHD5 with PNPLA3 regulate triacylglycerol metabolism in brown adipocytes , 2019, Nature Metabolism.

[38]  Jonathan C. Cohen,et al.  PNPLA3, CGI‐58, and Inhibition of Hepatic Triglyceride Hydrolysis in Mice , 2019, Hepatology.

[39]  A. Kihara,et al.  Molecular mechanism of the ichthyosis pathology of Chanarin-Dorfman syndrome: Stimulation of PNPLA1-catalyzed ω-O-acylceramide production by ABHD5. , 2018, Journal of dermatological science.

[40]  Kei Yamamoto,et al.  Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics , 2018, Inflammation and regeneration.

[41]  Jun Ren,et al.  Autophagy as an emerging target in cardiorenal metabolic disease: From pathophysiology to management , 2018, Pharmacology & therapeutics.

[42]  G. Haemmerle,et al.  ABHD5 stimulates PNPLA1-mediated ω-O-acylceramide biosynthesis essential for a functional skin permeability barrier[S] , 2018, Journal of Lipid Research.

[43]  H. Bellen,et al.  Phospholipase PLA2G6, a Parkinsonism-Associated Gene, Affects Vps26 and Vps35, Retromer Function, and Ceramide Levels, Similar to α-Synuclein Gain. , 2018, Cell metabolism.

[44]  Ying-Zu Huang,et al.  PARK14 (D331Y) PLA2G6 Causes Early-Onset Degeneration of Substantia Nigra Dopaminergic Neurons by Inducing Mitochondrial Dysfunction, ER Stress, Mitophagy Impairment and Transcriptional Dysregulation in a Knockin Mouse Model , 2018, Molecular Neurobiology.

[45]  Bo Zhang,et al.  Long non-coding RNA NEAT1-modulated abnormal lipolysis via ATGL drives hepatocellular carcinoma proliferation , 2018, Molecular Cancer.

[46]  G. Mirzaa,et al.  A neurodegenerative mitochondrial disease phenotype due to biallelic loss‐of‐function variants in PNPLA8 encoding calcium‐independent phospholipase A2γ , 2018, American journal of medical genetics. Part A.

[47]  R. Gross,et al.  The structure of iPLA2β reveals dimeric active sites and suggests mechanisms of regulation and localization , 2018, Nature Communications.

[48]  Ning Liu,et al.  Lowered iPLA2γ activity causes increased mitochondrial lipid peroxidation and mitochondrial dysfunction in a rotenone-induced model of Parkinson's disease , 2018, Experimental Neurology.

[49]  Kui Yang,et al.  Heart failure–induced activation of phospholipase iPLA2γ generates hydroxyeicosatetraenoic acids opening the mitochondrial permeability transition pore , 2017, The Journal of Biological Chemistry.

[50]  Luca Valenti,et al.  Mutant PNPLA3 I148M protein as pharmacological target for liver disease , 2017, Hepatology.

[51]  R. Zechner,et al.  The phospholipase PNPLA7 functions as a lysophosphatidylcholine hydrolase and interacts with lipid droplets through its catalytic domain , 2017, The Journal of Biological Chemistry.

[52]  Jonathan C. Cohen,et al.  The PNPLA3 variant associated with fatty liver disease (I148M) accumulates on lipid droplets by evading ubiquitylation , 2017, Hepatology.

[53]  C. Diwoky,et al.  Pharmacological inhibition of adipose triglyceride lipase corrects high-fat diet-induced insulin resistance and hepatosteatosis in mice , 2017, Nature Communications.

[54]  M. Murakami,et al.  PNPLA1 has a crucial role in skin barrier function by directing acylceramide biosynthesis , 2017, Nature Communications.

[55]  A. Kihara,et al.  PNPLA1 is a transacylase essential for the generation of the skin barrier lipid ω-O-acylceramide , 2017, Nature Communications.

[56]  M. Sogorb,et al.  Roles of NTE protein and encoding gene in development and neurodevelopmental toxicity. , 2016, Chemico-biological interactions.

[57]  T. Osborne,et al.  SREBP-2/PNPLA8 axis improves non-alcoholic fatty liver disease through activation of autophagy , 2016, Scientific Reports.

[58]  Ping-An Chang,et al.  Identification mouse patatin-like phospholipase domain containing protein 1 as a skin-specific and membrane-associated protein. , 2016, Gene.

[59]  M. Czaja,et al.  Regulation and Functions of Autophagic Lipolysis , 2016, Trends in Endocrinology & Metabolism.

[60]  R. Zechner,et al.  PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides. , 2016, The Journal of investigative dermatology.

[61]  G. Schmitz,et al.  iPLA2β deficiency attenuates obesity and hepatic steatosis in ob/ob mice through hepatic fatty-acyl phospholipid remodeling. , 2016, Biochimica et biophysica acta.

[62]  Elsje G. Otten,et al.  Autophagy, lipophagy and lysosomal lipid storage disorders. , 2016, Biochimica et biophysica acta.

[63]  M. L. Greenberg,et al.  Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function , 2016, Journal of Bioenergetics and Biomembranes.

[64]  X. Lei,et al.  Calcium-independent phospholipases A2 and their roles in biological processes and diseases , 2015, Journal of Lipid Research.

[65]  D. Pfeiffer,et al.  The iPLA2γ is identified as the membrane potential sensitive phospholipase in liver mitochondria , 2015, FEBS letters.

[66]  R. Zechner,et al.  Adipose triglyceride lipase is involved in the mobilization of triglyceride and retinoid stores of hepatic stellate cells , 2015, Biochimica et biophysica acta.

[67]  Laurie D. Smith,et al.  Loss of Function Variants in Human PNPLA8 Encoding Calcium‐Independent Phospholipase A2γ Recapitulate the Mitochondriopathy of the Homologous Null Mouse , 2015, Human mutation.

[68]  M. Sogorb,et al.  Silencing of PNPLA6, the neuropathy target esterase (NTE) codifying gene, alters neurodifferentiation of human embryonal carcinoma stem cells (NT2) , 2014, Neuroscience.

[69]  J. Stuckey,et al.  Crystal Structure of Patatin-17 in Complex with Aged and Non-Aged Organophosphorus Compounds , 2014, PloS one.

[70]  D. Pfeiffer,et al.  Regulation of the Ca2-independent phospholipase A2 in liver mitochondria by changes in the energetic state , 2014, Journal of Lipid Research.

[71]  K. Stenkula,et al.  Adiponutrin: a multimeric plasma protein. , 2014, Biochemical and biophysical research communications.

[72]  R. Zechner,et al.  Adipose triglyceride lipase activity is inhibited by long-chain acyl-coenzyme A , 2014, Biochimica et biophysica acta.

[73]  T. Proikas-Cezanne,et al.  Neutral Lipid Stores and Lipase PNPLA5 Contribute to Autophagosome Biogenesis , 2014, Current Biology.

[74]  Yi-Jun Wu,et al.  Identification of human patatin-like phospholipase domain-containing protein 1 and a mutant in human cervical cancer HeLa cells , 2013, Molecular Biology Reports.

[75]  Sricharan Murugesan,et al.  Identification of Diverse Lipid Droplet Targeting Motifs in the PNPLA Family of Triglyceride Lipases , 2013, PloS one.

[76]  R. Parton,et al.  PNPLA3/adiponutrin functions in lipid droplet formation , 2013, Biology of the cell.

[77]  Sanjeeva J. Wijeyesakere,et al.  Neuropathy target esterase (NTE): overview and future. , 2013, Chemico-biological interactions.

[78]  C. Townsend,et al.  Intrinsic evolutionary constraints on protease structure, enzyme acylation, and the identity of the catalytic triad , 2012, Proceedings of the National Academy of Sciences.

[79]  Virgil L. Woods,et al.  Fluoroketone Inhibition of Ca2+-Independent Phospholipase A2 through Binding Pocket Association Defined by Hydrogen/Deuterium Exchange and Molecular Dynamics , 2012, Journal of the American Chemical Society.

[80]  Robert V Farese,et al.  Studies on the Substrate and Stereo/Regioselectivity of Adipose Triglyceride Lipase, Hormone-sensitive Lipase, and Diacylglycerol-O-acyltransferases* , 2012, The Journal of Biological Chemistry.

[81]  A. Audhya,et al.  Roles of Acidic Phospholipids and Nucleotides in Regulating Membrane Binding and Activity of a Calcium-independent Phospholipase A2 Isoform* , 2012, The Journal of Biological Chemistry.

[82]  S. Rapoport,et al.  Disturbed brain phospholipid and docosahexaenoic acid metabolism in calcium-independent phospholipase A(2)-VIA (iPLA(2)β)-knockout mice. , 2012, Biochimica et biophysica acta.

[83]  R. Gross,et al.  Genetic Ablation of Calcium-independent Phospholipase A2γ (iPLA2γ) Attenuates Calcium-induced Opening of the Mitochondrial Permeability Transition Pore and Resultant Cytochrome c Release* , 2012, The Journal of Biological Chemistry.

[84]  Robert V Farese,et al.  Lipid droplets and cellular lipid metabolism. , 2012, Annual review of biochemistry.

[85]  Sarah A. Scott,et al.  Adiponutrin functions as a nutritionally regulated lysophosphatidic acid acyltransferase. , 2012, Cell metabolism.

[86]  R. Holmes Vertebrate patatin-like phospholipase domain-containing protein 4 (PNPLA4) genes and proteins: a gene with a role in retinol metabolism , 2012, 3 Biotech.

[87]  R. Holmes Comparative studies of adipose triglyceride lipase genes and proteins: an ancient gene in vertebrate evolution , 2012 .

[88]  Guenter Haemmerle,et al.  FAT SIGNALS - Lipases and Lipolysis in Lipid Metabolism and Signaling , 2012, Cell metabolism.

[89]  R. Gross,et al.  Activation of Mitochondrial Calcium-independent Phospholipase A2γ (iPLA2γ) by Divalent Cations Mediating Arachidonate Release and Production of Downstream Eicosanoids*♦ , 2012, The Journal of Biological Chemistry.

[90]  Ping-An Chang,et al.  Degradation of mouse NTE-related esterase by macroautophagy and the proteasome , 2012, Molecular Biology Reports.

[91]  F. Galibert,et al.  PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans , 2012, Nature Genetics.

[92]  U. Taschler,et al.  Retinyl ester hydrolases and their roles in vitamin A homeostasis , 2012, Biochimica et biophysica acta.

[93]  R. Zechner,et al.  The Minimal Domain of Adipose Triglyceride Lipase (ATGL) Ranges until Leucine 254 and Can Be Activated and Inhibited by CGI-58 and G0S2, Respectively , 2011, PloS one.

[94]  E. Dennis,et al.  Phospholipase A2 enzymes: physical structure, biological function, disease implication, chemical inhibition, and therapeutic intervention. , 2011, Chemical reviews.

[95]  Y. Miki,et al.  Recent progress in phospholipase A₂ research: from cells to animals to humans. , 2011, Progress in lipid research.

[96]  R. Zechner,et al.  Lipolysis – A highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores , 2011, Progress in lipid research.

[97]  J. Granneman,et al.  Interactions of Perilipin-5 (Plin5) with Adipose Triglyceride Lipase* , 2010, The Journal of Biological Chemistry.

[98]  Yi-Jun Wu,et al.  Regulation of neuropathy target esterase by the cAMP/protein kinase A signal. , 2010, Pharmacological research.

[99]  Haowei Song,et al.  Effects of Endoplasmic Reticulum Stress on Group VIA Phospholipase A2 in Beta Cells Include Tyrosine Phosphorylation and Increased Association with Calnexin* , 2010, The Journal of Biological Chemistry.

[100]  R. Worden,et al.  Influence of lysophospholipid hydrolysis by the catalytic domain of neuropathy target esterase on the fluidity of bilayer lipid membranes. , 2010, Biochimica et biophysica acta.

[101]  J. Stuckey,et al.  Constructs of human neuropathy target esterase catalytic domain containing mutations related to motor neuron disease have altered enzymatic properties. , 2010, Toxicology letters.

[102]  Yi-Jun Wu,et al.  Neuropathy target esterase: an essential enzyme for neural development and axonal maintenance. , 2010, The international journal of biochemistry & cell biology.

[103]  Xianlin Han,et al.  Genetic Ablation of Calcium-independent Phospholipase A2γ Leads to Alterations in Hippocampal Cardiolipin Content and Molecular Species Distribution, Mitochondrial Degeneration, Autophagy, and Cognitive Dysfunction* , 2009, The Journal of Biological Chemistry.

[104]  Petra C. Kienesberger,et al.  Adipose Triglyceride Lipase Deficiency Causes Tissue-specific Changes in Insulin Signaling* , 2009, The Journal of Biological Chemistry.

[105]  R. Zechner,et al.  Neutral lipid storage disease: genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or CGI-58/ABHD5. , 2009, American journal of physiology. Endocrinology and metabolism.

[106]  R. Zechner,et al.  Fate of fat: the role of adipose triglyceride lipase in lipolysis. , 2009, Biochimica et biophysica acta.

[107]  M. Simon,et al.  GS2 as a retinol transacylase and as a catalytic dyad independent regulator of retinylester accretion. , 2009, Molecular genetics and metabolism.

[108]  R. Gross,et al.  Eicosanoid signalling pathways in the heart. , 2008, Cardiovascular research.

[109]  E. Bertini,et al.  Neurodegeneration associated with genetic defects in phospholipase A2 , 2008, Neurology.

[110]  S. Kohlwein,et al.  Identification of an Insulin-regulated Lysophospholipase with Homology to Neuropathy Target Esterase* , 2008, Journal of Biological Chemistry.

[111]  R. Schmidt,et al.  Molecular Pathogenesis of Genetic and Inherited Diseases Disrupted Membrane Homeostasis and Accumulation of Ubiquitinated Proteins in a Mouse Model of Infantile Neuroaxonal Dystrophy Caused by PLA 2 G 6 Mutations , 2010 .

[112]  L. Philipson,et al.  Glucose homeostasis, insulin secretion, and islet phospholipids in mice that overexpress iPLA2β in pancreatic β-cells and in iPLA2β-null mice , 2008 .

[113]  Alexander Wlodawer,et al.  The expanding diversity of serine hydrolases. , 2007, Current opinion in structural biology.

[114]  Yi-Jun Wu,et al.  Molecular cloning and expression of the C-terminal domain of mouse NTE-related esterase , 2007, Molecular and Cellular Biochemistry.

[115]  J. Stuckey,et al.  Modeling the Tertiary Structure of the Patatin Domain of Neuropathy Target Esterase , 2007, The protein journal.

[116]  S. Commans,et al.  Characterization of the human patatin-like phospholipase familys⃞ Published, JLR Papers in Press, June 25, 2006. , 2006, Journal of Lipid Research.

[117]  M. Simon,et al.  Molecular screening for GS2 lipase regulators: inhibition of keratinocyte retinylester hydrolysis by TIP47. , 2006, The Journal of investigative dermatology.

[118]  Sun Tian,et al.  Application of a sensitive collection heuristic for very large protein families: Evolutionary relationship between adipose triglyceride lipase (ATGL) and classic mammalian lipases , 2006, BMC Bioinformatics.

[119]  K. Makarova,et al.  ATGL has a key role in lipid droplet/adiposome degradation in mammalian cells , 2006, EMBO reports.

[120]  Xianlin Han,et al.  The Highly Selective Production of 2-Arachidonoyl Lysophosphatidylcholine Catalyzed by Purified Calcium-independent Phospholipase A2γ , 2005, Journal of Biological Chemistry.

[121]  Jay G Gao,et al.  Identification of a novel keratinocyte retinyl ester hydrolase as a transacylase and lipase. , 2005, The Journal of investigative dermatology.

[122]  R. Gross,et al.  Identification, Cloning, Expression, and Purification of Three Novel Human Calcium-independent Phospholipase A2 Family Members Possessing Triacylglycerol Lipase and Acylglycerol Transacylase Activities* , 2004, Journal of Biological Chemistry.

[123]  H. Sumimoto,et al.  Catalytic residues of group VIB calcium-independent phospholipase A2 (iPLA2gamma). , 2004, Biochemical and biophysical research communications.

[124]  W. Stallings,et al.  The crystal structure, mutagenesis, and activity studies reveal that patatin is a lipid acyl hydrolase with a Ser-Asp catalytic dyad. , 2003, Biochemistry.

[125]  H. Tanaka,et al.  A novel intracellular membrane-bound calcium-independent phospholipase A(2). , 2000, Biochemical and biophysical research communications.

[126]  R. Gross,et al.  The Genomic Organization, Complete mRNA Sequence, Cloning, and Expression of a Novel Human Intracellular Membrane-associated Calcium-independent Phospholipase A2 * , 2000, The Journal of Biological Chemistry.

[127]  A. Kossiakoff,et al.  Direct determination of the protonation states of aspartic acid-102 and histidine-57 in the tetrahedral intermediate of the serine proteases: neutron structure of trypsin. , 1981, Biochemistry.

[128]  iPLA 2 β Contributes to ER Stress ‐ Induced Apoptosis during Myocardial Ischemia / Reperfusion Injury , 2021 .

[129]  D. Gozuacik,et al.  Impairment of lipophagy by PNPLA1 mutations causes lipid droplet accumulation in primary fibroblasts of Autosomal Recessive Congenital Ichthyosis patients. , 2019, Journal of dermatological science.

[130]  Yang Liu,et al.  PNPLA5-knockout rats induced by CRISPR/Cas9 exhibit abnormal bleeding and lipid level , 2017 .

[131]  S. Pirkmajer,et al.  The Effects of Organophosphates in the Early Stages of Human Muscle Regeneration , 2015 .

[132]  T. Strom,et al.  PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum. , 2014, Brain : a journal of neurology.

[133]  Shenmin Zhang,et al.  Evidence for Proteolytic Processing and Stimulated Organelle Redistribution of iPLA2β , 2010 .

[134]  J. Flier,et al.  Adipose triglyceride lipase: function, regulation by insulin, and comparison with adiponutrin. , 2006, Diabetes.