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Lipid droplet proteins and metabolic diseases
Authors:Shimeng Xu  Xuelin Zhang  Pingsheng Liu
Affiliation:1. National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China;2. School of Kinesiology and Health, Capital University of Physical Education and Sports, Beijing 100191, China;3. University of Chinese Academy of Sciences, Beijing 100049, China
Abstract:Lipid droplets (LDs) are ubiquitous cellular organelles for lipid storage which are composed of a neutral lipid core bounded by a protein decorated phospholipid monolayer. Although lipid storage is their most obvious function, LDs are far from inert as they participate in maintaining lipid homeostasis through lipid synthesis, metabolism, and transportation. Furthermore, they are involved in cell signaling and other molecular events closely associated with human disease such as dyslipidemia, obesity, lipodystrophy, diabetes, fatty liver, atherosclerosis, and others. The last decade has seen a great increase in the attention paid to LD biology. Regardless, many fundamental features of LD biology remain obscure. In this review, we will discuss key aspects of LD biology including their biogenesis, growth and regression. We will also summarize the current knowledge about the role LDs play in human disease, especially from the perspective of the dynamics of the associated proteins. This article is part of a Special issue entitled Cardiac adaptations to obesity, diabetes and insulin resistance, edited by Professors Jan F.C. Glatz, Jason R.B. Dyck and Christine Des Rosiers.
Keywords:LDs  lipid droplets  PLIN1  perilipin  ADRP/PLIN2  adipocyte differentiation related protein  TAG  triacylglycerol  SE  sterol ester  GWS  genome-wide screens  ER  endoplasmic reticulum  FSP27  fat specific protein 27  Rab8a  ras-related protein Rab-8a  GDP  guanosine diphosphate  LPCAT1, 2  lysophosphatidylcholine acyltransferases 1 and 2  PC  phosphatidylcholine  ACSL3  long-chain acyl-coenzyme A synthetase 3  ATGL  adipose triglyceride lipase  HSL  hormone sensitive lipase  CD36  cluster of differentiation 36  FATP  fatty acid transport protein  AGPAT  1-acylglycerol-3-phosphate O-acyltransferase  LIPIN  phosphatidate phosphatase  RBPR  retinol binding protein receptor  CPT  carnitine palmitoyltransferase  ABCA1  ATP binding cassette aubfamily A member 1  ABCG1  ATP binding cassette subfamily G Member 1  SR-BI  scavenger receptor class B member 1  AS160  GTP  guanosine triphosphate  CCT1  CTP:phosphocholine cytidylyltransferase  PLIN3  TIP47  PLIN4  S3-12  PLIN5  OXPAT/MLDP/PAT-1  HCV  Hepatitis C Virus  ApoE  Apolipoprotein E  CGI-58  abhydrolase domain containing 5  MLDS  microorganism lipid droplet small  PKA  protein kinase A  CE  cholesteryl ester  acyl-CoA  acyl-coenzyme A  DGAT  acyl-CoA:diacylglycerol acyltransferase  ACAT  acyl-CoA:cholesterol acyltransferase  LART  lecithin:retinol acyltransferase  RE  retinyl ester  GPAT4  glycerol-3-phosphate acyltransferase 4  DAG  diacylglycerol  MAG  monoacylglycerol  MGL  monoacylglycerol lipase  FFA  free fatty acid  FASN  fatty acid synthase  DENV  dengue virus  AUP1  ancient ubiquitous protein 1  CIDE  cell death-inducing DFFA-like effector  IMCL  intramyocellular lipids  FC  free cholesterol  HDL  high density lipoproteins  nCEH  neutral cholesteryl ester hydrolase  CES1  carboxylesterase 1  NCEH1  neutral cholesterol ester hydrolase 1  LDAH  lipid droplet associated hydrolase  LDL  low density lipoprotein  NAFLD  nonalcoholic fatty liver disease  NASH  non-alcoholic steatohapatitis  HCC  hepatocellular carcinoma  PNPLA3  patatin like phospholipase domain containing 3  LIPC/HTGL  hepatic lipase  LYPLAL1  lysophospholipase-like1  17β-HSD13  17β-hydroxysteroid dehydrogenase 13  SCDR9  short-chain dehydrogenase/reductase 9  HSCs  hepatic stellate cells  WAT  white adipose tissue  ADHs  alcohol dehydrogenases  RAs  retinoic acids  RALDHs  retinaldehyde dehydrogenases  NLSD  neutral lipid storage disease  NLSDM  NLSD with severe myopathy  NLSDI  NLSD with ichthyosis  CGL  congenital generalized lipodystrophy  FPL  familial partial lipodystrophy  LPL  lipoprotein lipase  T2D  type 2 diabetes  ROS  reactive oxygen species  CHD  coronary heart disease  AD  Alzheimer's disease  MI  myocardial infarction  PAH  pulmonary arterial hypertension  CMT  Charcot-Marie-Tooth disease  Lipid droplets  Ectopic lipid storage  Metabolic diseases
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