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Autophagy and Immunity Qingqing Wang Institute of Immunology Zhejiang University School of Medicine Nov 2, 2012 Autophagy Phagy = eating/lysosomal degradation Autophagy = self-eating Mechanism of breakdown of cytoplasm within the lysosome Autophagy: a basic cellular process in eukaryotes Autophagy  Highly conserved and regulated process that maintains cellular homeostasis and protects cells against starvation and microbe invasion Autophagy    Autophagosome: A double membrane bound compartment that engulfs cytosol and degrades the cytoplasmic contents. Large: 400-1500 nm May originate from ER or from fusion of lipid-containing vesicles that form ‘sequestration crescent’. Autophagic pathways  Plants and animals  Bacteria, viruses, parasites  Highly regulated processes  Stages: induction, execution, maturation Autophagy genes  Based on S. cerevisiae yeast studies.  ATG in yeast, homologs in other species.  Involved in:    Tumor suppression Starvation responses Preventing premature cell senescence 3 Stages    Initiation: nutrient starvation, growth factor-mediated starvation Execution Maturation Induction  TOR (Target Of Rapamycin) kinase  Inhibits autophagy when phosphorylated.  Also regulates protein and amino acid synthesis.   Rapamycin and nutrient starvation dephosphorylate TOR, inducing autophagy. Tamoxifen induces autophagy too (TOR?) Induction  Trimeric G proteins   High amino acids inactivate G proteins, so aa depletion may induce autophagy via G proteins. PI3Ks (Phosphatidylinositol-3-kinases)   Essential for starvation induced autophagy. 3-MA, wortmannin, LY294002 target PI3Ks, and result in inhibition of autophagy. Execution  Covalent linkage of Atg5 and Atg12  Covalent lipidation of Atg8  Enzymes Atg3, Atg7, and Atg10 are homologs of ubiquitylation enzymes but are used to modify pathway components instead of labeling them for degradation. Maturation  GTPases (Rab24) mediate vesicle fusion.  Intermediate autophagosomes    Fuse with endosomal vesicles. Acquire LAMP, accumulate DAMP proteins. Mature autolysosomes   Fuse with lysosomes. Acquire cathepsins and acid phosphatases. Detection methods  Microscopy   Biochemistry    Electron microscopy – ultrastructure, morphology, volumetrics, staining. Enzyme activity assays. Radioactive degradation studies. Marker studies   Autophagosomal or organelle markers. Fluorescence or immunodetection. The physilogical significance of autophagy  自噬参与代谢应激的保护机制  细胞自噬是细胞的看家者  自噬是染色体的守护者  细胞自噬决定细胞的生死 There are many ways to die… Programmed cell death Type I: caspase mediated Type II: autophagy-mediated Apoptosis  Programmed cell death      Type I: caspase mediated Type II: autophagy-mediated Entire cell dismantled within membrane-enclosed vesicles Taken up by phagocytes, preventing release of intracellular components from dying cells Normal morphogenesis, removing genetically damaged cells, proper tissue homeostasis, invading microbes Mechanism  Sequential activation of cysteine proteases (caspases)  Caspase 1-related: 1,4,5,13,14     Cytokine processing and pro-inflammatory cell death Initiator caspases: 2, 8, 9, 10 Effector caspases: 3,6,7 Regulated process   Extrinsic: stimulation of Fas or TNFR surface receptors Intrinsic: altered mitochondrial membrane integrity Necrosis      Cell swelling and rupture Release in intracellular components Activation of inflammatory response Can be regulated Can occur in concert with or instead of apoptosis (e.g. if apoptosis is blocked) Pyroptosis    Caspase-1-dependent cell death Convert IL-1B and IL-18 to active forms Induced by Shigella IpaB and Salmonella SipB Autophagy and diseases  Oncology  Liver  Breast  Colon  Lung Beclin-1 Myodegerative disease  Cardiac stress  a-antitrypsin deficiency ……    Brain     Alzheimer Multiple Sclerosis Parkinson’s disease Hungtingdon’s disease Miscellaneous  Cellular Process Apoptosis  Aging  Growth ……  Autophagy and immunity Antigen presentation  TLR signaling  Infection ……  Role of autophagy    Does autophagy benefit the host as a defense mechanism? Does autophagy benefit the microbe by facilitating survival and replication? Or both? Bacterial susceptibility    Astragalus-Mesorhizobium: Bacteria differentiate within membrane compartments until they can fix nitrogen and establish symbiosis. Nutrient starvation: bacterial degradation observed. Autophagy? http://www.bioscience.drexel.edu/Homepage/immunology/presentations/group6/Aintro.htm Bacterial susceptibility  Rickettsiae conorii    Sensitive to NO produced by IFN, TNF-α. Correlations between autophagosome-like structures and bacterial degradation. Are autophagosomes destroying bacteria or just cleaning up after bacteria are killed? Bacterial susceptibility  Listeria monocytogenes     Enter host cells by phagocytosis, escape from phagosomes, multiply in cytoplasm. ActA (actin) mutants are engulfed in autophagosome-like compartments. Wortmannin reduces bacterial entry into autophagosomes. Nutrient depletion increases bacterial entry into autophagosomes. http://www.rapidmicrobiology.com/news/603h48.php Bacterial subversion  Porphyromonas gingivalis  Infects human coronary artery endothelial cells.  Localizes to autophagosome-like compartments.  Wortmannin: compartments resembled lysosomes and acquired cathepsin earlier. Bacterial survival decreased. http://www.pgingivalis.org/ATCC33277(1).htm Bacterial subversion  Brucella abortus    Endosomal uptake, then autophagosomes. Wortmannin reduced survival, cell starvation increased survival. VirB mutants have Type IV secretion mutation that inhibits intracellular transport and growth. Mutants are localized to membrane compartments that acquire cathepsin earlier, resembling lysosomes. Bacterial subversion  Legionella pneumophila    Replicates in autophagosome-like compartments in macrophages. Dot/icm mutants are defective in Type IV secretion involved with organelle trafficking or intracellular multiplication. Mutants localized to lysosomal-like vesicles, not autophagosomes. ‘Pregnant pause’ model says that autophagosome maturation is delayed to allow for pathogen development. Bacterial subversion  Coxiella burnetti    Replicates within autophagosome-like acidic vesicles. Rab7 mutants had altered size and numbers of vesicles containing bacteria. Dot/icm homologs in Coxiella were able to return Dot/icm deficient Legionella to a wild phenotype. Viral susceptibility  Herpes-virus    PKR kinase – phosphorylates eukaryotic translation-initiation factor eIF2α to inhibit and deregulate cellular translation. PKR can also induce autophagy, apoptosis, and activate NF-KB. ICP34.5 – produced by herpes simplex virus 1 to antagonize PKR function by dephosphorylating eIF2α. Viral subversion  Positive-strand RNA viruses    Poliovirus, murine hepatitis virus (MHV), equine arterivirus (EAV), SARS human corona virus. Require membranes for replication. Autophagosomes are induced during infection, but are they part of the viral replication process or the host response to eliminate pathogens? TIP OF THE ICEBERG?
 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
									 
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                             
                                            