STRUCTURAL CHANGES IN MITOCHONDRIAL MEMBRANES DURING APOPTOSIS

细胞凋亡过程中线粒体膜的结构变化

• 批准号: 8172267
• 负责人: KATHLEEN W. KINNALLY
• 金额: $ 0.54万
• 依托单位: WADSWORTH CENTER
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-07 至 2011-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8172267
• 关键词: Antibodies; Apoptosis; Apoptotic; Appearance; Atomic Force Microscopy; BAX gene; BH4 Domain; Bax protein; Caliber; Cell Death; Cell Line; Cells; Cessation of life; Computer Retrieval of Information on Scientific Projects Database; Consensus; Cultured Cells; Cytolysis; Cytosol; Defect; Double-Blind Method; Family member; Functional disorder; Funding; Gold Colloid; Grant; Image; Immunoglobulin G; Individual; Induction of Apoptosis; Institution; Interleukin-3; Label; Link; Lipids; Liposomes; Mammalian Cell; Membrane; Mitochondria; Mus; Negative Staining; Outer Mitochondrial Membrane; Pathway interactions; Penetration; Permeability; Play; Process; Proteins; Reporting; Research; Research Personnel; Resolution; Resources; Sampling; Screening procedure; Source; Specific qualifier value; Staging; Time; United States National Institutes of Health; Voltage-Dependent Anion Channel; Yeasts; abstracting; base; cytochrome c; deprivation; electron tomography; mitochondrial membrane; novel; pro-apoptotic protein; research study; respiratory

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. ABSTRACT: During the early stages of apoptosis, the pro-apoptotic protein Bax moves from the cytosol to the mitochondrial outer membrane (OM) where it oligomerizes and initiates a process that results in release of cytochrome c and other proteins from the intermembrane space (IMS) into the cytosol (Wei et al., 2000). This process is initiated by the truncated form of the protein Bid (tBid) and is inhibited by anti-apoptotic proteins like Bcl-2. There are several hypotheses in play regarding the mechanism of release of cytochrome c, including (1) the formation of large pores in the OM by Bax and possibly other proteins, such as the channel VDAC; (2) the formation of structural defects in the OM, perhaps involving lipids like ceremides; and (3) inner membrane expansion, causing OM lysis, perhaps at regions weakened by Bax (e.g., Korsmeyer et al., 2000; Shimizu et al., 2000; Mootha et al., 2001; Degterev et al., 2001; Waterhouse et al., 2002). Strong support for hypothesis (1) has been provided by electrophysiological studies indicating the appearance of a new channel activity in mitochondrial outer membranes concurrent with release of cytochrome c during early stages of apoptosis induced by IL-3 deprivation in murine FL5.12 cells (Pavlov et al., 2001). That the new channel (called MAC for Mitochondrial Apoptosis-induced Channel) might be the cytochrome c release pathway is suggested by two observations. First, its maximum conductance amplitudes are consistent with permeability to proteins having diameters of 5 nm or larger (the diameter of cytochrome c is around 3 nm). Second, cytochrome c and other basic proteins cause a transient blockade of the channel conductance, consistent with penetration and possible translocation (although the latter has not been directly demonstrated). First experiments will be done with mitochondria isolated from the murine cell line at the specified times following induction of apoptosis, prepared for negative-stain TEM. At this resolution, the largest MAC pores expected on the basis of conductance amplitude (approximately 8-10 nm) should be detectable especially if MAC forms clusters. Immuno-labelling of mitochondria with anti-Bax antibodies suggests that Bax does cluster on the OM. We will employ immuno-labeling of intact mitochondria with anti-Bax and anti-cytochrome c antibodies (commercially available). Decoration of OM regions by the distinctive IgG molecules (in the absence of colloidal gold-labeled secondary antibody) may help to localize the structural features we hope to characterize. It should be noted in this regard that pores 5-200 nm in diameter have been detected in flattened Bax-treated liposomes by atomic force microscopy (Epand et al. 2002). While there is no guarantee that we will detect the structural basis for cytochrome c release from mitochondria in these studies, we will  at the very least  establish a lower limit for the physical size of the pore or other membrane structural feature underlying this very important phenomenon. References. 1. Degterev, A., Boyce, M., and Yuan, J. (2001). The channel of death. J Cell Biol 155:695-697. 2. Epand, R. F., Martinou, J. C., Montessuit, S., Epand, R. M., and Yip, C. M. (2002). Direct evidence for membrane pore formation by the apoptotic protein Bax. Biochem Biophys Res Comm 298:744-749. 3. Korsmeyer, S. J., Wei, M. C., Saito, M., Weiler, S., Oh, K. J., and Schlesinger, P. H. (2000). Pro-apoptotic cascade activates BID, which oligomerizes BAK or BAX into pores that result in the release of cytochrome c. Cell Death Differ 7:1166-1173. 4. Kuwana, T., Mackey, M., Perkins, G., Ellisman, M., Latterich, M., Schneiter, R., Green, D. R., and Newmeyer, D. D. (2002). Bid, Bax, and lipids cooperate to form supramolecular openings in the outer mitochondrial membrane. Cell 111:331-342. 5. Mootha, V. K., Wei, M. C., Buttle, K., Scorrano, L., Panoutsakopoulou, V., Mannella, C. A., and Korsmeyer, S. J. (2001). A reversible component of mitochondrial respiratory dysfunction in apoptosis can be rescued by exogenous cytochrome c. EMBO J 20:661-671. 6. Pavlov, E. V., Priault, M., Pietkiewicz, D., Cheng, E. H. Y., Antonsson, B., Manon, S., Korsmeyer, S. J., Mannella, C. A., and Kinnally, K. W. (2001). A novel, high conductance channel of mitochondria linked to apoptosis in mammalian cells and Bax expression in yeast. J Cell Biol 155:719-724. 7. Penczek, P., Marko, M., Buttle, K., and Frank, J. (1995). Double-tilt electron tomography. Ultramicroscopy 60:393-410. 8. Shimizu, S., Konishi, A., Kodama, T., and Tsujimoto, Y. (2000). BH4 domain of antiapoptotic Bcl-2 family members closes voltage-dependent anion channel and inhibits apoptotic mitochondrial changes and cell death. Proc Natl Acad Sci USA 97:3100-3105. 9. Waterhouse, N. J., Ricci, J.-E., and Green, D. R. (2002). All of a sudden it's over: mitochondrial outer-membrane permeabilization in apoptosis. Biochimie 84:113-121. In the Previous reporting period, Christian Renken made several trips to NYU to prepare TEM samples of mitochondrial membranes from control and apoptotic culture cells for characterization of changes in the outer membrane associated with induction of the large channel (MAC) responsible for cytochrome c transport. The first approach was to image hundreds of isolated outer membranes flat-embedded first in negative stain to determine whether there are discrete novel structural features in membranes from apoptotic cells, using double-blind screening by multiple individuals. If found, such consensus features will be used as references in larger-scale correlation searches, to attempt to compute 2D averages of MAC.

这个子项目是众多研究子项目之一