Engineering a polarity-sensitive biosensor for time-lapse imaging of apoptotic processes and degeneration (original) (raw)
References
Kerr, J.F., Wyllie, A.H. & Currie, A.R. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br. J. Cancer26, 239–257 (1972). ArticleCASPubMedPubMed Central Google Scholar
Fadok, V.A. et al. Exposure of phosphatidylserine on the surface of apoptotic lymphocytes triggers specific recognition and removal by macrophages. J. Immunol.148, 2207–2216 (1992). CASPubMed Google Scholar
Koopman, G. et al. Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis. Blood84, 1415–1420 (1994). CASPubMed Google Scholar
Gavrieli, Y., Sherman, Y. & Ben-Sasson, S.A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J. Cell Biol.119, 493–501 (1992). ArticleCASPubMed Google Scholar
Martin, S.J. et al. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl. J. Exp. Med.182, 1545–1556 (1995). ArticleCASPubMed Google Scholar
Bretscher, M.S. Asymmetrical lipid bilayer structure for biological membranes. Nat. New Biol.236, 11–12 (1972). ArticleCASPubMed Google Scholar
Chan, A., Reiter, R., Wiese, S., Fertig, G. & Gold, R. Plasma membrane phospholipid asymmetry precedes DNA fragmentation in different apoptotic cell models. Histochem. Cell Biol.110, 553–558 (1998). ArticleCASPubMed Google Scholar
Rimon, G., Bazenet, C.E., Philpott, K.L. & Rubin, L.L. Increased surface phosphatidylserine is an early marker of neuronal apoptosis. J. Neurosci. Res.48, 563–570 (1997). ArticleCASPubMed Google Scholar
Seaton, B.A. (ed.) Annexins: Molecular Structure to Cellular Function. (R.G. Landes Company, Austin, Texas, USA, 1996). Google Scholar
Isas, J.M. et al. Calcium- and membrane-induced changes in the structure and dynamics of three helical hairpins in Annexin B12. Biochemistry44, 16435–16444 (2005). ArticleCASPubMed Google Scholar
Isas, J.M., Langen, R., Hubbell, W.L. & Haigler, H.T. Structure and dynamics of a helical hairpin that mediates calcium-dependent membrane binding of Annexin B12. J. Biol. Chem.279, 32492–32498 (2004). ArticleCASPubMed Google Scholar
Langen, R., Isas, J.M., Luecke, H., Haigler, H.T. & Hubbell, W.L. Membrane-mediated assembly of annexins studied by site-directed spin labeling. J. Biol. Chem.273, 22453–22457 (1998). ArticleCASPubMed Google Scholar
Vermes, I., Haanen, C., Steffens-Nakken, H. & Reutelingsperger, C. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. J. Immunol. Methods184, 39–51 (1995). ArticleCASPubMed Google Scholar
Karpinich, N.O., Tafani, M., Rothman, R.J., Russo, M.A. & Farber, J.L. The course of etoposide-induced apoptosis from damage to DNA and p53 activation to mitochondrial release of cytochrome c. J. Biol. Chem.277, 16547–16552 (2002). ArticleCASPubMed Google Scholar
Raff, M.C., Whitmore, A.V. & Finn, J.T. Axonal self-destruction and neurodegeneration. Science296, 868–871 (2002). ArticleCASPubMed Google Scholar
Goldstein, J.C., Waterhouse, N.J., Juin, P., Evan, G.I. & Green, D.R. The coordinate release of cytochrome c during apoptosis is rapid, complete and kinetically invariant. Nat. Cell Biol.2, 156–162 (2000). ArticleCASPubMed Google Scholar
Mirnikjoo, B., Balasubramanian, K. & Schroit, A.J. Mobilization of lysosomal calcium regulates the externalization of phosphatidylserine during apoptosis. J. Biol. Chem.284, 6918–6923 (2009). ArticleCASPubMedPubMed Central Google Scholar
Saxena, S. & Caroni, P. Mechanisms of axon degeneration: from development to disease. Prog. Neurobiol.83, 174–191 (2007). ArticleCASPubMed Google Scholar
Geske, F.J., Lieberman, R., Strange, R. & Gerschenson, L.E. Early stages of p53-induced apoptosis are reversible. Cell Death Differ.8, 182–191 (2001). ArticleCASPubMed Google Scholar
Hammill, A.K., Uhr, J.W. & Scheuermann, R.H. Annexin V staining due to loss of membrane asymmetry can be reversible and precede commitment to apoptotic death. Exp. Cell Res.251, 16–21 (1999). ArticleCASPubMed Google Scholar
Tang, H.L., Yuen, K.L., Tang, H.M. & Fung, M.C. Reversibility of apoptosis in cancer cells. Br. J. Cancer100, 118–122 (2009). ArticleCASPubMed Google Scholar
Nikolaev, A., McLaughlin, T., O'Leary, D.D. & Tessier-Lavigne, M. APP binds DR6 to trigger axon pruning and neuron death via distinct caspases. Nature457, 981–989 (2009). ArticleCASPubMedPubMed Central Google Scholar
Luecke, H., Chang, B.T., Mailliard, W.S., Schlaepfer, D.D. & Haigler, H.T. Crystal structure of the annexin XII hexamer and implications for bilayer insertion. Nature378, 512–515 (1995). ArticleCASPubMed Google Scholar
Mailliard, W.S., Luecke, H. & Haigler, H.T. Annexin XII forms calcium-dependent multimers in solution and on phospholipid bilayers: a chemical cross-linking study. Biochemistry36, 9045–9050 (1997). ArticleCASPubMed Google Scholar
Fischer, T., Lu, L., Haigler, H.T. & Langen, R. Annexin B12 is a sensor of membrane curvature and undergoes major curvature-dependent structural changes. J. Biol. Chem.282, 9996–10004 (2007). ArticleCASPubMed Google Scholar
Rosenberg, S.S., Kelland, E.E., Tokar, E., De la Torre, A.R. & Chan, J.R. The geometric and spatial constraints of the microenvironment induce oligodendrocyte differentiation. Proc. Natl. Acad. Sci. USA105, 14662–14667 (2008). ArticleCASPubMedPubMed Central Google Scholar