Colourful death: Six-parameter classification of cell death by flow cytometry—Dead cells tell tales

The response of the immune system against dying and dead cells strongly depends on the cell death phenotype. Beside other forms of cell death, two clearly distinct populations, early apoptotic and secondary necrotic cells, have been shown to induce anti-inflammation/tolerance and inflammation/immune priming, respectively. Cytofluorometry is a powerful technique to detect morphological and phenotypical changes occurring during cell death. Here, we describe a new technique using AnnexinA5, propidiumiodide, DiIC1(5) and Hoechst 33342 to sub-classify populations of apoptotic and/or necrotic cells. The method allows the fast and reliable identification of several different phases and pathways of cell death by analysing the following cell death associated changes in a single tube: cellular granularity and shrinkage, phosphatidylserine exposure, ion selectivity of the plasma membrane, mitochondrial membrane potential, and DNA content. The clear characterisation of cell death is of major importance for instance in immunization studies, in experimental therapeutic settings, and in the exploration of cell-death associated diseases. It also enables the analysis of immunological properties of distinct populations of dying cells and the pathways involved in this process.

[1]  M. Herrmann,et al.  Phospholipids: Key Players in Apoptosis and Immune Regulation , 2009, Molecules.

[2]  G. Kroemer,et al.  Reduction in mitochondrial potential constitutes an early irreversible step of programmed lymphocyte death in vivo , 1995, The Journal of experimental medicine.

[3]  Elisa Nemes,et al.  Multiparametric analysis of cells with different mitochondrial membrane potential during apoptosis by polychromatic flow cytometry , 2007, Nature Protocols.

[4]  G. Gores,et al.  Irreversible injury in anoxic hepatocytes precipitated by an abrupt increase in plasma membrane permeability , 1988, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  Dipankar Koley,et al.  Triton X-100 concentration effects on membrane permeability of a single HeLa cell by scanning electrochemical microscopy (SECM) , 2010, Proceedings of the National Academy of Sciences.

[6]  K. Lauber,et al.  CRP/anti-CRP Antibodies Assembly on the Surfaces of Cell Remnants Switches Their Phagocytic Clearance Toward Inflammation , 2011, Front. Immun..

[7]  S. Saini,et al.  Melittin activates endogenous phospholipase D during cytolysis of human monocytic leukemia cells. , 1999, Toxicon : official journal of the International Society on Toxinology.

[8]  M. Hengartner The biochemistry of apoptosis , 2000, Nature.

[9]  G. Schett,et al.  Monosodium urate crystals induce extracellular DNA traps in neutrophils, eosinophils, and basophils but not in mononuclear cells , 2012, Front. Immun..

[10]  A. Wyllie,et al.  Apoptosis: A Basic Biological Phenomenon with Wide-ranging Implications in Tissue Kinetics , 1972, British Journal of Cancer.

[11]  I Nicoletti,et al.  A rapid and simple method for measuring thymocyte apoptosis by propidium iodide staining and flow cytometry. , 1991, Journal of immunological methods.

[12]  C. Walsh,et al.  Programmed necrosis and autophagy in immune function , 2012, Immunological reviews.

[13]  M. Hoeve,et al.  Clearance of apo Nph induces an immunosuppressive response in pro-inflammatory type-1 and anti-inflammatory type-2 MΦ , 2009, Autoimmunity.

[14]  G. Schett,et al.  IgG opsonized nuclear remnants from dead cells cause systemic inflammation in SLE , 2010, Autoimmunity.

[15]  R. Zucker,et al.  Comparison of cellular and nuclear flow cytometric techniques for discriminating apoptotic subpopulations. , 1994, Experimental cell research.

[16]  J. Fletcher,et al.  Possible mechanisms of action of cobra snake venom cardiotoxins and bee venom melittin. , 1993, Toxicon : official journal of the International Society on Toxinology.

[17]  M. Lamkanfi,et al.  Inflammasomes: Caspase-1-Activating Platforms with Critical Roles in Host Defense , 2010, Front. Microbio..

[18]  M. Herrmann,et al.  Inflammatory clearance of apoptotic remnants in systemic lupus erythematosus (SLE). , 2008, Autoimmunity reviews.

[19]  R. Stoika,et al.  Apoptosis-related changes in plasma membrane glycoconjugates of peripheral blood lymphocytes in rheumatoid arthritis , 2009, Autoimmunity.

[20]  H. Jäck,et al.  After shrinkage apoptotic cells expose internal membrane-derived epitopes on their plasma membranes , 2008, Cell Death and Differentiation.

[21]  W. Buzgariu,et al.  Autophagy in Hydra: a response to starvation and stress in early animal evolution. , 2009, Biochimica et biophysica acta.

[22]  John Savill,et al.  A blast from the past: clearance of apoptotic cells regulates immune responses , 2002, Nature Reviews Immunology.

[23]  C. Hohenadl,et al.  UV-B Irradiated Cell Lines Execute Programmed Cell Death in Various Forms , 1998, Apoptosis.

[24]  G.,et al.  Annexin V for Flow Cytometric Detection of Phosphatidylserine Expression on B Cells Undergoing Apoptosis , 2000 .

[25]  U. Gaipl Waste: An important immune modulator , 2009, Autoimmunity.

[26]  P. Sheard,et al.  Changes in mitochondrial membrane potential during staurosporine‐induced apoptosis in Jurkat cells , 2000, FEBS letters.

[27]  J. Kerr,et al.  Patterns of cell death. , 1988, Methods and achievements in experimental pathology.

[28]  H. Sherratt Mitochondria: structure and function. , 1991, Revue neurologique.

[29]  M. Herrmann,et al.  When autologous chromatin becomes a foe , 2012, Autoimmunity.

[30]  W. Van den Broeck,et al.  Morphological and Biochemical Aspects of Apoptosis, Oncosis and Necrosis , 2002, Anatomia, histologia, embryologia.

[31]  G. Schett,et al.  Treatment with DNAse I fosters binding to nec PBMC of CRP , 2009, Autoimmunity.