| Online-Ressource |
Verfasst von: | Pardo, Julián [VerfasserIn]  |
| Bosque, Alberto [VerfasserIn]  |
| Brehm, Reina [VerfasserIn]  |
| Wallich, Reinhard [VerfasserIn]  |
| Naval, Javier [VerfasserIn]  |
| Müllbacher, Arno [VerfasserIn]  |
| Anel, Alberto [VerfasserIn]  |
| Simon, Markus M. [VerfasserIn]  |
Titel: | Apoptotic pathways are selectively activated by granzyme A and/or granzyme B in CTL-mediated target cell lysis |
Verf.angabe: | Julián Pardo, Alberto Bosque, Reina Brehm, Reinhard Wallich, Javier Naval, Arno Müllbacher, Alberto Anel, and Markus M. Simon |
Jahr: | 2004 |
Umfang: | 12 S. |
Fussnoten: | Gesehen am 24.02.2021 |
Titel Quelle: | Enthalten in: The journal of cell biology |
Ort Quelle: | New York, NY : Rockefeller Univ. Press, 1962 |
Jahr Quelle: | 2004 |
Band/Heft Quelle: | 167(2004), 3, Seite 457-468 |
ISSN Quelle: | 1540-8140 |
Abstract: | Purified cytolytic T lymphocyte (CTL) proteases granzyme (gzm)A and gzmB with sublytic dose of perforin (perf) initiate distinct proapoptotic pathways. Their physiological relevance in CTL-mediated target cell apoptosis is elusive. Using ex vivo virus-immune CD8(+) T cells from mice deficient in perf, gzmA and/or gzmB, and the Fas-resistant EL4.F15 tumor target cell, we show that (a) CTL from gzmA(-/-) or gzmB(-/-) mice similarly induced early proapoptotic features, such as phosphatidyl serine (PS) exposure on plasma membrane, Delta Psi(m) loss, and reactive oxygen radical generation, though with distinct kinetics; (b) CTL from gzmA(-/-) but not from gzmB(-/-) mice activate caspase 3 and 9; (c) PS exposure induced by CTL from gzmA(-/-) or gzmB(-/-) mice is prevented, respectively, by caspase inhibitors or by reactive oxygen scavengers without interfering with target cell death; and (d) all gzm-induced apoptotic features analyzed depend critically on perf. Thus, perf is the principal regulator in CTL-mediated and gzm-facilitated intracellular processes. The ability of gzmA and gzmB to induce multiple independent cell death pathways may be the hosts response to circumvent evasion strategies of pathogens and tumors. |
DOI: | doi:10.1083/jcb.200406115 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
Volltext ; Verlag: https://doi.org/10.1083/jcb.200406115 |
| Volltext: https://rupress.org/jcb/article/167/3/457/51394 |
| DOI: https://doi.org/10.1083/jcb.200406115 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Sach-SW: | Animals |
| Apoptosis |
| Cell Line, Tumor |
| Cells, Cultured |
| Cytotoxicity, Immunologic |
| Granzymes |
| Kinetics |
| Membrane Glycoproteins |
| Membrane Potentials |
| Mice |
| Mice, Knockout |
| Perforin |
| Phosphatidylserines |
| Pore Forming Cytotoxic Proteins |
| Reactive Oxygen Species |
| Serine Endopeptidases |
| T-Lymphocytes, Cytotoxic |
| Time Factors |
K10plus-PPN: | 1749312670 |
Verknüpfungen: | → Zeitschrift |
Apoptotic pathways are selectively activated by granzyme A and/or granzyme B in CTL-mediated target cell lysis / Pardo, Julián [VerfasserIn]; 2004 (Online-Ressource)