共 208 条
Death by a thousand cuts: Granzyme pathways of programmed cell death
被引:478
作者:

Chowdhury, Dipanjan
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Radiat Oncol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Lieberman, Judy
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Immune Dis Inst, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Radiat Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Immune Dis Inst, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
关键词:
cytotoxic T lymphocyte;
cytotoxic granule;
natural killer cell;
serine protease;
granule exocytosis;
serpin;
D O I:
10.1146/annurev.immunol.26.021607.090404
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
The granzymes ire cell death-inducing enzymes, stored in the cytotoxic granules of cytotoxic T lymphocytes and natural killer cells, that are released during granule exocytosis when a specific virus-infected or transformed target cell is marked for elimination. Recent work suggests that this homologous family of serine esterases can activate at least three distinct pathways of cell death. This redundancy likely evolved to provide protection against pathogens and tumors with diverse strategies for evading cell death. This review discusses what is known about granzyme-mediated pathways of cell death as well as recent studies that implicate granzymes in immune regulation and extracellular proteolytic functions in inflammation.
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页码:389 / 420
页数:32
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共 208 条
- [1] Molecular ordering of the caspase activation cascade initiated by the cytotoxic T lymphocyte/natural killer (CTL/NK) protease granzyme B[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (06) : 4663 - 4673Adrain, C论文数: 0 引用数: 0 h-index: 0机构: Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, IrelandMurphy, BM论文数: 0 引用数: 0 h-index: 0机构: Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, IrelandMartin, SJ论文数: 0 引用数: 0 h-index: 0机构: Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland Trinity Coll Dublin, Smurfit Inst, Dept Genet, Mol Cell Biol Lab, Dublin 2, Ireland
- [2] A novel domain in adenovirus L4-100K is required for stable binding and efficient inhibition of human granzyme B: Possible interaction with a species-specific exosite[J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (17) : 6315 - 6326Andrade, F论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USACasciola-Rosen, LA论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USARosen, A论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
- [3] Adenovirus L4-100K assembly protein is a granzyme B substrate that potently inhibits granzyme B-mediated cell death[J]. IMMUNITY, 2001, 14 (06) : 751 - 761Andrade, F论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USABull, HG论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USAThornberry, NA论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USAKetner, GW论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USACasciola-Rosen, LA论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USARosen, A论文数: 0 引用数: 0 h-index: 0机构: Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
- [4] Granzyme H destroys the function of critical adenoviral proteins required for viral DNA replication and granzyme B inhibition[J]. EMBO JOURNAL, 2007, 26 (08) : 2148 - 2157Andrade, Felipe论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Mexico City, DF, MexicoFellows, Edward论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Mexico City, DF, MexicoJenne, Dieter E.论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Mexico City, DF, MexicoRosen, Antony论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Mexico City, DF, MexicoYoung, C. S. H.论文数: 0 引用数: 0 h-index: 0机构: Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Dept Immunol & Rheumatol, Mexico City, DF, Mexico
- [5] In vivo regulation of murine granzyme B gene transcription in activated primary T cells[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) : 16485 - 16493Babichuk, CK论文数: 0 引用数: 0 h-index: 0机构: Department of Biochemistry, University of Alberta, EdmontonDuggan, BL论文数: 0 引用数: 0 h-index: 0机构: Department of Biochemistry, University of Alberta, EdmontonBleackley, RC论文数: 0 引用数: 0 h-index: 0机构: Department of Biochemistry, University of Alberta, Edmonton
- [6] Mutational analysis of the murine granzyme B gene promoter in primary T cells and a T cell clone[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) : 18564 - 18571Babichuk, CK论文数: 0 引用数: 0 h-index: 0机构: UNIV ALBERTA,DEPT BIOCHEM,EDMONTON,AB T6G 2H7,CANADA UNIV ALBERTA,DEPT BIOCHEM,EDMONTON,AB T6G 2H7,CANADABleackley, RC论文数: 0 引用数: 0 h-index: 0机构: UNIV ALBERTA,DEPT BIOCHEM,EDMONTON,AB T6G 2H7,CANADA UNIV ALBERTA,DEPT BIOCHEM,EDMONTON,AB T6G 2H7,CANADA
- [7] Detection of soluble human granzyme K in vitro and in vivo[J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 2005, 35 (10) : 2940 - 2948Bade, B论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyLohrmann, J论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, Germanyten Brinke, A论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyWolbink, AM论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyWolbink, GJ论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, Germanyten Berge, IJM论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyVirchow, JC论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyLuttmann, W论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, GermanyHack, CE论文数: 0 引用数: 0 h-index: 0机构: Univ Med Clin Rostock, Dept Pneumol, D-18057 Rostock, Germany
- [8] Surface cathepsin B protects cytotoxic lymphocytes from self-destruction after degranulation[J]. JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (04) : 493 - 503Balaji, KN论文数: 0 引用数: 0 h-index: 0机构: NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USASchaschke, N论文数: 0 引用数: 0 h-index: 0机构: NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USAMachleidt, W论文数: 0 引用数: 0 h-index: 0机构: NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USACatalfamo, M论文数: 0 引用数: 0 h-index: 0机构: NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USAHenkart, PA论文数: 0 引用数: 0 h-index: 0机构: NCI, Expt Immunol Branch, NIH, Bethesda, MD 20892 USA
- [9] Cytotoxic T lymphocytes from cathepsin B-deficient mice survive normally in vitro and in vivo after encountering and killing target cells[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (41) : 30485 - 30491Baran, Katherine论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaCiccone, Annette论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaPeters, Christoph论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaYagita, Hideo论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaBird, Phillip I.论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaVilladangos, Jose A.论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, AustraliaTrapani, Joseph A.论文数: 0 引用数: 0 h-index: 0机构: Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, Australia
- [10] Antiviral cytokines induce hepatic expression of the granzyme B inhibitors, proteinase inhibitor 9 and serine proteinase inhibitor 6[J]. JOURNAL OF IMMUNOLOGY, 2004, 172 (10) : 6453 - 6459Barrie, MB论文数: 0 引用数: 0 h-index: 0机构: Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USAStout, HW论文数: 0 引用数: 0 h-index: 0机构: Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USAAbougergi, MS论文数: 0 引用数: 0 h-index: 0机构: Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USAMiller, BC论文数: 0 引用数: 0 h-index: 0机构: Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USAThiele, DL论文数: 0 引用数: 0 h-index: 0机构: Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA Univ Texas, SW Med Ctr, Dept Internal Med, Div Digest & Liver Dis, Dallas, TX 75390 USA