Residual Cytotoxicity and Granzyme K Expression in Granzyme A-deficient Cytotoxic Lymphocytes*

Cytotoxic lymphocytes contain granules that have the ability to induce apoptosis in susceptible target cells. The granule contents include perforin, a pore-forming molecule, and several granzymes, including A and B, which are the most abundant serine proteases in these granules. Granzyme B-deficient cytotoxic T lymphocytes (CTL) have a severe defect in their ability to rapidly induce apoptosis in their targets, but have an intact late cytotoxicity pathway that is in part perforin-dependent. In this report, we have created mice that are deficient for granzyme A and characterized their phenotype. These mice have normal growth and development and normal lymphocyte development, activation, and proliferation. Granzyme A-deficient CTL have a small but reproducible defect in their ability to induce 51Cr and125I-UdR release from susceptible allogeneic target cells. Since other granzyme A-like tryptases could potentially account for the residual cytotoxicity in granzyme A-deficient CTL, we cloned the murine granzyme K gene, which is linked to granzyme A in humans, and proved that it is also tightly linked with murine granzyme A. The murine granzyme K gene (which encodes a tryptase similar to granzyme A) is expressed at much lower levels than granzyme A in CTL and LAK cells, but its expression is unaltered in granzyme A−/− mice. The minimal cytotoxic defect in granzyme A−/− CTL could be due to the existence of an intact, functional early killing pathway (granzyme B dependent), or to the persistent expression of additional granzyme tryptases like granzyme K.

[1]  T. Ley,et al.  Mechanisms responsible for granzyme B-independent cytotoxicity. , 1997, Blood.

[2]  T. Ley,et al.  Long-range disruption of gene expression by a selectable marker cassette. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[3]  K. Ebnet,et al.  Granzyme A is critical for recovery of mice from infection with the natural cytopathic viral pathogen, ectromelia. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[4]  T. Sayers,et al.  Cloning and expression of a second human natural killer cell granule tryptase, HNK‐Tryp‐2/granzyme 3 , 1996, Journal of leukocyte biology.

[5]  T. Ley,et al.  The role of granzyme B in murine models of acute graft-versus-host disease and graft rejection. , 1996, Blood.

[6]  K. Ebnet,et al.  Granzyme A‐deficient mice retain potent cell‐mediated cytotoxicity. , 1995, The EMBO journal.

[7]  T. Ley,et al.  Natural killer and lymphokine-activated killer cells require granzyme B for the rapid induction of apoptosis in susceptible target cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[8]  B. Schmidt,et al.  Cloning of cDNA for human granzyme 3 , 1995, FEBS letters.

[9]  P. Henkart,et al.  Synergistic roles of granzymes A and B in mediating target cell death by rat basophilic leukemia mast cell tumors also expressing cytolysin/perforin , 1995, Journal of Experimental Medicine.

[10]  Timothy J. Ley,et al.  Cytotoxic lymphocytes require granzyme B for the rapid induction of DNA fragmentation and apoptosis in allogeneic target cells , 1994, Cell.

[11]  T. Sayers,et al.  Purification and cloning of a novel serine protease, RNK-Tryp-2, from the granules of a rat NK cell leukemia. , 1994, Journal of Immunology.

[12]  J. Trapani,et al.  Met-ase: cloning and distinct chromosomal location of a serine protease preferentially expressed in human natural killer cells. , 1993, Journal of immunology.

[13]  P. Lichter,et al.  The human granzyme A (HFSP, CTLA3) gene maps to 5q11-q12 and defines a new locus of the serine protease superfamily. , 1993, Genomics.

[14]  I. Weissman,et al.  Genomic organization of the mouse granzyme A gene. Two mRNAs encode the same mature granzyme A with different leader peptides. , 1992, Journal of Biological Chemistry.

[15]  J. Trapani,et al.  Purification and cloning of a novel serine protease, RNK-Met-1, from the granules of a rat natural killer cell leukemia. , 1992, The Journal of biological chemistry.

[16]  R. Aebersold,et al.  Purification of three cytotoxic lymphocyte granule serine proteases that induce apoptosis through distinct substrate and target cell interactions , 1992, The Journal of experimental medicine.

[17]  J. Shiver,et al.  Cytotoxicity with target DNA breakdown by rat basophilic leukemia cells expressing both cytolysin and granzyme A , 1992, Cell.

[18]  K. Ebnet,et al.  Organization of the gene encoding the mouse T-cell-specific serine proteinase "granzyme A". , 1992, Genomics.

[19]  R. Aebersold,et al.  A natural killer cell granule protein that induces DNA fragmentation and apoptosis , 1992, The Journal of experimental medicine.

[20]  T. Sayers,et al.  Purification of a factor from the granules of a rat natural killer cell line (RNK) that reduces tumor cell growth and changes tumor morphology. Molecular identity with a granule serine protease (RNKP-1). , 1992, Journal of immunology.

[21]  J. Seidman,et al.  Embryonic stem cells lacking a functional inhibitory G-protein subunit (alpha i2) produced by gene targeting of both alleles. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[22]  R. D. Hanson,et al.  Structure and expression of a cluster of human hematopoietic serine protease genes found on chromosome 14q11.2. , 1991, The Journal of biological chemistry.

[23]  D. Hudig,et al.  RNKP-1, a novel natural killer-associated serine protease gene cloned from RNK-16 cytotoxic lymphocytes. , 1990, Journal of immunology.

[24]  R. D. Hanson,et al.  A cluster of hematopoietic serine protease genes is found on the same chromosomal band as the human alpha/delta T-cell receptor locus. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Haefliger,et al.  Isolation and complete structure of the lymphocyte serine protease granzyme G, a novel member of the granzyme multigene family in murine cytolytic T lymphocytes. Evolutionary origin of lymphocyte proteases. , 1989, Biochemistry.

[26]  P. Henkart,et al.  Induction of target cell DNA release by the cytotoxic T lymphocyte granule protease granzyme A , 1989, The Journal of experimental medicine.

[27]  T. Ley,et al.  Globin gene expression in erythroid human fetal liver cells. , 1989, The Journal of clinical investigation.

[28]  A. Lanzavecchia,et al.  Characterization of granzymes A and B isolated from granules of cloned human cytotoxic T lymphocytes. , 1988, Journal of immunology.

[29]  G. McFadden,et al.  Organization of two genes encoding cytotoxic T lymphocyte-specific serine proteases CCPI and CCPII. , 1988, Biochemistry.

[30]  J. Trapani,et al.  Molecular cloning of an inducible serine esterase gene from human cytotoxic lymphocytes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[31]  C. Lobe,et al.  Isolation of two cDNA sequences which encode cytotoxic cell proteases , 1988, FEBS letters.

[32]  J. Haefliger,et al.  Identification and sequencing of cDNA clones encoding the granule-associated serine proteases granzymes D, E, and F of cytolytic T lymphocytes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[33]  A. Caputo,et al.  Structure and differential mechanisms of regulation of expression of a serine esterase gene in activated human T lymphocytes. , 1988, The Journal of biological chemistry.

[34]  I. Weissman,et al.  Cloning and chromosomal assignment of a human cDNA encoding a T cell- and natural killer cell-specific trypsin-like serine protease. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[35]  C. Weissmann,et al.  Induction of mRNA for a serine protease and a beta-thromboglobulin-like protein in mitogen-stimulated human leukocytes. , 1987, Journal of immunology.

[36]  J. Tschopp,et al.  A family of serine esterases in lytic granules of cytolytic T lymphocytes , 1987, Cell.

[37]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[38]  M. Kramer,et al.  A novel serine proteinase (HuTSP) isolated from a cloned human CD8+ cytolytic T cell line is expressed and secreted by activated CD4+ and CD8+ lymphocytes , 1987, European journal of immunology.

[39]  H. Simon,et al.  Purification and characterization of a T cell specific serine proteinase (TSP‐1) from cloned cytolytic T lymphocytes. , 1986, The EMBO journal.

[40]  Chau‐Ching Liu,et al.  Isolation and characterization of a serine esterase from cytolytic T cell granules , 1986, Cell.

[41]  C. Verret,et al.  Serine esterase in cytolytic T lymphocytes , 1986, Nature.

[42]  F. Denizot,et al.  The inducible cytotoxic T-lymphocyte-associated gene transcript CTLA-1 sequence and gene localization to mouse chromosome 14 , 1986, Nature.

[43]  I. Weissman,et al.  Cloning of a cDNA for a T cell-specific serine protease from a cytotoxic T lymphocyte. , 1986, Science.

[44]  B. Finlay,et al.  Novel serine proteases encoded by two cytotoxic T lymphocyte-specific genes. , 1986, Science.

[45]  P. Henkart Mechanism of lymphocyte-mediated cytotoxicity. , 1985, Annual review of immunology.

[46]  J. Russell,et al.  Mechanisms of immune lysis. III. Characterization of the nature and kinetics of the cytotoxic T lymphocyte-induced nuclear lesion in the target. , 1982, Journal of immunology.

[47]  E. Shaw,et al.  Thiobenzyl benzyloxycarbonyl-L-lysinate, substrate for a sensitive colorimetric assay for trypsin-like enzymes. , 1979, Analytical biochemistry.