In vivo primed mouse T cells selectively express T cell-specific serine proteinase-1 and the proteinase-like molecules granzyme B and C
Previous studies have shown that mouse CD8+ T lymphocyte clones (TLC) produce T cell-specific serine protelnase-1 (MTSP-1) as well as a family of six homologous molecules, termed granzymes B–G, which are structurally related to serine protelnases. Of these proteins, only MTSP-1 has been studied in d...
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Veröffentlicht in: | International immunology 1991-01, Vol.3 (1), p.9-19 |
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description | Previous studies have shown that mouse CD8+ T lymphocyte clones (TLC) produce T cell-specific serine protelnase-1 (MTSP-1) as well as a family of six homologous molecules, termed granzymes B–G, which are structurally related to serine protelnases. Of these proteins, only MTSP-1 has been studied in detail. It has been shown to occur in the majority of CD8+ and a fraction of CD4+ T effector cells in vivo and in vitro and has demonstrable enzyme activity in these cells. The presence of the other serine proteinase-like molecules in T cells is less well defined. We have now analyzed the expression of mRNA species specific for granzymes B–G In activated T cell populations using the sensitive polymerase chain reaction which allows the detection of mRNA species from as little as 2 pg of total cytoplasmlc RNA. We demonstrate that MTSP-1 and all six serine proteinase-like transcripts are expressed in a panel of four CD8+ and six CD4+ long-term-cultured TLC, though at greatly differing concentrations. In contrast, in vivo primed T cells of both phenotypes, CD4+ and CD8+, and in vitro activated T cells derived from short-term cultures only express mRNA species specific for MTSP-1 and CCP1 and little of those for CCP2, but no transcripts for granzymes D–G. These findings argue against the participation of granzymes D–G in T cell-mediated functions in vivo. |
doi_str_mv | 10.1093/intimm/3.1.9 |
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Of these proteins, only MTSP-1 has been studied in detail. It has been shown to occur in the majority of CD8+ and a fraction of CD4+ T effector cells in vivo and in vitro and has demonstrable enzyme activity in these cells. The presence of the other serine proteinase-like molecules in T cells is less well defined. We have now analyzed the expression of mRNA species specific for granzymes B–G In activated T cell populations using the sensitive polymerase chain reaction which allows the detection of mRNA species from as little as 2 pg of total cytoplasmlc RNA. We demonstrate that MTSP-1 and all six serine proteinase-like transcripts are expressed in a panel of four CD8+ and six CD4+ long-term-cultured TLC, though at greatly differing concentrations. In contrast, in vivo primed T cells of both phenotypes, CD4+ and CD8+, and in vitro activated T cells derived from short-term cultures only express mRNA species specific for MTSP-1 and CCP1 and little of those for CCP2, but no transcripts for granzymes D–G. 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Of these proteins, only MTSP-1 has been studied in detail. It has been shown to occur in the majority of CD8+ and a fraction of CD4+ T effector cells in vivo and in vitro and has demonstrable enzyme activity in these cells. The presence of the other serine proteinase-like molecules in T cells is less well defined. We have now analyzed the expression of mRNA species specific for granzymes B–G In activated T cell populations using the sensitive polymerase chain reaction which allows the detection of mRNA species from as little as 2 pg of total cytoplasmlc RNA. We demonstrate that MTSP-1 and all six serine proteinase-like transcripts are expressed in a panel of four CD8+ and six CD4+ long-term-cultured TLC, though at greatly differing concentrations. In contrast, in vivo primed T cells of both phenotypes, CD4+ and CD8+, and in vitro activated T cells derived from short-term cultures only express mRNA species specific for MTSP-1 and CCP1 and little of those for CCP2, but no transcripts for granzymes D–G. These findings argue against the participation of granzymes D–G in T cell-mediated functions in vivo.</description><subject>Animals</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Granzymes</subject><subject>Lymphocyte Activation</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>mRNA expression</subject><subject>Polymerase Chain Reaction</subject><subject>proteolytic enzymes</subject><subject>RNA - genetics</subject><subject>RNA, Complementary</subject><subject>Serine Endopeptidases - biosynthesis</subject><subject>Serine Endopeptidases - genetics</subject><subject>T lymphocytes</subject><subject>T-Lymphocytes - enzymology</subject><subject>T-Lymphocytes - immunology</subject><issn>0953-8178</issn><issn>1460-2377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9Lw0AQxRdRtP65eRX25MnUnWySzR41qBUEQSoUL8tmM9HVJK3ZtLR-Ab-2W1MUT54G5v3mMTOPkGNgQ2CSn9ums3V9zocwlFtkAFHCgpALsU0GTMY8SEGke2TfuVfGGA8l3yW7IPxoGA_I521DF3YxpbPW1ljQejp3SMfUYFU56rBC09kFViuKy1mLzm20wM3Q2NIaz7S2QT8_7dA22mEAVDcF7V7-NCv7ht7d-80rdPS51c3HqkZ6-Q1nh2Sn1JXDo009II_XV-NsFNzd39xmF3eBCQXrAsgjjMDkTPOSRwLQxHmRJEXKWJgCh0KUhU5kzg1HNCkgi41OBQomIixL4AfktPf1q73P0XWqtm59kG7Qn65SlgCPI_YvCLGENAbhwbMeNO3UuRZLtX6lblcKmFoHpPqAFFegpMdPNr7z3D_8F-4T8XrQ69Z1uPyRdfumEsFFrEaTJzWRD1kmQaoR_wJd2541</recordid><startdate>199101</startdate><enddate>199101</enddate><creator>Ebnet, Klaus</creator><creator>Tapia, Johanna Chluba-de</creator><creator>Hurtenbach, Ursula</creator><creator>Kramer, Michael D.</creator><creator>Simon, Markus M.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199101</creationdate><title>In vivo primed mouse T cells selectively express T cell-specific serine proteinase-1 and the proteinase-like molecules granzyme B and C</title><author>Ebnet, Klaus ; Tapia, Johanna Chluba-de ; Hurtenbach, Ursula ; Kramer, Michael D. ; Simon, Markus M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-1b4e41cb0a3f3471ec5bd66d80028131d7fda69b3c3eec81e05ca87e7074eff13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animals</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Granzymes</topic><topic>Lymphocyte Activation</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>mRNA expression</topic><topic>Polymerase Chain Reaction</topic><topic>proteolytic enzymes</topic><topic>RNA - genetics</topic><topic>RNA, Complementary</topic><topic>Serine Endopeptidases - biosynthesis</topic><topic>Serine Endopeptidases - genetics</topic><topic>T lymphocytes</topic><topic>T-Lymphocytes - enzymology</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ebnet, Klaus</creatorcontrib><creatorcontrib>Tapia, Johanna Chluba-de</creatorcontrib><creatorcontrib>Hurtenbach, Ursula</creatorcontrib><creatorcontrib>Kramer, Michael D.</creatorcontrib><creatorcontrib>Simon, Markus M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ebnet, Klaus</au><au>Tapia, Johanna Chluba-de</au><au>Hurtenbach, Ursula</au><au>Kramer, Michael D.</au><au>Simon, Markus M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo primed mouse T cells selectively express T cell-specific serine proteinase-1 and the proteinase-like molecules granzyme B and C</atitle><jtitle>International immunology</jtitle><addtitle>Int Immunol</addtitle><date>1991-01</date><risdate>1991</risdate><volume>3</volume><issue>1</issue><spage>9</spage><epage>19</epage><pages>9-19</pages><issn>0953-8178</issn><eissn>1460-2377</eissn><abstract>Previous studies have shown that mouse CD8+ T lymphocyte clones (TLC) produce T cell-specific serine protelnase-1 (MTSP-1) as well as a family of six homologous molecules, termed granzymes B–G, which are structurally related to serine protelnases. Of these proteins, only MTSP-1 has been studied in detail. It has been shown to occur in the majority of CD8+ and a fraction of CD4+ T effector cells in vivo and in vitro and has demonstrable enzyme activity in these cells. The presence of the other serine proteinase-like molecules in T cells is less well defined. We have now analyzed the expression of mRNA species specific for granzymes B–G In activated T cell populations using the sensitive polymerase chain reaction which allows the detection of mRNA species from as little as 2 pg of total cytoplasmlc RNA. We demonstrate that MTSP-1 and all six serine proteinase-like transcripts are expressed in a panel of four CD8+ and six CD4+ long-term-cultured TLC, though at greatly differing concentrations. In contrast, in vivo primed T cells of both phenotypes, CD4+ and CD8+, and in vitro activated T cells derived from short-term cultures only express mRNA species specific for MTSP-1 and CCP1 and little of those for CCP2, but no transcripts for granzymes D–G. These findings argue against the participation of granzymes D–G in T cell-mediated functions in vivo.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>1710925</pmid><doi>10.1093/intimm/3.1.9</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Female Gene Expression Granzymes Lymphocyte Activation Mice Mice, Inbred Strains mRNA expression Polymerase Chain Reaction proteolytic enzymes RNA - genetics RNA, Complementary Serine Endopeptidases - biosynthesis Serine Endopeptidases - genetics T lymphocytes T-Lymphocytes - enzymology T-Lymphocytes - immunology |
title | In vivo primed mouse T cells selectively express T cell-specific serine proteinase-1 and the proteinase-like molecules granzyme B and C |
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