Activation-driven T cell death. I. Requirements for de novo transcription and translation and association with genome fragmentation
We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag r...
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Veröffentlicht in: | The Journal of immunology (1950) 1989-12, Vol.143 (11), p.3461-3469 |
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description | We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag receptor complex and other activation structures on the T cell surface, such as Thy-1 and Ly-6. The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. We hypothesize that activation-driven cell death may be involved in vivo in the clonal deletion of auto-reactive T cells during T cell ontogeny. |
doi_str_mv | 10.4049/jimmunol.143.11.3461 |
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The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. 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I. Requirements for de novo transcription and translation and association with genome fragmentation</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag receptor complex and other activation structures on the T cell surface, such as Thy-1 and Ly-6. The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. We hypothesize that activation-driven cell death may be involved in vivo in the clonal deletion of auto-reactive T cells during T cell ontogeny.</description><subject>Animals</subject><subject>Antibody Specificity</subject><subject>Antigens, Ly - immunology</subject><subject>Antigens, Surface - immunology</subject><subject>Cell Survival</subject><subject>Cytotoxicity, Immunologic</subject><subject>DNA Damage</subject><subject>Epitopes - immunology</subject><subject>Hybridomas - immunology</subject><subject>Hybridomas - metabolism</subject><subject>Kinetics</subject><subject>Lectins - immunology</subject><subject>Lymphocyte Activation</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred CBA</subject><subject>Protein Biosynthesis</subject><subject>Receptors, Antigen, T-Cell - immunology</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>T-Lymphocytes, Cytotoxic - metabolism</subject><subject>Thy-1 Antigens</subject><subject>Transcription, Genetic</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1DAUhi0EKsPAG4DkFWKT4Lsny6qCUqkSEipry3WOZ1wl9tROJmLNi5M0Q8WOlXX8X6zjD6H3lNSCiObzQ-j7MaaupoLXlNZcKPoCbaiUpFKKqJdoQwhjFdVKv0ZvSnkghCjCxAW6YEI3Sjcb9PvSDeFkh5Bi1eZwgojvsIOuwy3Y4VDjmxr_gMcxZOghDgX7lGcJx3RKeMg2FpfDcYljG9v1prPPsy0lubDOUxgOeA8x9YB9tvul70l5i1552xV4dz636OfXL3dX36rb79c3V5e3leNM00oJqq2STJIdVa0HYC0QTbhud0Jppp0HrSXnzErhdvcAlGhP3Lywbbn0nm_Rx7X3mNPjCGUwfSjLrjZCGovRDedaN_S_RiqFVHR-a4vEanQ5lZLBm2MOvc2_DCVmgWT-QjIzJEOpWSDNsQ_n_vG-h_Y5dKYy659W_RD2h2n-elN623Wzm5ppmv6t-gOj1J9y</recordid><startdate>19891201</startdate><enddate>19891201</enddate><creator>Ucker, DS</creator><creator>Ashwell, JD</creator><creator>Nickas, G</creator><general>Am Assoc Immnol</general><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>19891201</creationdate><title>Activation-driven T cell death. 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Requirements for de novo transcription and translation and association with genome fragmentation</title><author>Ucker, DS ; Ashwell, JD ; Nickas, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3271-6417a65250816dfee2de07037d846727cfe775332a54c8bee107f0c024ad35ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Antibody Specificity</topic><topic>Antigens, Ly - immunology</topic><topic>Antigens, Surface - immunology</topic><topic>Cell Survival</topic><topic>Cytotoxicity, Immunologic</topic><topic>DNA Damage</topic><topic>Epitopes - immunology</topic><topic>Hybridomas - immunology</topic><topic>Hybridomas - metabolism</topic><topic>Kinetics</topic><topic>Lectins - immunology</topic><topic>Lymphocyte Activation</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred CBA</topic><topic>Protein Biosynthesis</topic><topic>Receptors, Antigen, T-Cell - immunology</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>T-Lymphocytes, Cytotoxic - metabolism</topic><topic>Thy-1 Antigens</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ucker, DS</creatorcontrib><creatorcontrib>Ashwell, JD</creatorcontrib><creatorcontrib>Nickas, G</creatorcontrib><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>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ucker, DS</au><au>Ashwell, JD</au><au>Nickas, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Activation-driven T cell death. I. Requirements for de novo transcription and translation and association with genome fragmentation</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>1989-12-01</date><risdate>1989</risdate><volume>143</volume><issue>11</issue><spage>3461</spage><epage>3469</epage><pages>3461-3469</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>We have observed that stimuli that are mitogenic for normal T cells can induce cell death in transformed T cell hybridomas. "Activation-driven cell death" can be triggered by the presentation of appropriate Ag as well as by treatment with lectins and antibodies specific for the T cell Ag receptor complex and other activation structures on the T cell surface, such as Thy-1 and Ly-6. The activation-driven lethal process is cell autonomous, is associated with a fragmentation of the cell's genome characteristic of the "suicide process" induced in immature T cells by glucocorticoids and in target cells by cytotoxic T lymphocytes, and is dependent upon transcription and translation, presumably associated with the expression of new gene products. We hypothesize that activation-driven cell death may be involved in vivo in the clonal deletion of auto-reactive T cells during T cell ontogeny.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>2479679</pmid><doi>10.4049/jimmunol.143.11.3461</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibody Specificity Antigens, Ly - immunology Antigens, Surface - immunology Cell Survival Cytotoxicity, Immunologic DNA Damage Epitopes - immunology Hybridomas - immunology Hybridomas - metabolism Kinetics Lectins - immunology Lymphocyte Activation Mice Mice, Inbred BALB C Mice, Inbred CBA Protein Biosynthesis Receptors, Antigen, T-Cell - immunology T-Lymphocytes, Cytotoxic - immunology T-Lymphocytes, Cytotoxic - metabolism Thy-1 Antigens Transcription, Genetic |
title | Activation-driven T cell death. I. Requirements for de novo transcription and translation and association with genome fragmentation |
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