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dc.creatorMolinero, Luciana Lorena-
dc.creatorFuertes, Mercedes Beatriz-
dc.creatorRabinovich, Gabriel Adrián-
dc.creatorLeonardo Fainboim-
dc.creatorZwirner, Norberto Walter-
dc.date2017-12-14T22:27:54Z-
dc.date2017-12-14T22:27:54Z-
dc.date2002-05-
dc.date2017-12-04T18:00:24Z-
dc.date.accessioned2019-04-29T15:46:27Z-
dc.date.available2019-04-29T15:46:27Z-
dc.date.issued2002-05-
dc.identifierMolinero, Luciana Lorena; Fuertes, Mercedes Beatriz; Rabinovich, Gabriel Adrián; Leonardo Fainboim; Zwirner, Norberto Walter; Activation-induced expression of MICA on T lymphocytes involves engagement of CD3 and CD28; Federation of American Societies for Experimental Biology; Journal of Leukocyte Biology; 71; 5; 5-2002; 791-797-
dc.identifier0741-5400-
dc.identifierhttp://hdl.handle.net/11336/30713-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/301641-
dc.descriptionMICA is an HLA-related cell stress-regulated antigen recognized by cytotoxic cells expressing the NKG2D molecule. Although resting lymphocytes do not express MICA, it can be induced on PHA-activated T cells. Here, we demonstrate by Western blot that MICA is induced on allogeneic-activated CD4(+) and CD8(+) T lymphocytes. Blocking activation with anti-HLA class I, anti-HLA-DR, or anti-CD86 mAb affected the expression of MICA slightly. When T cells were stimulated with anti-CD3 or anti-CD28 mAb plus PMA, a sustained up-regulation of MICA was observed by Western blot, RT-PCR, and flow cytometry. The expression of MICA reached a plateau at day 4 after CD3 engagement and at day 3 after anti-CD28/PMA stimulation. Conversely, the proliferative response reached a peak at day 4. Hence, CD3 or CD28 engagement induces MICA expression on T lymphocytes. This activation-induced expression might participate in NKG2D-mediated cytotoxicity toward activated T cells to maintain homeostasis during an ongoing immune response.-
dc.descriptionFil: Molinero, Luciana Lorena. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina-
dc.descriptionFil: Fuertes, Mercedes Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina-
dc.descriptionFil: Rabinovich, Gabriel Adrián. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina-
dc.descriptionFil: Leonardo Fainboim. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina-
dc.descriptionFil: Zwirner, Norberto Walter. Universidad de Buenos Aires. Facultad de Medicina. Hospital de Clínicas General San Martín; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Biología y Medicina Experimental. Fundación de Instituto de Biología y Medicina Experimental. Instituto de Biología y Medicina Experimental; Argentina-
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dc.languageeng-
dc.publisherFederation of American Societies for Experimental Biology-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.jleukbio.org/content/71/5/791.abstract-
dc.relationinfo:eu-repo/semantics/altIdentifier/pmid/11994503-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectMICA-
dc.subjectNKG2D-
dc.subjectT CELLS-
dc.subjectInmunología-
dc.subjectMedicina Básica-
dc.subjectCIENCIAS MÉDICAS Y DE LA SALUD-
dc.titleActivation-induced expression of MICA on T lymphocytes involves engagement of CD3 and CD28-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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