Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/3420
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dc.creatorRuíz Vela, Antonio-
dc.creatorSerrano Gómez, Fernando-
dc.creatorGonzález de la Peña, Manuel Angel-
dc.creatorAbad, José Luis-
dc.creatorBernad, Antonio-
dc.creatorMaki, Masatoshi-
dc.creatorMartínez-Alonso, Carlos-
dc.date2008-04-02T11:47:16Z-
dc.date2008-04-02T11:47:16Z-
dc.date2001-08-
dc.date.accessioned2017-01-31T01:01:26Z-
dc.date.available2017-01-31T01:01:26Z-
dc.identifierThe Journal of Experimental Medicine, volume 194, number 3, august 6, 2001, pp. 247–254-
dc.identifier0022-1007-
dc.identifierhttp://hdl.handle.net/10261/3420-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/3420-
dc.descriptionCopyright © by The Rockefeller University Press-
dc.descriptionLong-term cultured pre-B cells are able to differentiate into immunoglobulin (Ig)M-positive B cells (IgM cells) when transplanted into severe combined immunodeficient (SCID) mice. Based on previous studies, here we report the development of a reconstitution assay in nonobese diabetic/SCID (NOD/SCID) mice using pre-B cells, which allows us to study the role of calpains (calcium-activated endopeptidases) during B cell development as well as in B cell clonal deletion. Using this model, we show that calpastatin (the natural inhibitor of calpains) inhibits B cell receptor–induced apoptosis in IgM cells derived from transplanted mice. We thus hypothesize an important function for calpain in sculpting the B cell repertoire.-
dc.descriptionPeer reviewed-
dc.format455975 bytes-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherRockefeller University Press-
dc.rightsopenAccess-
dc.subjectpre-B cells-
dc.subjectCalpastatin-
dc.subjectCalpain-
dc.subjectBCR-
dc.subjectTransplant-
dc.titleTransplanted long-term cultured pre-BI cells expressing calpastatin are resistant to B cell receptor–induced apoptosis-
dc.typeArtículo-
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