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pubmed-article:12182453pubmed:dateCreated2002-8-16lld:pubmed
pubmed-article:12182453pubmed:abstractTextLy49 antigens, interacting with MHC class I molecules, enable NK cells to distinguish "self" from "non-self". Here, we investigated the activating receptor Ly49 D after allogeneic bone marrow transplantation (BMT). After transplantation of B6 bone marrow (BM) into BALB/c recipients we observed a significant reduction of Ly49 D+ NK cells and a decreased density of expression. We found a nonstochastic distribution of Ly49 D with Ly49 G2. In contrast to reduced coexpression with Ly49 A, a constant rate of Ly49 G2 on Ly49 D+ NK cells was observed in allogeneic chimeras. Cytotoxicity was reduced during the first two months after BMT After this time allogeneic chimeras showed tolerance against host-specific targets. We conclude that NK cells are able to shape their Lys49 repertoire fitting to a new environment after allogeneic BMT. This alteration seems to depend on the presence of new corresponding MHC class I molecules resulting in downregulation of respective receptors on donor cells. Analysing coexpression of Ly49 D and Ly49 G2, we found a relationship between these two receptors, showing a distinct effect after allogeneic BMT. Functional data indicate that a time of reduced NK cell cytotoxicity after BMT is followed by in vitro tolerance of allogeneic chimeras.lld:pubmed
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pubmed-article:12182453pubmed:volume205lld:pubmed
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pubmed-article:12182453pubmed:pagination267-81lld:pubmed
pubmed-article:12182453pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:12182453pubmed:articleTitleModulation of Ly49 D expression after allogeneic bone marrow transplantation and functional consequences.lld:pubmed
pubmed-article:12182453pubmed:affiliationAbteilung Klinische Immunologie, Medizinische Hochschule Hannover, Germany.lld:pubmed
pubmed-article:12182453pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12182453pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed