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A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates

There are two main classes of natural killer (NK) cell receptors in mammals, the killer cell immunoglobulin-like receptors (KIR) and the structurally unrelated killer cell lectin-like receptors (KLR). While KIR represent the most diverse group of NK receptors in all primates studied to date, includi...

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Autores principales: Averdam, Anne, Petersen, Beatrix, Rosner, Cornelia, Neff, Jennifer, Roos, Christian, Eberle, Manfred, Aujard, Fabienne, Münch, Claudia, Schempp, Werner, Carrington, Mary, Shiina, Takashi, Inoko, Hidetoshi, Knaust, Florian, Coggill, Penny, Sehra, Harminder, Beck, Stephan, Abi-Rached, Laurent, Reinhardt, Richard, Walter, Lutz
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757895/
https://www.ncbi.nlm.nih.gov/pubmed/19834558
http://dx.doi.org/10.1371/journal.pgen.1000688
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author Averdam, Anne
Petersen, Beatrix
Rosner, Cornelia
Neff, Jennifer
Roos, Christian
Eberle, Manfred
Aujard, Fabienne
Münch, Claudia
Schempp, Werner
Carrington, Mary
Shiina, Takashi
Inoko, Hidetoshi
Knaust, Florian
Coggill, Penny
Sehra, Harminder
Beck, Stephan
Abi-Rached, Laurent
Reinhardt, Richard
Walter, Lutz
author_facet Averdam, Anne
Petersen, Beatrix
Rosner, Cornelia
Neff, Jennifer
Roos, Christian
Eberle, Manfred
Aujard, Fabienne
Münch, Claudia
Schempp, Werner
Carrington, Mary
Shiina, Takashi
Inoko, Hidetoshi
Knaust, Florian
Coggill, Penny
Sehra, Harminder
Beck, Stephan
Abi-Rached, Laurent
Reinhardt, Richard
Walter, Lutz
author_sort Averdam, Anne
collection PubMed
description There are two main classes of natural killer (NK) cell receptors in mammals, the killer cell immunoglobulin-like receptors (KIR) and the structurally unrelated killer cell lectin-like receptors (KLR). While KIR represent the most diverse group of NK receptors in all primates studied to date, including humans, apes, and Old and New World monkeys, KLR represent the functional equivalent in rodents. Here, we report a first digression from this rule in lemurs, where the KLR (CD94/NKG2) rather than KIR constitute the most diverse group of NK cell receptors. We demonstrate that natural selection contributed to such diversification in lemurs and particularly targeted KLR residues interacting with the peptide presented by MHC class I ligands. We further show that lemurs lack a strict ortholog or functional equivalent of MHC-E, the ligands of non-polymorphic KLR in “higher” primates. Our data support the existence of a hitherto unknown system of polymorphic and diverse NK cell receptors in primates and of combinatorial diversity as a novel mechanism to increase NK cell receptor repertoire.
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spelling pubmed-27578952009-10-16 A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates Averdam, Anne Petersen, Beatrix Rosner, Cornelia Neff, Jennifer Roos, Christian Eberle, Manfred Aujard, Fabienne Münch, Claudia Schempp, Werner Carrington, Mary Shiina, Takashi Inoko, Hidetoshi Knaust, Florian Coggill, Penny Sehra, Harminder Beck, Stephan Abi-Rached, Laurent Reinhardt, Richard Walter, Lutz PLoS Genet Research Article There are two main classes of natural killer (NK) cell receptors in mammals, the killer cell immunoglobulin-like receptors (KIR) and the structurally unrelated killer cell lectin-like receptors (KLR). While KIR represent the most diverse group of NK receptors in all primates studied to date, including humans, apes, and Old and New World monkeys, KLR represent the functional equivalent in rodents. Here, we report a first digression from this rule in lemurs, where the KLR (CD94/NKG2) rather than KIR constitute the most diverse group of NK cell receptors. We demonstrate that natural selection contributed to such diversification in lemurs and particularly targeted KLR residues interacting with the peptide presented by MHC class I ligands. We further show that lemurs lack a strict ortholog or functional equivalent of MHC-E, the ligands of non-polymorphic KLR in “higher” primates. Our data support the existence of a hitherto unknown system of polymorphic and diverse NK cell receptors in primates and of combinatorial diversity as a novel mechanism to increase NK cell receptor repertoire. Public Library of Science 2009-10-16 /pmc/articles/PMC2757895/ /pubmed/19834558 http://dx.doi.org/10.1371/journal.pgen.1000688 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Averdam, Anne
Petersen, Beatrix
Rosner, Cornelia
Neff, Jennifer
Roos, Christian
Eberle, Manfred
Aujard, Fabienne
Münch, Claudia
Schempp, Werner
Carrington, Mary
Shiina, Takashi
Inoko, Hidetoshi
Knaust, Florian
Coggill, Penny
Sehra, Harminder
Beck, Stephan
Abi-Rached, Laurent
Reinhardt, Richard
Walter, Lutz
A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title_full A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title_fullStr A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title_full_unstemmed A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title_short A Novel System of Polymorphic and Diverse NK Cell Receptors in Primates
title_sort novel system of polymorphic and diverse nk cell receptors in primates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757895/
https://www.ncbi.nlm.nih.gov/pubmed/19834558
http://dx.doi.org/10.1371/journal.pgen.1000688
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