<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bezman NA</submitter><funding>NIAID NIH HHS</funding><funding>CIHR</funding><pagination>1000-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3572860</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(10)</volume><pubmed_abstract>Using whole-genome microarray data sets of the Immunological Genome Project, we demonstrate a closer transcriptional relationship between NK cells and T cells than between any other leukocytes, distinguished by their shared expression of genes encoding molecules with similar signaling functions. Whereas resting NK cells are known to share expression of a few genes with cytotoxic CD8(+) T cells, our transcriptome-wide analysis demonstrates that the commonalities extend to hundreds of genes, many encoding molecules with unknown functions. Resting NK cells demonstrate a 'preprimed' state compared with naive T cells, which allows NK cells to respond more rapidly to viral infection. Collectively, our data provide a global context for known and previously unknown molecular aspects of NK cell ide</pubmed_abstract><journal>Nature immunology</journal><pubmed_title>Molecular definition of the identity and activation of natural killer cells.</pubmed_title><pmcid>PMC3572860</pmcid><funding_grant_id>R24 AI072073</funding_grant_id><funding_grant_id>T32 AI060536</funding_grant_id><funding_grant_id>R01 AI067545</funding_grant_id><funding_grant_id>R01 AI100874</funding_grant_id><funding_grant_id>T32AI060536</funding_grant_id><funding_grant_id>R00 AI085035</funding_grant_id><funding_grant_id>AI072117</funding_grant_id><funding_grant_id>T32AI060537</funding_grant_id><funding_grant_id>T32 AI060537</funding_grant_id><funding_grant_id>R01 AI068129</funding_grant_id><pubmed_authors>Narayan K</pubmed_authors><pubmed_authors>Hardy RR</pubmed_authors><pubmed_authors>Randolph GJ</pubmed_authors><pubmed_authors>Monach P</pubmed_authors><pubmed_authors>Laidlaw D</pubmed_authors><pubmed_authors>Kim CC</pubmed_authors><pubmed_authors>Kamimura Y</pubmed_authors><pubmed_authors>Knell J</pubmed_authors><pubmed_authors>Jojic V</pubmed_authors><pubmed_authors>Davis S</pubmed_authors><pubmed_authors>Brown B</pubmed_authors><pubmed_authors>Gazit R</pubmed_authors><pubmed_authors>Benoist C</pubmed_authors><pubmed_authors>Kang J</pubmed_authors><pubmed_authors>Sylvia K</pubmed_authors><pubmed_authors>Min-Oo G</pubmed_authors><pubmed_authors>Wagers A</pubmed_authors><pubmed_authors>Brennan P</pubmed_authors><pubmed_authors>Mathis D</pubmed_authors><pubmed_authors>Malhotra D</pubmed_authors><pubmed_authors>Goldrath AW</pubmed_authors><pubmed_authors>Rossi DJ</pubmed_authors><pubmed_authors>Koller D</pubmed_authors><pubmed_authors>Kreslavsky T</pubmed_authors><pubmed_authors>Painter M</pubmed_authors><pubmed_authors>Shinton SA</pubmed_authors><pubmed_authors>Immunological Genome Project Consortium</pubmed_authors><pubmed_authors>Brenner M</pubmed_authors><pubmed_authors>Fletcher A</pubmed_authors><pubmed_authors>Jakubzick C</pubmed_authors><pubmed_authors>Lanier LL</pubmed_authors><pubmed_authors>Miller J</pubmed_authors><pubmed_authors>Merad M</pubmed_authors><pubmed_authors>Turley S</pubmed_authors><pubmed_authors>Kim F</pubmed_authors><pubmed_authors>Goldrath A</pubmed_authors><pubmed_authors>Collins JJ</pubmed_authors><pubmed_authors>Bezman NA</pubmed_authors><pubmed_authors>Gautier Em</pubmed_authors><pubmed_authors>Heng T</pubmed_authors><pubmed_authors>Jianu R</pubmed_authors><pubmed_authors>Hendricks DW</pubmed_authors><pubmed_authors>Cohen N</pubmed_authors><pubmed_authors>Sun JC</pubmed_authors><pubmed_authors>Shay T</pubmed_authors><pubmed_authors>Elpek K</pubmed_authors><pubmed_authors>Ericson J</pubmed_authors><pubmed_authors>Best JA</pubmed_authors><pubmed_authors>Rao TN</pubmed_authors><pubmed_authors>Regev A</pubmed_authors><pubmed_authors>Bellemare-Pelletier A</pubmed_authors><pubmed_authors>Best AJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular definition of the identity and activation of natural killer cells.</name><description>Using whole-genome microarray data sets of the Immunological Genome Project, we demonstrate a closer transcriptional relationship between NK cells and T cells than between any other leukocytes, distinguished by their shared expression of genes encoding molecules with similar signaling functions. Whereas resting NK cells are known to share expression of a few genes with cytotoxic CD8(+) T cells, our transcriptome-wide analysis demonstrates that the commonalities extend to hundreds of genes, many encoding molecules with unknown functions. Resting NK cells demonstrate a 'preprimed' state compared with naive T cells, which allows NK cells to respond more rapidly to viral infection. Collectively, our data provide a global context for known and previously unknown molecular aspects of NK cell ide</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Oct</publication><modification>2025-04-19T17:19:57.597Z</modification><creation>2019-03-27T01:04:51Z</creation></dates><accession>S-EPMC3572860</accession><cross_references><pubmed>22902830</pubmed><doi>10.1038/ni.2395</doi></cross_references></HashMap>