<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu H</submitter><funding>NIAID NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>e13780</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2967469</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(11)</volume><pubmed_abstract>MS4a4B, a CD20 homologue in T cells, is a novel member of the MS4A gene family in mice. The MS4A family includes CD20, FcεRIβ, HTm4 and at least 26 novel members that are characterized by their structural features: with four membrane-spanning domains, two extracellular domains and two cytoplasmic regions. CD20, FcεRIβ and HTm4 have been found to function in B cells, mast cells and hematopoietic cells respectively. However, little is known about the function of MS4a4B in T cell regulation. We demonstrate here that MS4a4B negatively regulates mouse T cell proliferation. MS4a4B is highly expressed in primary T cells, natural killer cells (NK) and some T cell lines. But its expression in all malignant T cells, including thymoma and T hybridoma tested, was silenced. Interestingly, its expressio</pubmed_abstract><journal>PloS one</journal><pubmed_title>MS4a4B, a CD20 homologue in T cells, inhibits T cell propagation by modulation of cell cycle.</pubmed_title><pmcid>PMC2967469</pmcid><funding_grant_id>R01 NS040085</funding_grant_id><funding_grant_id>NS040085</funding_grant_id><funding_grant_id>R01 AI070823</funding_grant_id><pubmed_authors>Zhang GX</pubmed_authors><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Rostami A</pubmed_authors><pubmed_authors>Williams MS</pubmed_authors><pubmed_authors>Carey GB</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Yan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>MS4a4B, a CD20 homologue in T cells, inhibits T cell propagation by modulation of cell cycle.</name><description>MS4a4B, a CD20 homologue in T cells, is a novel member of the MS4A gene family in mice. The MS4A family includes CD20, FcεRIβ, HTm4 and at least 26 novel members that are characterized by their structural features: with four membrane-spanning domains, two extracellular domains and two cytoplasmic regions. CD20, FcεRIβ and HTm4 have been found to function in B cells, mast cells and hematopoietic cells respectively. However, little is known about the function of MS4a4B in T cell regulation. We demonstrate here that MS4a4B negatively regulates mouse T cell proliferation. MS4a4B is highly expressed in primary T cells, natural killer cells (NK) and some T cell lines. But its expression in all malignant T cells, including thymoma and T hybridoma tested, was silenced. Interestingly, its expressio</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Nov</publication><modification>2025-04-05T13:40:13.512Z</modification><creation>2019-03-26T23:10:24Z</creation></dates><accession>S-EPMC2967469</accession><cross_references><pubmed>21072172</pubmed><doi>10.1371/journal.pone.0013780</doi></cross_references></HashMap>