<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu LG</submitter><funding>NIAID NIH HHS</funding><pagination>248-58</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3244560</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>188(1)</volume><pubmed_abstract>B cells play a critical role in the initialization and development of the systemic lupus erythematosus that is dependent on the expression of the endosomal ssRNA receptor TLR7. Previous studies have established that B cell expression of TLR7 is controlled by the type I IFN secreted by plasmacytoid dendritic cells. In this article, we report that VISA, also known as MAVS, IPS-1, and CardIf, essential for RIG-I/MDA5-mediated signaling following sensing of cytosolic RNA, regulate B cell expression of TLR7 and CD23. We found that B cells from a VISA(-/-) mouse express reduced TLR7 but normal basal levels of type I IFN. We also show that although IFN-β and TLR7 agonists synergize to promote TLR7 expression in VISA(-/-) B cells, they do not fully complement the defect seen in VISA(-/-) cells. Ce</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>VISA is required for B cell expression of TLR7.</pubmed_title><pmcid>PMC3244560</pmcid><funding_grant_id>P01 AI022295</funding_grant_id><funding_grant_id>P01AI022295022</funding_grant_id><funding_grant_id>P01 AI022295-22</funding_grant_id><funding_grant_id>R01 AI062739-05S1</funding_grant_id><funding_grant_id>R01 AI062739-05S2</funding_grant_id><funding_grant_id>R01 AI062739-05</funding_grant_id><funding_grant_id>R01 AI062739</funding_grant_id><funding_grant_id>R01AI062739-05</funding_grant_id><funding_grant_id>R01AI062739-05S2</funding_grant_id><funding_grant_id>R01AI062739-05S1</funding_grant_id><pubmed_authors>Zhang BC</pubmed_authors><pubmed_authors>Xu LG</pubmed_authors><pubmed_authors>Akerlund LJ</pubmed_authors><pubmed_authors>Shu HB</pubmed_authors><pubmed_authors>Jin L</pubmed_authors><pubmed_authors>Cambier JC</pubmed_authors></additional><is_claimable>false</is_claimable><name>VISA is required for B cell expression of TLR7.</name><description>B cells play a critical role in the initialization and development of the systemic lupus erythematosus that is dependent on the expression of the endosomal ssRNA receptor TLR7. Previous studies have established that B cell expression of TLR7 is controlled by the type I IFN secreted by plasmacytoid dendritic cells. In this article, we report that VISA, also known as MAVS, IPS-1, and CardIf, essential for RIG-I/MDA5-mediated signaling following sensing of cytosolic RNA, regulate B cell expression of TLR7 and CD23. We found that B cells from a VISA(-/-) mouse express reduced TLR7 but normal basal levels of type I IFN. We also show that although IFN-β and TLR7 agonists synergize to promote TLR7 expression in VISA(-/-) B cells, they do not fully complement the defect seen in VISA(-/-) cells. Ce</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Jan</publication><modification>2025-04-18T17:24:39.376Z</modification><creation>2019-03-26T23:42:55Z</creation></dates><accession>S-EPMC3244560</accession><cross_references><pubmed>22105994</pubmed><doi>10.4049/jimmunol.1100918</doi></cross_references></HashMap>