<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>108(2)</volume><submitter>Winkelmann R</submitter><pubmed_abstract>Krüppel-like factor 2 (KLF2) controls T lymphocyte egress from lymphoid organs by regulating sphingosin-1 phosphate receptor 1 (S1Pr1). Here we show that this is not the case for B cells. Instead, KLF2 controls homeostasis of B cells in peripheral lymphatic organs and homing of plasma cells to the bone marrow, presumably by controlling the expression of β(7)-integrin. In mice with a B cell-specific deletion of KLF2, S1Pr1 expression on B cells was only slightly affected. Accordingly, all splenic B cell subsets including B1 cells were present, but their numbers were increased with a clear bias for marginal zone (MZ) B cells. In contrast, fewer peyers patches harboring fewer B cells were found, and fewer B1 cells in the peritoneal cavity as well as recirculating B cells in the bone marrow we</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>710-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3021026</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>B cell homeostasis and plasma cell homing controlled by Kruppel-like factor 2.</pubmed_title><pmcid>PMC3021026</pmcid><pubmed_authors>Jack HM</pubmed_authors><pubmed_authors>Sandrock L</pubmed_authors><pubmed_authors>Porstner M</pubmed_authors><pubmed_authors>Reth M</pubmed_authors><pubmed_authors>Kahn ML</pubmed_authors><pubmed_authors>Schuh W</pubmed_authors><pubmed_authors>Roth E</pubmed_authors><pubmed_authors>Winkelmann R</pubmed_authors><pubmed_authors>Hobeika E</pubmed_authors><pubmed_authors>Mathews M</pubmed_authors></additional><is_claimable>false</is_claimable><name>B cell homeostasis and plasma cell homing controlled by Kruppel-like factor 2.</name><description>Krüppel-like factor 2 (KLF2) controls T lymphocyte egress from lymphoid organs by regulating sphingosin-1 phosphate receptor 1 (S1Pr1). Here we show that this is not the case for B cells. Instead, KLF2 controls homeostasis of B cells in peripheral lymphatic organs and homing of plasma cells to the bone marrow, presumably by controlling the expression of β(7)-integrin. In mice with a B cell-specific deletion of KLF2, S1Pr1 expression on B cells was only slightly affected. Accordingly, all splenic B cell subsets including B1 cells were present, but their numbers were increased with a clear bias for marginal zone (MZ) B cells. In contrast, fewer peyers patches harboring fewer B cells were found, and fewer B1 cells in the peritoneal cavity as well as recirculating B cells in the bone marrow we</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Jan</publication><modification>2025-05-18T13:23:23.077Z</modification><creation>2025-05-18T13:23:23.077Z</creation></dates><accession>S-EPMC3021026</accession><cross_references><pubmed>21187409</pubmed><doi>10.1073/pnas.1012858108</doi></cross_references></HashMap>