CD5 + B cells are preferentially expanded in rabbit appendix: The role of CD5 in B cell development and selection
Although only a small proportion of mouse and human B cells are CD5 +, most adult rabbit B cells express CD5. However, CD5 was not detectable on the majority of B cells in neonatal appendix 1 and 3 days after birth. Cell trafficking studies demonstrated that CD5 + and CD5 − CD62L + B cells from bone...
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Veröffentlicht in: | Developmental and comparative immunology 2006, Vol.30 (8), p.711-722 |
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creator | Pospisil, Richard Alexander, Cornelius B. Obiakor, Harold Sinha, Rajesh K. Mage, Rose G. |
description | Although only a small proportion of mouse and human B cells are CD5
+, most adult rabbit B cells express CD5. However, CD5 was not detectable on the majority of B cells in neonatal appendix 1 and 3
days after birth. Cell trafficking studies demonstrated that CD5
+ and CD5
− CD62L
+ B cells from bone marrow migrated into appendix. There, CD5
+ B cells were preferentially expanded and predominated by ∼2
weeks of age. In mutant
ali/
ali rabbits, VHa2
+ B cells develop through gene conversion-like alteration of rearranged VH genes upstream of deleted VH1a2. Correlated appearance of individual CD5
+ germinal centers and VHa2
+ B-cells in mutant appendix suggests that CD5 binding positively selects cells with a2
+ framework regions that bind CD5. Following negative and positive selection, cells with diversified rearranged heavy- and light-chain sequences exit appendix, migrate to peripheral tissues and constitute the preimmune repertoire of CD5
+ B cells that encounter foreign antigens. |
doi_str_mv | 10.1016/j.dci.2005.10.001 |
format | Article |
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+, most adult rabbit B cells express CD5. However, CD5 was not detectable on the majority of B cells in neonatal appendix 1 and 3
days after birth. Cell trafficking studies demonstrated that CD5
+ and CD5
− CD62L
+ B cells from bone marrow migrated into appendix. There, CD5
+ B cells were preferentially expanded and predominated by ∼2
weeks of age. In mutant
ali/
ali rabbits, VHa2
+ B cells develop through gene conversion-like alteration of rearranged VH genes upstream of deleted VH1a2. Correlated appearance of individual CD5
+ germinal centers and VHa2
+ B-cells in mutant appendix suggests that CD5 binding positively selects cells with a2
+ framework regions that bind CD5. Following negative and positive selection, cells with diversified rearranged heavy- and light-chain sequences exit appendix, migrate to peripheral tissues and constitute the preimmune repertoire of CD5
+ B cells that encounter foreign antigens.</description><identifier>ISSN: 0145-305X</identifier><identifier>EISSN: 1879-0089</identifier><identifier>DOI: 10.1016/j.dci.2005.10.001</identifier><identifier>PMID: 16375969</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Amino Acid Sequence ; Animals ; appendix ; Appendix - cytology ; Appendix - immunology ; B-cells ; B-Lymphocytes - cytology ; B-Lymphocytes - immunology ; Base Sequence ; Bone Marrow - immunology ; CD5 ; CD5 Antigens - physiology ; gene conversion ; Gene Rearrangement, B-Lymphocyte, Heavy Chain ; Genes, Immunoglobulin ; Immunoglobulin Heavy Chains - genetics ; Immunoglobulin M ; Immunoglobulin Variable Region - genetics ; L-Selectin ; Molecular Sequence Data ; rabbit ; Rabbits - growth & development ; Rabbits - immunology ; Spleen - cytology ; Spleen - immunology ; superantigens ; trafficking ; VH-mutant ali/ ali</subject><ispartof>Developmental and comparative immunology, 2006, Vol.30 (8), p.711-722</ispartof><rights>2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-d95514289cab2ba6359ea90bf329168f76ad6531405e1edff72d77a20dff45a63</citedby><cites>FETCH-LOGICAL-c351t-d95514289cab2ba6359ea90bf329168f76ad6531405e1edff72d77a20dff45a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.dci.2005.10.001$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,4022,27922,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16375969$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pospisil, Richard</creatorcontrib><creatorcontrib>Alexander, Cornelius B.</creatorcontrib><creatorcontrib>Obiakor, Harold</creatorcontrib><creatorcontrib>Sinha, Rajesh K.</creatorcontrib><creatorcontrib>Mage, Rose G.</creatorcontrib><title>CD5 + B cells are preferentially expanded in rabbit appendix: The role of CD5 in B cell development and selection</title><title>Developmental and comparative immunology</title><addtitle>Dev Comp Immunol</addtitle><description>Although only a small proportion of mouse and human B cells are CD5
+, most adult rabbit B cells express CD5. However, CD5 was not detectable on the majority of B cells in neonatal appendix 1 and 3
days after birth. Cell trafficking studies demonstrated that CD5
+ and CD5
− CD62L
+ B cells from bone marrow migrated into appendix. There, CD5
+ B cells were preferentially expanded and predominated by ∼2
weeks of age. In mutant
ali/
ali rabbits, VHa2
+ B cells develop through gene conversion-like alteration of rearranged VH genes upstream of deleted VH1a2. Correlated appearance of individual CD5
+ germinal centers and VHa2
+ B-cells in mutant appendix suggests that CD5 binding positively selects cells with a2
+ framework regions that bind CD5. Following negative and positive selection, cells with diversified rearranged heavy- and light-chain sequences exit appendix, migrate to peripheral tissues and constitute the preimmune repertoire of CD5
+ B cells that encounter foreign antigens.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>appendix</subject><subject>Appendix - cytology</subject><subject>Appendix - immunology</subject><subject>B-cells</subject><subject>B-Lymphocytes - cytology</subject><subject>B-Lymphocytes - immunology</subject><subject>Base Sequence</subject><subject>Bone Marrow - immunology</subject><subject>CD5</subject><subject>CD5 Antigens - physiology</subject><subject>gene conversion</subject><subject>Gene Rearrangement, B-Lymphocyte, Heavy Chain</subject><subject>Genes, Immunoglobulin</subject><subject>Immunoglobulin Heavy Chains - genetics</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulin Variable Region - genetics</subject><subject>L-Selectin</subject><subject>Molecular Sequence Data</subject><subject>rabbit</subject><subject>Rabbits - growth & development</subject><subject>Rabbits - immunology</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>superantigens</subject><subject>trafficking</subject><subject>VH-mutant ali/ ali</subject><issn>0145-305X</issn><issn>1879-0089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtOwzAUhi0EoqXwACzIEwtKOE7iJIYJylWqxFIkNsuJT4Sr3LDTqn17HLUSG1580f9_8vkIuWQQMmDp7SrUpQkjAO7vIQA7IlOWZyIAyMUxmQJLeBAD_5qQM-dW4FfO4JRMWBpnXKRiSn7mT5ze0EdaYl07qizS3mKFFtvBqLreUdz2qtWoqWmpVUVhBqr6Hltttnd0-Y3UdjXSrqIjyWf2KKpxg3XXN55DfZ86rLEcTNeek5NK1Q4vDvuMfL48L-dvweLj9X3-sAjKmLMh0IJzlkS5KFURFSqNuUAloKjiSLA0r7JU6ZTHLAGODHVVZZHOMhWBPybc52fkes_tbfezRjfIxrjxa6rFbu1kmuURRAJ8kO2Dpe2c88PL3ppG2Z1kIEfPciW9Zzl6Hp-8Z9-5OsDXRYP6r3EQ6wP3-wD6ETcGrXSlwbZEbaz3IHVn_sH_ArcBjK0</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Pospisil, Richard</creator><creator>Alexander, Cornelius B.</creator><creator>Obiakor, Harold</creator><creator>Sinha, Rajesh K.</creator><creator>Mage, Rose G.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2006</creationdate><title>CD5 + B cells are preferentially expanded in rabbit appendix: The role of CD5 in B cell development and selection</title><author>Pospisil, Richard ; Alexander, Cornelius B. ; Obiakor, Harold ; Sinha, Rajesh K. ; Mage, Rose G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-d95514289cab2ba6359ea90bf329168f76ad6531405e1edff72d77a20dff45a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>appendix</topic><topic>Appendix - cytology</topic><topic>Appendix - immunology</topic><topic>B-cells</topic><topic>B-Lymphocytes - cytology</topic><topic>B-Lymphocytes - immunology</topic><topic>Base Sequence</topic><topic>Bone Marrow - immunology</topic><topic>CD5</topic><topic>CD5 Antigens - physiology</topic><topic>gene conversion</topic><topic>Gene Rearrangement, B-Lymphocyte, Heavy Chain</topic><topic>Genes, Immunoglobulin</topic><topic>Immunoglobulin Heavy Chains - genetics</topic><topic>Immunoglobulin M</topic><topic>Immunoglobulin Variable Region - genetics</topic><topic>L-Selectin</topic><topic>Molecular Sequence Data</topic><topic>rabbit</topic><topic>Rabbits - growth & development</topic><topic>Rabbits - immunology</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>superantigens</topic><topic>trafficking</topic><topic>VH-mutant ali/ ali</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pospisil, Richard</creatorcontrib><creatorcontrib>Alexander, Cornelius B.</creatorcontrib><creatorcontrib>Obiakor, Harold</creatorcontrib><creatorcontrib>Sinha, Rajesh K.</creatorcontrib><creatorcontrib>Mage, Rose G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Developmental and comparative immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pospisil, Richard</au><au>Alexander, Cornelius B.</au><au>Obiakor, Harold</au><au>Sinha, Rajesh K.</au><au>Mage, Rose G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD5 + B cells are preferentially expanded in rabbit appendix: The role of CD5 in B cell development and selection</atitle><jtitle>Developmental and comparative immunology</jtitle><addtitle>Dev Comp Immunol</addtitle><date>2006</date><risdate>2006</risdate><volume>30</volume><issue>8</issue><spage>711</spage><epage>722</epage><pages>711-722</pages><issn>0145-305X</issn><eissn>1879-0089</eissn><abstract>Although only a small proportion of mouse and human B cells are CD5
+, most adult rabbit B cells express CD5. However, CD5 was not detectable on the majority of B cells in neonatal appendix 1 and 3
days after birth. Cell trafficking studies demonstrated that CD5
+ and CD5
− CD62L
+ B cells from bone marrow migrated into appendix. There, CD5
+ B cells were preferentially expanded and predominated by ∼2
weeks of age. In mutant
ali/
ali rabbits, VHa2
+ B cells develop through gene conversion-like alteration of rearranged VH genes upstream of deleted VH1a2. Correlated appearance of individual CD5
+ germinal centers and VHa2
+ B-cells in mutant appendix suggests that CD5 binding positively selects cells with a2
+ framework regions that bind CD5. Following negative and positive selection, cells with diversified rearranged heavy- and light-chain sequences exit appendix, migrate to peripheral tissues and constitute the preimmune repertoire of CD5
+ B cells that encounter foreign antigens.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>16375969</pmid><doi>10.1016/j.dci.2005.10.001</doi><tpages>12</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Amino Acid Sequence Animals appendix Appendix - cytology Appendix - immunology B-cells B-Lymphocytes - cytology B-Lymphocytes - immunology Base Sequence Bone Marrow - immunology CD5 CD5 Antigens - physiology gene conversion Gene Rearrangement, B-Lymphocyte, Heavy Chain Genes, Immunoglobulin Immunoglobulin Heavy Chains - genetics Immunoglobulin M Immunoglobulin Variable Region - genetics L-Selectin Molecular Sequence Data rabbit Rabbits - growth & development Rabbits - immunology Spleen - cytology Spleen - immunology superantigens trafficking VH-mutant ali/ ali |
title | CD5 + B cells are preferentially expanded in rabbit appendix: The role of CD5 in B cell development and selection |
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