Regulated expression of peripheral node addressin-positive high endothelial venules controls seeding of B lymphocytes into developing neonatal rabbit appendix
Young rabbit appendix is a homologue of chicken bursa of Fabricius; both are crucial sites for preimmune B-cell repertoire diversification. Here, we report that appendix regulates precursor lymphocyte recruitment for further development by modulating the sites of extravasation. The total area of per...
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description | Young rabbit appendix is a homologue of chicken bursa of Fabricius; both are crucial sites for preimmune B-cell repertoire diversification. Here, we report that appendix regulates precursor lymphocyte recruitment for further development by modulating the sites of extravasation. The total area of peripheral node addressin-positive (PNAd
+) high endothelial venules (HEVs) increased from 1 day to 1 week after birth, remained constant up to 2 weeks and declined to a low and persistent amount by 3 weeks. In normal 1-week and manipulated 5-week appendix where growth of follicles was retarded, PNAd
+ HEVs were present in the basolateral sides of B-cell follicles whereas, in normal 5-wk-appendix these were restricted to T-cell areas. The PNAd was expressed on the lumenal surface of HEVs. The proportions of CD62L
+ B cells in appendix declined from ∼40% at 3 days to 2–3% at 4 weeks. In lymphocyte transfer experiments, CD62L
+ B cells were preferentially recruited compared with CD62L
− B cells, anti-PNAd antibody blocked migration of B cells by ∼50%, and 100 times more B cells were recruited in 1-week compared to 6-week appendix. Thus, a unique spatiotemporal expression pattern of PNAd
+ HEVs is associated with development of B-cell follicles. This regulates migration of blood-borne B-lymphocytes into developing appendix by interacting with CD62L. |
doi_str_mv | 10.1016/j.vetimm.2005.09.009 |
format | Article |
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+) high endothelial venules (HEVs) increased from 1 day to 1 week after birth, remained constant up to 2 weeks and declined to a low and persistent amount by 3 weeks. In normal 1-week and manipulated 5-week appendix where growth of follicles was retarded, PNAd
+ HEVs were present in the basolateral sides of B-cell follicles whereas, in normal 5-wk-appendix these were restricted to T-cell areas. The PNAd was expressed on the lumenal surface of HEVs. The proportions of CD62L
+ B cells in appendix declined from ∼40% at 3 days to 2–3% at 4 weeks. In lymphocyte transfer experiments, CD62L
+ B cells were preferentially recruited compared with CD62L
− B cells, anti-PNAd antibody blocked migration of B cells by ∼50%, and 100 times more B cells were recruited in 1-week compared to 6-week appendix. Thus, a unique spatiotemporal expression pattern of PNAd
+ HEVs is associated with development of B-cell follicles. This regulates migration of blood-borne B-lymphocytes into developing appendix by interacting with CD62L.</description><identifier>ISSN: 0165-2427</identifier><identifier>EISSN: 1873-2534</identifier><identifier>EISSN: 1365-2567</identifier><identifier>DOI: 10.1016/j.vetimm.2005.09.009</identifier><identifier>PMID: 16249036</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>animal age ; animal proteins ; Animals ; Animals, Newborn ; Antigens, Surface - immunology ; Appendix ; Appendix - immunology ; B lymphocyte recruitment ; B-lymphocyte migration ; B-lymphocytes ; B-Lymphocytes - immunology ; Cell Movement - immunology ; endothelium ; Flow Cytometry ; food animals ; gene expression ; genes ; immune system ; immunoglobulins ; Immunohistochemistry ; l-Selectin ; L-Selectin - immunology ; Lymphatic Vessels - immunology ; Membrane Proteins - immunology ; neonatal development ; neonates ; perifpheral node addressin-positive high endothelial venules ; PNAd ; rabbits ; Rabbits - immunology ; small intestine ; temporal variation</subject><ispartof>Veterinary Immunology and Immunopathology, 2006-03, Vol.110 (1), p.97-108</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-d06ccc25ff75264b6b7719e6c070caa92da161808f7502f0b5add955692e542f3</citedby><cites>FETCH-LOGICAL-c415t-d06ccc25ff75264b6b7719e6c070caa92da161808f7502f0b5add955692e542f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0165242705002916$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16249036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinha, Rajesh K.</creatorcontrib><creatorcontrib>Alexander, Cornelius</creatorcontrib><creatorcontrib>Mage, Rose G.</creatorcontrib><title>Regulated expression of peripheral node addressin-positive high endothelial venules controls seeding of B lymphocytes into developing neonatal rabbit appendix</title><title>Veterinary Immunology and Immunopathology</title><addtitle>Vet Immunol Immunopathol</addtitle><description>Young rabbit appendix is a homologue of chicken bursa of Fabricius; both are crucial sites for preimmune B-cell repertoire diversification. Here, we report that appendix regulates precursor lymphocyte recruitment for further development by modulating the sites of extravasation. The total area of peripheral node addressin-positive (PNAd
+) high endothelial venules (HEVs) increased from 1 day to 1 week after birth, remained constant up to 2 weeks and declined to a low and persistent amount by 3 weeks. In normal 1-week and manipulated 5-week appendix where growth of follicles was retarded, PNAd
+ HEVs were present in the basolateral sides of B-cell follicles whereas, in normal 5-wk-appendix these were restricted to T-cell areas. The PNAd was expressed on the lumenal surface of HEVs. The proportions of CD62L
+ B cells in appendix declined from ∼40% at 3 days to 2–3% at 4 weeks. In lymphocyte transfer experiments, CD62L
+ B cells were preferentially recruited compared with CD62L
− B cells, anti-PNAd antibody blocked migration of B cells by ∼50%, and 100 times more B cells were recruited in 1-week compared to 6-week appendix. Thus, a unique spatiotemporal expression pattern of PNAd
+ HEVs is associated with development of B-cell follicles. This regulates migration of blood-borne B-lymphocytes into developing appendix by interacting with CD62L.</description><subject>animal age</subject><subject>animal proteins</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Antigens, Surface - immunology</subject><subject>Appendix</subject><subject>Appendix - immunology</subject><subject>B lymphocyte recruitment</subject><subject>B-lymphocyte migration</subject><subject>B-lymphocytes</subject><subject>B-Lymphocytes - immunology</subject><subject>Cell Movement - immunology</subject><subject>endothelium</subject><subject>Flow Cytometry</subject><subject>food animals</subject><subject>gene expression</subject><subject>genes</subject><subject>immune system</subject><subject>immunoglobulins</subject><subject>Immunohistochemistry</subject><subject>l-Selectin</subject><subject>L-Selectin - immunology</subject><subject>Lymphatic Vessels - immunology</subject><subject>Membrane Proteins - immunology</subject><subject>neonatal development</subject><subject>neonates</subject><subject>perifpheral node addressin-positive high endothelial venules</subject><subject>PNAd</subject><subject>rabbits</subject><subject>Rabbits - immunology</subject><subject>small intestine</subject><subject>temporal variation</subject><issn>0165-2427</issn><issn>1873-2534</issn><issn>1365-2567</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-O0zAQhyMEYsvCGyDwiVvK2I3t5oLErvgnrYQE7Nly7EnrKrGD7UTbl-FZcWklbnCZOcw3P439VdVLCmsKVLw9rBfMbhzXDICvoV0DtI-qFd3KTc34pnlcrQrGa9YweVU9S-kABWy326fVFRWsaWEjVtWvb7ibB53REnyYIqbkgiehJxNGN-0x6oH4YJFoa_9MfT2F5LJbkOzdbk_Q25D3OLgCLujnARMxwecYhkQSonV-d8q7IcNxnPbBHHMhnM-BWFxwCNMJ8Bi8ziUi6q5zmehpKsHu4Xn1pNdDwheXfl3df_zw4_Zzfff105fb93e1aSjPtQVhjGG87yVnoulEJyVtURiQYLRumdVU0C1syxxYDx0vz2k5Fy1D3rB-c129OedOMfycMWU1umRwGHS5bE5KSMEFbZr_glRS4BJEAZszaGJIKWKvpuhGHY-KgjoJVAd1FqhOAhW0qggsa68u-XM3ov27dDFWgNdnoNdB6V10Sd1_Z0A3QGkpkhbi3ZnA8mGLw6iScehNURHRZGWD-_cNvwEeeLwO</recordid><startdate>20060315</startdate><enddate>20060315</enddate><creator>Sinha, Rajesh K.</creator><creator>Alexander, Cornelius</creator><creator>Mage, Rose G.</creator><general>Elsevier B.V</general><scope>FBQ</scope><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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20060315</creationdate><title>Regulated expression of peripheral node addressin-positive high endothelial venules controls seeding of B lymphocytes into developing neonatal rabbit appendix</title><author>Sinha, Rajesh K. ; Alexander, Cornelius ; Mage, Rose G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-d06ccc25ff75264b6b7719e6c070caa92da161808f7502f0b5add955692e542f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>animal age</topic><topic>animal proteins</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Antigens, Surface - immunology</topic><topic>Appendix</topic><topic>Appendix - immunology</topic><topic>B lymphocyte recruitment</topic><topic>B-lymphocyte migration</topic><topic>B-lymphocytes</topic><topic>B-Lymphocytes - immunology</topic><topic>Cell Movement - immunology</topic><topic>endothelium</topic><topic>Flow Cytometry</topic><topic>food animals</topic><topic>gene expression</topic><topic>genes</topic><topic>immune system</topic><topic>immunoglobulins</topic><topic>Immunohistochemistry</topic><topic>l-Selectin</topic><topic>L-Selectin - immunology</topic><topic>Lymphatic Vessels - immunology</topic><topic>Membrane Proteins - immunology</topic><topic>neonatal development</topic><topic>neonates</topic><topic>perifpheral node addressin-positive high endothelial venules</topic><topic>PNAd</topic><topic>rabbits</topic><topic>Rabbits - immunology</topic><topic>small intestine</topic><topic>temporal variation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sinha, Rajesh K.</creatorcontrib><creatorcontrib>Alexander, Cornelius</creatorcontrib><creatorcontrib>Mage, Rose G.</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Veterinary Immunology and Immunopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sinha, Rajesh K.</au><au>Alexander, Cornelius</au><au>Mage, Rose G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulated expression of peripheral node addressin-positive high endothelial venules controls seeding of B lymphocytes into developing neonatal rabbit appendix</atitle><jtitle>Veterinary Immunology and Immunopathology</jtitle><addtitle>Vet Immunol Immunopathol</addtitle><date>2006-03-15</date><risdate>2006</risdate><volume>110</volume><issue>1</issue><spage>97</spage><epage>108</epage><pages>97-108</pages><issn>0165-2427</issn><eissn>1873-2534</eissn><eissn>1365-2567</eissn><abstract>Young rabbit appendix is a homologue of chicken bursa of Fabricius; both are crucial sites for preimmune B-cell repertoire diversification. Here, we report that appendix regulates precursor lymphocyte recruitment for further development by modulating the sites of extravasation. The total area of peripheral node addressin-positive (PNAd
+) high endothelial venules (HEVs) increased from 1 day to 1 week after birth, remained constant up to 2 weeks and declined to a low and persistent amount by 3 weeks. In normal 1-week and manipulated 5-week appendix where growth of follicles was retarded, PNAd
+ HEVs were present in the basolateral sides of B-cell follicles whereas, in normal 5-wk-appendix these were restricted to T-cell areas. The PNAd was expressed on the lumenal surface of HEVs. The proportions of CD62L
+ B cells in appendix declined from ∼40% at 3 days to 2–3% at 4 weeks. In lymphocyte transfer experiments, CD62L
+ B cells were preferentially recruited compared with CD62L
− B cells, anti-PNAd antibody blocked migration of B cells by ∼50%, and 100 times more B cells were recruited in 1-week compared to 6-week appendix. Thus, a unique spatiotemporal expression pattern of PNAd
+ HEVs is associated with development of B-cell follicles. This regulates migration of blood-borne B-lymphocytes into developing appendix by interacting with CD62L.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>16249036</pmid><doi>10.1016/j.vetimm.2005.09.009</doi><tpages>12</tpages></addata></record> |
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subjects | animal age animal proteins Animals Animals, Newborn Antigens, Surface - immunology Appendix Appendix - immunology B lymphocyte recruitment B-lymphocyte migration B-lymphocytes B-Lymphocytes - immunology Cell Movement - immunology endothelium Flow Cytometry food animals gene expression genes immune system immunoglobulins Immunohistochemistry l-Selectin L-Selectin - immunology Lymphatic Vessels - immunology Membrane Proteins - immunology neonatal development neonates perifpheral node addressin-positive high endothelial venules PNAd rabbits Rabbits - immunology small intestine temporal variation |
title | Regulated expression of peripheral node addressin-positive high endothelial venules controls seeding of B lymphocytes into developing neonatal rabbit appendix |
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