Egyszerű nézet

dc.contributor.author Nagy, Nándor
dc.contributor.author Busalt, Florian
dc.contributor.author Halasy, Viktória
dc.contributor.author Kohn, Marina
dc.contributor.author Schmieder, Stefan
dc.contributor.author Fejszák, Nóra
dc.contributor.author Kaspers, Bernd
dc.contributor.author Haertle, Sonja
dc.date.accessioned 2020-09-28T10:00:17Z
dc.date.available 2020-09-28T10:00:17Z
dc.date.issued 2020
dc.identifier 85088794944
dc.identifier.citation journalVolume=11;journalTitle=FRONTIERS IN IMMUNOLOGY;pagination= 1468, pages 18;journalAbbreviatedTitle=FRONT IMMUNOL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/8507
dc.identifier.uri doi:10.3389/fimmu.2020.01468
dc.description.abstract In contrast to mammals, early B cell differentiation and diversification of the antibody repertoire in chickens do not take place in the bone marrow but in a specialized gut associated lymphoid tissue (GALT), the bursa of Fabricius. During embryonic development, B cell precursors migrate to the bursa anlage, where they proliferate and diversify their B cell receptor repertoire. Around hatch these diversified B cells start to emigrate from the bursa of Fabricius and populate peripheral lymphoid organs, but very little is known how the migratory processes are regulated. As CXCL12 (syn. SDF-1) and CXCR4 were shown to be essential for the control of B cell migration during the development of lymphoid tissues in mammals, we analyzed expression and function of this chemokine/chemokine-receptor pair in the chicken bursa. We found a strong variation of mRNA abundance of CXCL12 and CXCR4 in different stages of bursa development, with high abundance of CXCL12 mRNA in the bursa anlage at embryonic day 10 (ED10).In situhybridization demonstrated disseminated CXCL12 expression in the early bursa anlage, which condensed in the developing follicles and was mainly restricted to the follicle cortex post-hatch. Flow cytometric analysis detected CXCR4 protein already on early B cell stages, increasing during bursal development. Post-hatch, a subpopulation with the hallmarks of emigrating B cells became detectable, which had lower CXCR4 expression, suggesting that downregulation of CXCR4 is necessary to leave the CXCL12-high bursal environment.In vivoblockade of CXCR4 using AMD3100 at the time of B cell precursor immigration strongly inhibited follicle development, demonstrating that CXCL12 attracts pre-bursal B cells into the bursal anlage. Altogether, we show that CXCL12 and its receptor CXCR4 are important for both populating the bursa with B cells and emigration of mature B cells into the periphery post hatch, and that CXCR4 function in primary B cell organs is conserved between mammals and birds.
dc.relation.ispartof urn:issn:1664-3224
dc.title In and Out of the Bursa-The Role of CXCR4 in Chicken B Cell Development
dc.type Journal Article
dc.date.updated 2020-09-25T09:37:20Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 31439950
dc.identifier.wos 000556296900001
dc.identifier.scopus 85088794944
dc.identifier.pubmed 32765509
dc.contributor.department SE/AOK/I/Anatómiai, Szövet- és Fejlődéstani Intézet
dc.contributor.institution Semmelweis Egyetem


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