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    <title>The role of CCRL2 in the regulation of germinal centre B-cell migration and a new regulatory step in T-cell migration into tissue during inflammation; separating the wanted from the unwanted</title>
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      <item>RA</item>
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    <abstract>CC-Chemokine receptor like 2 (CCRL2) is the newest member of the atypical chemokine receptor family, a set of proteins which tend to act as “decoy receptors”, causing a chemoattractant gradient of their ligands. Using SYBR-Green and Taqman RT-PCR analysis of murine tissue, this study aimed to characterise the expression of CCRL2 in the spleen, thymus and lymph nodes. Using specifically designed primers, the PCR techniques detected an alternative, “long”, spliced variant of CCRL2 within the thymus. CCRL2 mRNA expression was also defined over 8 days, during the lifetime of the germinal centre. CCRL2 mRNA expression was measured within B cells, the germinal centre or the T Zone. Due to its high expression within plasma B cells at days 4 and 7, CCRL2 may be involved in plasma cell exit from the GC. However, CCRL2 mRNA was also expressed within the germinal centre on days 7 and 8, which may suggest the receptor also has a role in germinal centre breakdown. Finally, this study also started the process of monoclonal antibody production to murine CCRL2. CCRL2 DNA was successfully cloned into a plasmid vector and transformed into E. coli in preparation for transfection into a mammalian cell line

</abstract>
    <date>2011-12</date>
    <date_tp>2011-08</date_tp>
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    <copyright_status>This unpublished thesis/dissertation is copyright of the author and/or third parties.
The intellectual property rights of the author or third parties in respect of this work are as defined by The Copyright Designs and Patents Act 1988 or as modified by any successor legislation.  Any use made of information contained in this thesis/dissertation must be in accordance with that legislation and must be properly acknowledged.
Further distribution or reproduction in any format is prohibited without the permission of the copyright holder.</copyright_status>
    <full_text_status>public</full_text_status>
    <pages>120</pages>
    <institution>University of Birmingham</institution>
    <department>School of Immunity and Infection</department>
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