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The order of immunoglobulin light chain κ and λ usage in primary and secondary lymphoid tissues of germ-free and conventional piglets

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    0556044 - MBÚ 2022 RIV GB eng J - Journal Article
    Štěpánová, Kateřina - Šinkorová, Jana - Šrůtková, Dagmar - Šinkora jr., Marek - Šinkora, Šimon - Šplíchal, Igor - Šplíchalová, Alla - Butler, J. E. - Šinkora, Marek
    The order of immunoglobulin light chain κ and λ usage in primary and secondary lymphoid tissues of germ-free and conventional piglets.
    Developmental and Comparative Immunology. Roč. 131, June 2022 (2022), č. článku 104392. ISSN 0145-305X. E-ISSN 1879-0089
    R&D Projects: GA ČR(CZ) GA19-01504S
    Institutional support: RVO:61388971
    Keywords : B cell development * B cell receptors * Immunoglobulin light chains * Immunoglobulin rearrangement * Lymphocyte differentiation * Porcine immune system
    OECD category: Zoology
    Impact factor: 2.9, year: 2022
    Method of publishing: Limited access
    https://www.sciencedirect.com/science/article/pii/S0145305X22000544?via%3Dihub

    In pigs (Sus scrofa), the initial immunoglobulin rearrangement of the κ light chain is replaced by λ before the heavy chains rearrange, and the light chains may rearrange even later. This study investigates whether these developmental differences are reflected in the usage of IGK and IGL genes. We found large differences between peripheral B cells and those developing in the bone marrow, and between B cells in germ-free piglets and conventional pigs. During early B cell development in the bone marrow, more 3′ V and 5′ J gene segments for both light chains are used. However, in the peripheral naive repertoire, more 5′ IGLV and 3′ IGLJ genes are used. A similar shift toward the use of more 5′ IGKV and 3′ IGKJ genes is observed later after antigen exposure in conventional pigs. The expression profile showed that most λ+ B cells are generated earlier, while κ+ B cells develop from late precursors that already contain the λ rearrangement. The initial λ rearrangement is retained in both λ+ and κ+ B lymphocytes, and multiple λ transcripts can be found in individual cells. The overall pool of the IGLV repertoire is therefore much larger and more diversified than for IGKV. The κ repertoire is further restricted to the preferential use of only two major IGKV genes, reflecting the limitation for only two consecutive rearrangements. Tracing of silenced λ transcripts in κ+ B cells further confirmed the unconventional mechanism of differential rearrangements in pigs. Our results underline the diversity of the immune system among mammals.
    Permanent Link: http://hdl.handle.net/11104/0330418

     
     
Number of the records: 1  

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