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Generation and first characterization of TRDC-knockout pigs lacking γδ T cells

The TRDC-locus encodes the T cell receptor delta constant region, one component of the γδ T cell receptor which is essential for development of γδ T cells. In contrast to peptide recognition by αβ T cells, antigens activating γδ T cells are mostly MHC independent and not well characterized. Therefor...

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Autores principales: Petersen, Bjoern, Kammerer, Robert, Frenzel, Antje, Hassel, Petra, Dau, Tung Huy, Becker, Roswitha, Breithaupt, Angele, Ulrich, Reiner Georg, Lucas-Hahn, Andrea, Meyers, Gregor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298467/
https://www.ncbi.nlm.nih.gov/pubmed/34294758
http://dx.doi.org/10.1038/s41598-021-94017-7
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author Petersen, Bjoern
Kammerer, Robert
Frenzel, Antje
Hassel, Petra
Dau, Tung Huy
Becker, Roswitha
Breithaupt, Angele
Ulrich, Reiner Georg
Lucas-Hahn, Andrea
Meyers, Gregor
author_facet Petersen, Bjoern
Kammerer, Robert
Frenzel, Antje
Hassel, Petra
Dau, Tung Huy
Becker, Roswitha
Breithaupt, Angele
Ulrich, Reiner Georg
Lucas-Hahn, Andrea
Meyers, Gregor
author_sort Petersen, Bjoern
collection PubMed
description The TRDC-locus encodes the T cell receptor delta constant region, one component of the γδ T cell receptor which is essential for development of γδ T cells. In contrast to peptide recognition by αβ T cells, antigens activating γδ T cells are mostly MHC independent and not well characterized. Therefore, the function of γδ T cells and their contribution to protection against infections is still unclear. Higher numbers of circulating γδ T cells compared to mice, render the pig a suitable animal model to study γδ T cells. Knocking-out the porcine TRDC-locus by intracytoplasmic microinjection and somatic cell nuclear transfer resulted in healthy living γδ T cell deficient offspring. Flow cytometric analysis revealed that TRDC-KO pigs lack γδ T cells in peripheral blood mononuclear cells (PBMC) and spleen cells. The composition of the remaining leucocyte subpopulations was not affected by the depletion of γδ T cells. Genome-wide transcriptome analyses in PBMC revealed a pattern of changes reflecting the impairment of known or expected γδ T cell dependent pathways. Histopathology did not reveal developmental abnormalities of secondary lymphoid tissues. However, in a vaccination experiment the KO pigs stayed healthy but had a significantly lower neutralizing antibody titer as the syngenic controls.
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spelling pubmed-82984672021-07-23 Generation and first characterization of TRDC-knockout pigs lacking γδ T cells Petersen, Bjoern Kammerer, Robert Frenzel, Antje Hassel, Petra Dau, Tung Huy Becker, Roswitha Breithaupt, Angele Ulrich, Reiner Georg Lucas-Hahn, Andrea Meyers, Gregor Sci Rep Article The TRDC-locus encodes the T cell receptor delta constant region, one component of the γδ T cell receptor which is essential for development of γδ T cells. In contrast to peptide recognition by αβ T cells, antigens activating γδ T cells are mostly MHC independent and not well characterized. Therefore, the function of γδ T cells and their contribution to protection against infections is still unclear. Higher numbers of circulating γδ T cells compared to mice, render the pig a suitable animal model to study γδ T cells. Knocking-out the porcine TRDC-locus by intracytoplasmic microinjection and somatic cell nuclear transfer resulted in healthy living γδ T cell deficient offspring. Flow cytometric analysis revealed that TRDC-KO pigs lack γδ T cells in peripheral blood mononuclear cells (PBMC) and spleen cells. The composition of the remaining leucocyte subpopulations was not affected by the depletion of γδ T cells. Genome-wide transcriptome analyses in PBMC revealed a pattern of changes reflecting the impairment of known or expected γδ T cell dependent pathways. Histopathology did not reveal developmental abnormalities of secondary lymphoid tissues. However, in a vaccination experiment the KO pigs stayed healthy but had a significantly lower neutralizing antibody titer as the syngenic controls. Nature Publishing Group UK 2021-07-22 /pmc/articles/PMC8298467/ /pubmed/34294758 http://dx.doi.org/10.1038/s41598-021-94017-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Petersen, Bjoern
Kammerer, Robert
Frenzel, Antje
Hassel, Petra
Dau, Tung Huy
Becker, Roswitha
Breithaupt, Angele
Ulrich, Reiner Georg
Lucas-Hahn, Andrea
Meyers, Gregor
Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title_full Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title_fullStr Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title_full_unstemmed Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title_short Generation and first characterization of TRDC-knockout pigs lacking γδ T cells
title_sort generation and first characterization of trdc-knockout pigs lacking γδ t cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298467/
https://www.ncbi.nlm.nih.gov/pubmed/34294758
http://dx.doi.org/10.1038/s41598-021-94017-7
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