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Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1
LST1 is a small adaptor protein expressed in leukocytes of myeloid lineage. Due to the binding to protein tyrosine phosphatases SHP1 and SHP2 it was thought to have negative regulatory function in leukocyte signaling. It was also shown to be involved in cytoskeleton regulation and generation of tunn...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111073/ https://www.ncbi.nlm.nih.gov/pubmed/33986741 http://dx.doi.org/10.3389/fimmu.2021.618332 |
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author | Fabisik, Matej Tureckova, Jolana Pavliuchenko, Nataliia Kralova, Jarmila Balounova, Jana Vicikova, Kristina Skopcova, Tereza Spoutil, Frantisek Pokorna, Jana Angelisova, Pavla Malissen, Bernard Prochazka, Jan Sedlacek, Radislav Brdicka, Tomas |
author_facet | Fabisik, Matej Tureckova, Jolana Pavliuchenko, Nataliia Kralova, Jarmila Balounova, Jana Vicikova, Kristina Skopcova, Tereza Spoutil, Frantisek Pokorna, Jana Angelisova, Pavla Malissen, Bernard Prochazka, Jan Sedlacek, Radislav Brdicka, Tomas |
author_sort | Fabisik, Matej |
collection | PubMed |
description | LST1 is a small adaptor protein expressed in leukocytes of myeloid lineage. Due to the binding to protein tyrosine phosphatases SHP1 and SHP2 it was thought to have negative regulatory function in leukocyte signaling. It was also shown to be involved in cytoskeleton regulation and generation of tunneling nanotubes. LST1 gene is located in MHCIII locus close to many immunologically relevant genes. In addition, its expression increases under inflammatory conditions such as viral infection, rheumatoid arthritis and inflammatory bowel disease and its deficiency was shown to result in slightly increased sensitivity to influenza infection in mice. However, little else is known about its role in the immune system homeostasis and immune response. Here we show that similar to humans, LST1 is expressed in mice in the cells of the myeloid lineage. In vivo, its deficiency results in alterations in multiple leukocyte subset abundance in steady state and under inflammatory conditions. Moreover, LST1-deficient mice show significant level of resistance to dextran sodium sulphate (DSS) induced acute colitis, a model of inflammatory bowel disease. These data demonstrate that LST1 regulates leukocyte abundance in lymphoid organs and inflammatory response in the gut. |
format | Online Article Text |
id | pubmed-8111073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81110732021-05-12 Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 Fabisik, Matej Tureckova, Jolana Pavliuchenko, Nataliia Kralova, Jarmila Balounova, Jana Vicikova, Kristina Skopcova, Tereza Spoutil, Frantisek Pokorna, Jana Angelisova, Pavla Malissen, Bernard Prochazka, Jan Sedlacek, Radislav Brdicka, Tomas Front Immunol Immunology LST1 is a small adaptor protein expressed in leukocytes of myeloid lineage. Due to the binding to protein tyrosine phosphatases SHP1 and SHP2 it was thought to have negative regulatory function in leukocyte signaling. It was also shown to be involved in cytoskeleton regulation and generation of tunneling nanotubes. LST1 gene is located in MHCIII locus close to many immunologically relevant genes. In addition, its expression increases under inflammatory conditions such as viral infection, rheumatoid arthritis and inflammatory bowel disease and its deficiency was shown to result in slightly increased sensitivity to influenza infection in mice. However, little else is known about its role in the immune system homeostasis and immune response. Here we show that similar to humans, LST1 is expressed in mice in the cells of the myeloid lineage. In vivo, its deficiency results in alterations in multiple leukocyte subset abundance in steady state and under inflammatory conditions. Moreover, LST1-deficient mice show significant level of resistance to dextran sodium sulphate (DSS) induced acute colitis, a model of inflammatory bowel disease. These data demonstrate that LST1 regulates leukocyte abundance in lymphoid organs and inflammatory response in the gut. Frontiers Media S.A. 2021-04-27 /pmc/articles/PMC8111073/ /pubmed/33986741 http://dx.doi.org/10.3389/fimmu.2021.618332 Text en Copyright © 2021 Fabisik, Tureckova, Pavliuchenko, Kralova, Balounova, Vicikova, Skopcova, Spoutil, Pokorna, Angelisova, Malissen, Prochazka, Sedlacek and Brdicka https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Fabisik, Matej Tureckova, Jolana Pavliuchenko, Nataliia Kralova, Jarmila Balounova, Jana Vicikova, Kristina Skopcova, Tereza Spoutil, Frantisek Pokorna, Jana Angelisova, Pavla Malissen, Bernard Prochazka, Jan Sedlacek, Radislav Brdicka, Tomas Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title | Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title_full | Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title_fullStr | Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title_full_unstemmed | Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title_short | Regulation of Inflammatory Response by Transmembrane Adaptor Protein LST1 |
title_sort | regulation of inflammatory response by transmembrane adaptor protein lst1 |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111073/ https://www.ncbi.nlm.nih.gov/pubmed/33986741 http://dx.doi.org/10.3389/fimmu.2021.618332 |
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