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The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation
Lymphocytes are some of the most motile cells of vertebrates, constantly navigating through various organ systems. Their specific positioning in the body is delicately controlled by site-specific directional cues such as chemokines. While it has long been suspected that an intrinsic molecular pilot,...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170861/ https://www.ncbi.nlm.nih.gov/pubmed/32313148 http://dx.doi.org/10.1038/s41598-020-63629-w |
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author | Sun, Honghong Lin, Mei Zamani, Ali Goldsmith, Jason R. Boggs, Amanda E. Li, Mingyue Lee, Chin-Nien Chen, Xu Li, Xinyuan Li, Ting Dorrity, Brigid L. Li, Ning Lou, Yunwei Shi, Songlin Wang, Wei Chen, Youhai H. |
author_facet | Sun, Honghong Lin, Mei Zamani, Ali Goldsmith, Jason R. Boggs, Amanda E. Li, Mingyue Lee, Chin-Nien Chen, Xu Li, Xinyuan Li, Ting Dorrity, Brigid L. Li, Ning Lou, Yunwei Shi, Songlin Wang, Wei Chen, Youhai H. |
author_sort | Sun, Honghong |
collection | PubMed |
description | Lymphocytes are some of the most motile cells of vertebrates, constantly navigating through various organ systems. Their specific positioning in the body is delicately controlled by site-specific directional cues such as chemokines. While it has long been suspected that an intrinsic molecular pilot, akin to a ship’s pilot, guides lymphocyte navigation, the nature of this pilot is unknown. Here we show that the TIPE (TNF-α-induced protein 8-like) family of proteins pilot lymphocytes by steering them toward chemokines. TIPE proteins are carriers of lipid second messengers. They mediate chemokine-induced local generation of phosphoinositide second messengers, but inhibit global activation of the small GTPase Rac. TIPE-deficient T lymphocytes are completely pilot-less: they are unable to migrate toward chemokines despite their normal ability to move randomly. As a consequence, TIPE-deficient mice have a marked defect in positioning their T lymphocytes to various tissues, both at the steady-state and during inflammation. Thus, TIPE proteins pilot lymphocytes during migration and may be targeted for the treatment of lymphocyte-related disorders. |
format | Online Article Text |
id | pubmed-7170861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71708612020-04-23 The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation Sun, Honghong Lin, Mei Zamani, Ali Goldsmith, Jason R. Boggs, Amanda E. Li, Mingyue Lee, Chin-Nien Chen, Xu Li, Xinyuan Li, Ting Dorrity, Brigid L. Li, Ning Lou, Yunwei Shi, Songlin Wang, Wei Chen, Youhai H. Sci Rep Article Lymphocytes are some of the most motile cells of vertebrates, constantly navigating through various organ systems. Their specific positioning in the body is delicately controlled by site-specific directional cues such as chemokines. While it has long been suspected that an intrinsic molecular pilot, akin to a ship’s pilot, guides lymphocyte navigation, the nature of this pilot is unknown. Here we show that the TIPE (TNF-α-induced protein 8-like) family of proteins pilot lymphocytes by steering them toward chemokines. TIPE proteins are carriers of lipid second messengers. They mediate chemokine-induced local generation of phosphoinositide second messengers, but inhibit global activation of the small GTPase Rac. TIPE-deficient T lymphocytes are completely pilot-less: they are unable to migrate toward chemokines despite their normal ability to move randomly. As a consequence, TIPE-deficient mice have a marked defect in positioning their T lymphocytes to various tissues, both at the steady-state and during inflammation. Thus, TIPE proteins pilot lymphocytes during migration and may be targeted for the treatment of lymphocyte-related disorders. Nature Publishing Group UK 2020-04-20 /pmc/articles/PMC7170861/ /pubmed/32313148 http://dx.doi.org/10.1038/s41598-020-63629-w Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sun, Honghong Lin, Mei Zamani, Ali Goldsmith, Jason R. Boggs, Amanda E. Li, Mingyue Lee, Chin-Nien Chen, Xu Li, Xinyuan Li, Ting Dorrity, Brigid L. Li, Ning Lou, Yunwei Shi, Songlin Wang, Wei Chen, Youhai H. The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title | The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title_full | The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title_fullStr | The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title_full_unstemmed | The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title_short | The TIPE Molecular Pilot That Directs Lymphocyte Migration in Health and Inflammation |
title_sort | tipe molecular pilot that directs lymphocyte migration in health and inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7170861/ https://www.ncbi.nlm.nih.gov/pubmed/32313148 http://dx.doi.org/10.1038/s41598-020-63629-w |
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