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A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease
iNKT cells play important roles in immune regulation by bridging the innate and acquired immune systems. The functions of iNKT cells have been investigated in mice lacking the Traj18 gene segment that were generated by traditional embryonic stem cell technology, but these animals contain a biased T...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630609/ https://www.ncbi.nlm.nih.gov/pubmed/28986544 http://dx.doi.org/10.1038/s41598-017-12475-4 |
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author | Ren, Yue Sekine-Kondo, Etsuko Shibata, Risa Kato-Itoh, Megumi Umino, Ayumi Yanagida, Ayaka Satoh, Masashi Inoue, Komaki Yamaguchi, Tomoyuki Mochida, Keiichi Nakae, Susumu Van Kaer, Luc Iwabuchi, Kazuya Nakauchi, Hiromitsu Watarai, Hiroshi |
author_facet | Ren, Yue Sekine-Kondo, Etsuko Shibata, Risa Kato-Itoh, Megumi Umino, Ayumi Yanagida, Ayaka Satoh, Masashi Inoue, Komaki Yamaguchi, Tomoyuki Mochida, Keiichi Nakae, Susumu Van Kaer, Luc Iwabuchi, Kazuya Nakauchi, Hiromitsu Watarai, Hiroshi |
author_sort | Ren, Yue |
collection | PubMed |
description | iNKT cells play important roles in immune regulation by bridging the innate and acquired immune systems. The functions of iNKT cells have been investigated in mice lacking the Traj18 gene segment that were generated by traditional embryonic stem cell technology, but these animals contain a biased T cell receptor (TCR) repertoire that might affect immune responses. To circumvent this confounding factor, we have generated a new strain of iNKT cell-deficient mice by deleting the Traj18 locus using CRISPR/Cas9 technology, and these animals contain an unbiased TCR repertoire. We employed these mice to investigate the contribution of iNKT cells to metabolic disease and found a pathogenic role of these cells in obesity-associated insulin-resistance. The new Traj18-deficient mouse strain will assist in studies of iNKT cell biology. |
format | Online Article Text |
id | pubmed-5630609 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56306092017-10-17 A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease Ren, Yue Sekine-Kondo, Etsuko Shibata, Risa Kato-Itoh, Megumi Umino, Ayumi Yanagida, Ayaka Satoh, Masashi Inoue, Komaki Yamaguchi, Tomoyuki Mochida, Keiichi Nakae, Susumu Van Kaer, Luc Iwabuchi, Kazuya Nakauchi, Hiromitsu Watarai, Hiroshi Sci Rep Article iNKT cells play important roles in immune regulation by bridging the innate and acquired immune systems. The functions of iNKT cells have been investigated in mice lacking the Traj18 gene segment that were generated by traditional embryonic stem cell technology, but these animals contain a biased T cell receptor (TCR) repertoire that might affect immune responses. To circumvent this confounding factor, we have generated a new strain of iNKT cell-deficient mice by deleting the Traj18 locus using CRISPR/Cas9 technology, and these animals contain an unbiased TCR repertoire. We employed these mice to investigate the contribution of iNKT cells to metabolic disease and found a pathogenic role of these cells in obesity-associated insulin-resistance. The new Traj18-deficient mouse strain will assist in studies of iNKT cell biology. Nature Publishing Group UK 2017-10-06 /pmc/articles/PMC5630609/ /pubmed/28986544 http://dx.doi.org/10.1038/s41598-017-12475-4 Text en © The Author(s) 2017 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 Ren, Yue Sekine-Kondo, Etsuko Shibata, Risa Kato-Itoh, Megumi Umino, Ayumi Yanagida, Ayaka Satoh, Masashi Inoue, Komaki Yamaguchi, Tomoyuki Mochida, Keiichi Nakae, Susumu Van Kaer, Luc Iwabuchi, Kazuya Nakauchi, Hiromitsu Watarai, Hiroshi A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title | A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title_full | A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title_fullStr | A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title_full_unstemmed | A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title_short | A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease |
title_sort | novel mouse model of inkt cell-deficiency generated by crispr/cas9 reveals a pathogenic role of inkt cells in metabolic disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630609/ https://www.ncbi.nlm.nih.gov/pubmed/28986544 http://dx.doi.org/10.1038/s41598-017-12475-4 |
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