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CRISPR/Cas9 技术构建的 iNKT 细胞缺陷型小鼠模型揭示了 iNKT 细胞在代谢性疾病中的致病作用

A Novel Mouse Model of iNKT Cell-deficiency Generated by CRISPR/Cas9 Reveals a Pathogenic Role of iNKT Cells in Metabolic Disease.

机构信息

Division of Stem Cell Cellomics, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo, Japan.

The Neurological Institute of Jiangxi Province, Department of Neurology, Jiangxi Provincial People's Hospital, Nanchang, Jiangxi, China.

出版信息

Sci Rep. 2017 Oct 6;7(1):12765. doi: 10.1038/s41598-017-12475-4.

Abstract

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.

摘要

iNKT 细胞在连接先天免疫和获得性免疫系统方面发挥着重要作用,调节免疫功能。传统的胚胎干细胞技术缺失 Traj18 基因片段的小鼠中已经对 iNKT 细胞的功能进行了研究,但这些动物的 T 细胞受体(TCR) repertoire 存在偏向性,可能会影响免疫反应。为了避免这种混杂因素,我们利用 CRISPR/Cas9 技术删除 Traj18 基因座,产生了一种新型的 iNKT 细胞缺陷小鼠,这些动物的 TCR repertoire 没有偏向性。我们利用这些小鼠来研究 iNKT 细胞对代谢疾病的贡献,发现这些细胞在肥胖相关胰岛素抵抗中具有致病性作用。新型的 Traj18 缺陷小鼠品系将有助于 iNKT 细胞生物学的研究。

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