CD1d-expressing Dendritic Cells but Not Thymic Epithelial Cells Can Mediate Negative Selection of NKT Cells

Author:

Chun Taehoon12,Page Michael J.3,Gapin Laurent4,Matsuda Jennifer L.4,Xu Honglin12,Nguyen Hanh12,Kang Hyung-Sik2,Stanic Aleksandar K.5,Joyce Sebastian5,Koltun Walter A.3,Chorney Michael J.3,Kronenberg Mitchell4,Wang Chyung-Ru12

Affiliation:

1. Gwen Knapp Center for Lupus and Immunology Research, University of Chicago, Chicago, IL 60637

2. Committee on Immunology and Department of Pathology, University of Chicago, Chicago, IL 60637

3. Department of Surgery, Pennsylvania State University College of Medicine, Hershey, PA 17033

4. La Jolla Institute for Allergy and Immunology, San Diego, CA 92121

5. Department of Microbiology and Immunology, Vanderbilt University, School of Medicine, Nashville, TN 37232

Abstract

Natural killer T (NKT) cells are a unique immunoregulatory T cell population that is positively selected by CD1d-expressing thymocytes. Previous studies have shown that NKT cells exhibit autoreactivity, which raises the question of whether they are subject to negative selection. Here, we report that the addition of agonist glycolipid α-galactosylceramide (α-GalCer) to a fetal thymic organ culture (FTOC) induces a dose-dependent disappearance of NKT cells, suggesting that NKT cells are susceptible to negative selection. Overexpression of CD1d in transgenic (Tg) mice results in reduced numbers of NKT cells, and the residual NKT cells in CD1d-Tg mice exhibit both an altered Vβ usage and a reduced sensitivity to antigen. Furthermore, bone marrow (BM) chimeras between Tg and WT mice reveal that CD1d-expressing BM-derived dendritic cells, but not thymic epithelial cells, mediate the efficient negative selection of NKT cells. Thus, our data suggest that NKT cells developmentally undergo negative selection when engaged by high-avidity antigen or abundant self-antigen.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Cited by 119 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3