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鼠肠道上皮内淋巴细胞中Qa-2依赖性的CD8α/α T细胞受体α/β(+)细胞选择

Qa-2-dependent selection of CD8alpha/alpha T cell receptor alpha/beta(+) cells in murine intestinal intraepithelial lymphocytes.

作者信息

Das G, Gould D S, Augustine M M, Fragoso G, Sciutto E, Stroynowski I, Van Kaer L, Schust D J, Ploegh H, Janeway C A

机构信息

Section of Immunobiology, Yale University School of Medicine, and the Howard Hughes Medical Institute, New Haven, Connecticut 06520-8011, USA.

出版信息

J Exp Med. 2000 Nov 20;192(10):1521-8. doi: 10.1084/jem.192.10.1521.

DOI:10.1084/jem.192.10.1521
PMID:11085754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2193183/
Abstract

Murine intestinal intraepithelial lymphocytes (iIELs) are made up of a heterogeneous mix of T cells with unique phenotypes. Whereas CD8(+) T cells in peripheral lymphoid organs use CD8alpha/beta and are selected on MHC class Ia molecules, a majority of iIELs use CD8alpha/alpha. Here, we report that the presence of CD8alpha/alpha TCR-alpha/beta cells in iIELs is independent of classical MHC class I molecules K(b) and D(b), as illustrated by their presence in K(b)/D(b) double-knockout mice and in mice lacking a nonclassical MHC class I molecule, CD1d. Most strikingly, their presence is decreased by approximately 70% in mice lacking transporter associated with antigen processing (TAP). The TAP-dependent nonclassical MHC class I molecule Qa-2 is strongly implicated in the presence of these cells, as inferred from the low numbers of CD8alpha/alpha TCR-alpha/beta T cells in mice deficient in Qa-2 genes. Second, a Qa-2-transgenic mouse made in a Qa-2(-) strain showed an increase in the numbers of CD8alpha/alpha cells among its iIELs. Thus, the presence of CD8alpha/alpha TCR-alpha/beta cells in iIELs is mainly dependent on the nonclassical MHC class I molecule Qa-2.

摘要

小鼠肠道上皮内淋巴细胞(iIELs)由具有独特表型的T细胞异质性混合组成。在外周淋巴器官中,CD8(+) T细胞使用CD8α/β,并在MHC I类分子上进行选择,而大多数iIELs使用CD8α/α。在此,我们报告iIELs中CD8α/α TCR-α/β细胞的存在独立于经典MHC I类分子K(b)和D(b),这在K(b)/D(b)双敲除小鼠以及缺乏非经典MHC I类分子CD1d的小鼠中得到了证明。最引人注目的是,在缺乏与抗原加工相关转运体(TAP)的小鼠中,它们的存在减少了约70%。从Qa-2基因缺陷小鼠中CD8α/α TCR-α/β T细胞数量较少可以推断,TAP依赖的非经典MHC I类分子Qa-2与这些细胞的存在密切相关。其次,在Qa-2(-)品系中构建的Qa-2转基因小鼠,其iIELs中CD8α/α细胞数量增加。因此,iIELs中CD8α/α TCR-α/β细胞的存在主要依赖于非经典MHC I类分子Qa-2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/d58427873393/JEM000524.f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/c0abfef79395/JEM000524.f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/64b4c1502724/JEM000524.f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/32c33857dd24/JEM000524.f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/d58427873393/JEM000524.f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/c0abfef79395/JEM000524.f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/64b4c1502724/JEM000524.f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/32c33857dd24/JEM000524.f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3130/2193183/d58427873393/JEM000524.f4.jpg

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