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迁移至小鼠小肠上皮层的CD4⁺T细胞受体αβ⁺T细胞中CD8α的共表达。

Co-expression of CD8 alpha in CD4+ T cell receptor alpha beta + T cells migrating into the murine small intestine epithelial layer.

作者信息

Reimann J, Rudolphi A

机构信息

Institute for Medical Microbiology and Immunology, University of Ulm, Germany.

出版信息

Eur J Immunol. 1995 Jun;25(6):1580-8. doi: 10.1002/eji.1830250617.

Abstract

We investigated the surface phenotype of CD3+CD4+ T cell receptor (TCR) alpha beta + T cells repopulating the intestinal lymphoid tissues of C.B-17 scid/scid (severe-combined immunodeficient; scid) (H-2d, Ld+) mice. CD4+ CD8- T cells were cell sorter-purified from various secondary and tertiary lymphoid organs of congenic C.B-17 +/+ (H-2d, Ld+) or semi-syngeneic dm2 (H-2d, Ld-) immunocompetent donor mice. After transfer of 10(5) cells into young scid mice, a mucosa-homing, memory CD44hi CD45RBlo CD4+ T cell population was selectively engrafted. Large numbers of single-positive (SP) CD3+ CD2+ CD28+ CD4+ CD8- T cells that expressed the alpha 4 integrin chain CD49d were found in the spleen, the mesenteric lymph nodes, the peritoneal cavity and the gut lamina propria of transplanted scid mice. Unexpectedly, large populations of donor-type double-positive (DP) CD4+ CD8 alpha + CD8 beta - T cells with high expression of the CD3/TCR complex appeared in the epithelial layer of the small intestine of transplanted scid mice. In contrast to SP CD4+ T cells, the intraepithelial DP T cells showed low expression of the CD2 and the CD28 co-stimulator molecules, and of the alpha 4 integrin chain CD49d, but expressed high levels of the alpha IEL integrin chain CD103. The TCR-V beta repertoire of DP but not SP intraepithelial CD4+ T cells was biased towards usage of the V beta 6 and V beta 8 viable domains. Highly purified populations of SP and DP CD4+ T cell populations from the small intestine epithelial layer of transplanted scid mice had different abilities to repopulate secondary scid recipient mice: SP CD4+ T cells repopulated various lymphoid tissues of the immunodeficient host, while intraepithelial DP CD4+ T cells did not. Hence, a subset of CD3+ CD4+ TCR alpha beta + T cells apparently undergoes striking phenotypic changes when it enters the microenvironment of the small intestine epithelial layer.

摘要

我们研究了重新填充C.B-17 scid/scid(严重联合免疫缺陷;scid)(H-2d,Ld+)小鼠肠道淋巴组织的CD3+CD4+T细胞受体(TCR)αβ+T细胞的表面表型。从同基因C.B-17 +/+(H-2d,Ld+)或半同基因dm2(H-2d,Ld-)免疫 competent供体小鼠的各种二级和三级淋巴器官中通过细胞分选纯化CD4+CD8-T细胞。将10(5)个细胞转移到年轻的scid小鼠体内后,一个归巢于黏膜的记忆性CD44hi CD45RBlo CD4+T细胞群体被选择性植入。在移植的scid小鼠的脾脏、肠系膜淋巴结、腹腔和肠固有层中发现了大量表达α4整合素链CD49d的单阳性(SP)CD3+CD2+CD28+CD4+CD8-T细胞。出乎意料的是,在移植的scid小鼠小肠上皮层中出现了大量高表达CD3/TCR复合物的供体型双阳性(DP)CD4+CD8α+CD8β-T细胞。与SP CD4+T细胞相比,上皮内DP T细胞的CD2和CD28共刺激分子以及α4整合素链CD49d表达较低,但αIEL整合素链CD103表达水平较高。DP上皮内CD4+T细胞而非SP上皮内CD4+T细胞的TCR-Vβ库偏向于使用Vβ6和Vβ8可变区。从移植的scid小鼠小肠上皮层中高度纯化的SP和DP CD4+T细胞群体在重新填充二级scid受体小鼠方面具有不同的能力:SP CD4+T细胞重新填充免疫缺陷宿主的各种淋巴组织,而上皮内DP CD4+T细胞则不能。因此,当CD3+CD4+TCRαβ+T细胞的一个亚群进入小肠上皮层的微环境时,显然会发生显著表型变化。

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