Speculation on the lineage relationships among CD4(-)8(+) gut-derived T cells and their role(s).

Speculation on the lineage relationships among CD4(-)8(+) gut-derived T cells and their role(s).
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推测 CD4(-)8( ) 肠道来源的 T 细胞之间的谱系关系及其作用。

DOI:
--
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发表时间:
1999
影响因子:
7.8
通讯作者:
M. Julius
M. Julius
中科院分区:
医学2区
文献类型:
--
作者:
P. Poussier;M. Julius

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小鼠肠粘膜的胸腺非依赖性T淋巴细胞生成能力已经建立。Cryptopatches现在已经被确定为肠道衍生T细胞的难以捉摸的前体的位置。这些隐补丁细胞已显示产生表达TCR γ δ或TCR α的肠T细胞。在这里,我们讨论的作用,MHC的发展和选择肠源性T细胞。通过对表达转基因TCR α的动物中iIEL选择的分析,在存在或不存在p56(lck)的情况下,我们讨论了CD 4(-)8(+)iIEL亚群之间的谱系关系及其可能的功能。
The thymus-independent T lymphopoietic capacity of the murine intestinal mucosa has been established. Cryptopatches have now been identified as the location of the elusive precursors for gut-derived T cells. These cryptopatch cells have been shown to give rise to intestinal T cells expressing either TCRgammadelta or TCRalphabeta. Here we discuss the role of MHC in the development and selection of gut-derived T cells. Through the analysis of iIEL selection in animals expressing a transgenic TCRalphabeta, in the presence or absence of p56(lck), we discuss lineage relationships among CD4(-)8(+) iIEL subsets, and their possible function(s).
无胸腺放射嵌合体中表达膜 T 细胞受体的骨髓来源肠上皮 T 细胞的分化和功能成熟。
DOI: --
发表时间: 1990
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者:
Mosley,RL;Styre,D;Klein,JR
通讯作者: Klein,JR
DOI: 10.1016/1074-7613(94)90038-8
发表时间: 1994-11-01
期刊: IMMUNITY
影响因子: 32.4
作者:
VANOERS, NSC;KILLEEN, N;WEISS, A
通讯作者: WEISS, A