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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Distinct stage-specific cis-active transcriptional mechanisms control expression of T cell coreceptor CD8 alpha at double- and single-positive stages of thymic development.
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Distinct stage-specific cis-active transcriptional mechanisms control expression of T cell coreceptor CD8 alpha at double- and single-positive stages of thymic development.

机译:不同的阶段特异性顺式活性转录机制控制胸腺发育的双阳性和单阳性阶段T细胞共受体CD8α的表达。

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摘要

Developing thymocytes that give rise to CD8+ (cytotoxic) and CD4+ (helper) alpha beta-TCR T lymphocytes go through progressive stages of expression of coreceptors CD8 and CD4 from being negative for both (the double-negative stage), to coexpressing both (the double-positive (DP) stage), to a mutually exclusive sublineage-specific expression of one or the other (the single-positive (SP) stage). To delineate the mechanisms underlying regulation of CD8 during these developmental transitions, we have examined expression of a series of mouse CD8 alpha gene constructs in developing T cells of conventional and CD8 alpha "knock-out" transgenic mice. Our results indicate that cis-active transcriptional control sequences essential for stage- and sublineage-specific expression lie within a 5' 40-kb segment of the CD8 locus, approximately 12 kb upstream of the CD8 alpha gene. Studies to characterize and sublocalize these cis sequences showed that a 17-kb 5' subfragment is able to direct expression of the CD8 alpha gene up to the CD3intermediate DP stage but not in more mature DP or SP cells. These results indicate that stage-specific expression of CD8 alpha in developing T cells is mediated by the differential activity of multiple functionally distinct cis-active transcriptional control mechanisms. It will be important to determine the relationship of "switching" between these cis mechanisms and selection.
机译:产生CD8 +(细胞毒性)和CD4 +(辅助)αβ-TCRT淋巴细胞的发育中胸腺细胞经历了共受体CD8和CD4的表达从两个阶段均呈阴性(双阴性阶段)到共表达两个阶段(双阳性(DP)阶段),转换为一个或另一个的互斥子系特定表达(单阳性(SP)阶段)。为了描述在这些发育过渡过程中调节CD8的基本机制,我们研究了常规和CD8 alpha“敲除”转基因小鼠的T细胞中一系列小鼠CD8 alpha基因构建体的表达。我们的结果表明,对于阶段和亚谱系特异性表达必不可少的顺式活性转录控制序列位于CD8基因座的5'40-kb片段内,在CD8α基因上游约12 kb。表征和亚定位这些顺式序列的研究表明,一个17-kb的5'亚片段能够指导CD8α基因的表达直至CD3中间DP阶段,但不能在更成熟的DP或SP细胞中进行。这些结果表明,CD8α在发育中的T细胞中的阶段特异性表达是由多种功能不同的顺式活性转录控制机制的差异活性介导的。确定这些顺式机制与选择之间的“转换”关系非常重要。

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