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本文引用的文献

1
miR-203 represses 'stemness' by repressing DeltaNp63.微小RNA-203通过抑制DeltaNp63来抑制“干性”。
Cell Death Differ. 2008 Jul;15(7):1187-95. doi: 10.1038/cdd.2008.69. Epub 2008 May 16.
2
Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input.表达艾里蛋白的髓质胸腺上皮细胞发育过程中的连续阶段涉及不同的细胞输入。
Eur J Immunol. 2008 Apr;38(4):942-7. doi: 10.1002/eji.200738052.
3
A specific anti-Aire antibody reveals aire expression is restricted to medullary thymic epithelial cells and not expressed in periphery.一种特异性抗艾里蛋白抗体显示,艾里蛋白的表达仅限于胸腺髓质上皮细胞,在外周不表达。
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A skin microRNA promotes differentiation by repressing 'stemness'.一种皮肤微小RNA通过抑制“干性”来促进分化。
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Transcriptional control of the differentiation program of interfollicular epidermal keratinocytes.毛囊间表皮角质形成细胞分化程序的转录调控
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Generating intrathymic microenvironments to establish T-cell tolerance.生成胸腺内微环境以建立T细胞耐受性。
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FGFR2IIIb signaling regulates thymic epithelial differentiation.FGFR2IIIb信号传导调节胸腺上皮分化。
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AIRE recruits P-TEFb for transcriptional elongation of target genes in medullary thymic epithelial cells.AIRE招募P-TEFb以促进髓质胸腺上皮细胞中靶基因的转录延伸。
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Proliferative arrest and rapid turnover of thymic epithelial cells expressing Aire.表达艾里蛋白的胸腺上皮细胞的增殖停滞和快速更新。
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自身免疫调节因子缺陷型胸腺中髓质上皮区室的改变:对胸腺上皮细胞分化程序的影响

Alterations of the medullary epithelial compartment in the Aire-deficient thymus: implications for programs of thymic epithelial differentiation.

作者信息

Dooley James, Erickson Matthew, Farr Andrew G

机构信息

Department of Biological Structure, University of Washington, Seattle, WA 98195, USA.

出版信息

J Immunol. 2008 Oct 15;181(8):5225-32. doi: 10.4049/jimmunol.181.8.5225.

DOI:10.4049/jimmunol.181.8.5225
PMID:18832676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2677919/
Abstract

A widely held model of thymic epithelial differentiation is based on patterns of keratin expression, where a K8(+)K5(+) progenitor gives rise to K8(+)K5/K14(-) cortical thymic epithelium (CTEC), and medullary thymic epithelium (MTEC) are K8(-)K5(+)K14(+). The thymic phenotype of p63-deficient mice indicates that p63 is an important regulator of proximal stages of thymic epithelial differentiation. In this study, we have examined several features of the thymic medullary compartment in wild-type and Aire-deficient thymi in an effort to integrate the proapoptotic activity of Aire with these different perspectives of TE differentiation. Patterns of keratin and p63 expression by MTEC described here are difficult to reconcile with postmitotic MTEC that express a K8(-)K14(+) phenotype and suggest that the patterns of p63 and keratin expression reflecting differentiation programs of other epithelial tissues provide a useful framework for revising models of TE differentiation. Alterations of the Aire(-/-) MTEC compartment included reduced expression of p63, increased frequency of MTEC expressing truncated Aire protein, and shifts in the pattern of keratin expression and epithelial morphology. These data suggest a scenario where cellular targets of Aire-mediated apoptosis are postmitotic MTEC that have not yet completed their terminal differentiation program. According to this view, the minor population of globular K8(+)K14(-/low) MTEC observed in the Aire(+/+) thymus and significantly expanded in the Aire(-/-) thymic medulla represent end-stage, terminally differentiated MTEC. These Aire-dependent alterations of the MTEC compartment suggest that the activity of Aire is not neutral with respect to the program of MTEC differentiation.

摘要

一种广泛认可的胸腺上皮分化模型是基于角蛋白表达模式,其中K8(+)K5(+)祖细胞产生K8(+)K5/K14(-)皮质胸腺上皮(CTEC),而髓质胸腺上皮(MTEC)为K8(-)K5(+)K14(+)。p63缺陷小鼠的胸腺表型表明p63是胸腺上皮分化近端阶段的重要调节因子。在本研究中,我们检查了野生型和Aire缺陷型胸腺中胸腺髓质区室的几个特征,以便将Aire的促凋亡活性与TE分化的这些不同观点整合起来。此处描述的MTEC的角蛋白和p63表达模式难以与表达K8(-)K14(+)表型的有丝分裂后MTEC相协调,这表明反映其他上皮组织分化程序的p63和角蛋白表达模式为修订TE分化模型提供了一个有用的框架。Aire(-/-) MTEC区室的改变包括p63表达降低、表达截短Aire蛋白的MTEC频率增加,以及角蛋白表达模式和上皮形态的改变。这些数据表明一种情况,即Aire介导的凋亡的细胞靶点是尚未完成其终末分化程序的有丝分裂后MTEC。根据这一观点,在Aire(+/+)胸腺中观察到并在Aire(-/-)胸腺髓质中显著扩增的少量球状K8(+)K14(-/低) MTEC代表终末阶段、终末分化的MTEC。MTEC区室的这些Aire依赖性改变表明,Aire的活性对于MTEC分化程序并非是中性的。