Dooley James, Erickson Matthew, Farr Andrew G
Department of Biological Structure, University of Washington, Seattle, WA 98195, USA.
J Immunol. 2008 Oct 15;181(8):5225-32. doi: 10.4049/jimmunol.181.8.5225.
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.
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。