共 22 条
Generation of both cortical and Aire+ medullary thymic epithelial compartments from CD205+ progenitors
被引:102
作者:
Baik, Song
[1
]
Jenkinson, Eric J.
[1
]
Lane, Peter J. L.
[1
]
Anderson, Graham
[1
]
Jenkinson, William E.
[1
]
机构:
[1] Univ Birmingham, Inst Biomed Res, MRC Ctr Immune Regulat, Birmingham B15 2TT, W Midlands, England
关键词:
Cellular immunology;
Developmental immunology;
Thymic epithelial cells;
STEM-CELLS;
MICROENVIRONMENT;
RECEPTOR;
LINEAGE;
MICE;
D O I:
10.1002/eji.201243209
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
In the adult thymus, the development of self-tolerant thymocytes requires interactions with thymic epithelial cells (TECs). Although both cortical and medullary TECs (cTECs/mTECs) are known to arise from common bipotent TEC progenitors, the phenotype of these progenitors and the timing of the emergence of these distinct lineages remain unclear. Here, we have investigated the phenotype and developmental properties of bipotent TEC progenitors during cTEC/mTEC lineage development. We show that TEC progenitors can undergo a stepwise acquisition of first cTEC and then mTEC hallmarks, resulting in the emergence of a progenitor population simultaneously expressing the cTEC marker CD205 and the mTEC regulator Receptor Activator of NF-B (RANK). In vivo analysis reveals the capacity of CD205+ TECs to generate functionally competent cortical and medullary microenvironments containing both cTECs and Aire+ mTECs. Thus, TEC development involves a stage in which bipotent progenitors can co-express hallmarks of the cTEC and mTEC lineages through sequential acquisition, arguing against a simple binary model in which both lineages diverge simultaneously from bipotent lineage negative TEC progenitors. Rather, our data reveal an unexpected overlap in the phenotypic properties of these bipotent TECs with their lineage-restricted counterparts.
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页码:589 / 594
页数:6
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