胸腺的三维结构对于维持诱导T细胞发育所必需的δ样蛋白表达是必要的。

Three-dimensional architecture of the thymus is required to maintain delta-like expression necessary for inducing T cell development.

作者信息

Mohtashami Mahmood, Zúñiga-Pflücker Juan Carlos

机构信息

Department of Immunology, University of Toronto, and Sunnybrook & Women's Research Institute, Toronto, Ontario, Canada.

出版信息

J Immunol. 2006 Jan 15;176(2):730-4. doi: 10.4049/jimmunol.176.2.730.

Abstract

The three-dimensional microarchitecture of the thymus plays a unique role in directing T cell lineage commitment and development. This is supported by the fact that, in contrast to fetal thymic organ cultures, thymic stromal cell monolayer cultures (TSMC) fail to support T lymphopoiesis. Nevertheless, OP9-DL1 cell monolayer cultures induce T lineage commitment and differentiation. Thus, the inability of TSMC to support T lymphopoiesis may be due to a loss of Notch ligand expression and/or function during culture. In this study, we report that, in contrast to fetal thymic organ cultures, TSMC fail to maintain expression of the Notch ligands, Delta-like (Dll) 1 and Dll4, and concomitantly lose the ability to support T lymphopoiesis. Importantly, ectopic re-expression of Dll1 or Dll4 is sufficient to restore the ability of TSMC to support T lymphopoiesis. These findings demonstrate that maintenance of endogenous Dll1 or Dll4 expression by thymic stromal cells is required for the commitment and differentiation of T cells in the absence of a three-dimensional microenvironment.

摘要

胸腺的三维微结构在指导T细胞谱系定向和发育过程中发挥着独特作用。这一点得到了以下事实的支持:与胎儿胸腺器官培养不同,胸腺基质细胞单层培养(TSMC)无法支持T淋巴细胞生成。然而,OP9-DL1细胞单层培养可诱导T谱系定向和分化。因此,TSMC无法支持T淋巴细胞生成可能是由于培养过程中Notch配体表达和/或功能丧失所致。在本研究中,我们报告称,与胎儿胸腺器官培养不同,TSMC无法维持Notch配体Delta样(Dll)1和Dll4的表达,并随之失去支持T淋巴细胞生成的能力。重要的是,异位重新表达Dll1或Dll4足以恢复TSMC支持T淋巴细胞生成的能力。这些发现表明,在缺乏三维微环境的情况下,胸腺基质细胞维持内源性Dll1或Dll4表达是T细胞定向和分化所必需的。

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