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在蜿蜒曲折中游走:关于成熟T细胞如何在胸腺中找到其曲折路径的分子见解。

Trafficking on serpentines: molecular insight on how maturating T cells find their winding paths in the thymus.

作者信息

Misslitz Ana, Bernhardt Günter, Förster Reinhold

机构信息

Institute of Immunology, Hannover Medical School, Hannover, Germany.

出版信息

Immunol Rev. 2006 Feb;209:115-28. doi: 10.1111/j.0105-2896.2006.00351.x.

Abstract

Maintenance of the peripheral T-cell pool throughout the life requires uninterrupted generation of T cells. The majority of peripheral T cells are generated in the thymus. However, the thymus does not contain hematopoietic progenitors with unlimited self-renewing potential, and continuous production of T cells requires importation of such progenitors from the bone marrow into the thymus. Thymus-homing progenitors enter the thymus and subsequently migrate throughout distinct intrathymic microenvironments while differentiating into mature T cells. At each step of this scheduled journey, developing thymocytes interact intimately with the local stroma, which allow them to proceed to the next stage of their differentiation and maturation program. Undoubtedly, thymocyte/stroma interactions are instrumental for both thymocytes and stroma, because only their ongoing interplay generates and maintains a fully operational thymus, able to guarantee unimpaired T-cell supply. Therefore, proper T-cell generation intrinsically involves polarized cell migration during both adult life and embryogenesis when the thymus primordium develops into a functional thymus. The molecular mechanisms controlling cell migration during thymus development and postnatal T-cell differentiation are beginning to be defined. This review focuses on recent data regarding the role of cell migration in both colonization of the fetal thymus and T-cell development during postnatal life in mice.

摘要

外周T细胞库在整个生命过程中的维持需要T细胞的不间断生成。大多数外周T细胞在胸腺中产生。然而,胸腺并不包含具有无限自我更新潜能的造血祖细胞,T细胞的持续产生需要将此类祖细胞从骨髓输入到胸腺中。归巢至胸腺的祖细胞进入胸腺,随后在不同的胸腺内微环境中迁移,同时分化为成熟T细胞。在这个预定旅程的每一步,发育中的胸腺细胞都与局部基质密切相互作用,这使它们能够进入分化和成熟程序的下一阶段。毫无疑问,胸腺细胞/基质相互作用对胸腺细胞和基质都至关重要,因为只有它们持续的相互作用才能产生并维持一个功能完全正常的胸腺,从而保证T细胞供应不受损害。因此,在成年期以及胚胎期(此时胸腺原基发育为功能性胸腺),适当的T细胞生成本质上都涉及极化细胞迁移。控制胸腺发育和出生后T细胞分化过程中细胞迁移的分子机制正开始得到阐明。本综述聚焦于关于细胞迁移在小鼠胎儿胸腺定植和出生后T细胞发育中作用的最新数据。

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