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衰老小鼠胸腺的结构变化。

Architectural changes in the thymus of aging mice.

作者信息

Aw Danielle, Silva Alberto B, Maddick Mandy, von Zglinicki Thomas, Palmer Donald B

机构信息

Host Response and Genes and Development Group, Department of Veterinary Basic Sciences, Royal Veterinary College, Royal College Street, London NW1 0TU, UK.

出版信息

Aging Cell. 2008 Mar;7(2):158-67. doi: 10.1111/j.1474-9726.2007.00365.x. Epub 2008 Jan 28.

Abstract

Age-associated thymic involution is one of the most dramatic and ubiquitous changes in the immune system, although the precise mechanisms involved still remain obscured. Several hypotheses have been proposed incorporating extrinsic and intrinsic factors, however, changes in the thymic microenvironment itself is one of the least investigated. We therefore decided to undertake a detailed histological examination of the aging thymus in order to elucidate possible mechanisms of thymic atrophy. This investigation provides insight into the changes within the murine thymus with age, demonstrating a new approach to quantify protein expressional differences while preserving the thymic architecture. There is a decline in expression of thymic epithelial cell-specific makers and an increase in fibroblast content in the aging mouse thymus. This is concurrent with a disorganization of the thymic compartments, a morphological transformation within the epithelial cells and alterations of their archetypal staining patterns. Furthermore, this is linked to a rise in apoptotic cells and the novel finding of increased senescence in the thymus of older mice that appears to be colocalized in the epithelial compartment. These changes within the thymic epithelial cells may be in part accountable for thymic atrophy and responsible for the decline in T-cell output.

摘要

年龄相关的胸腺退化是免疫系统中最显著且普遍存在的变化之一,尽管其中涉及的精确机制仍不明晰。已经提出了几种包含外在和内在因素的假说,然而,胸腺微环境本身的变化是研究最少的因素之一。因此,我们决定对衰老的胸腺进行详细的组织学检查,以阐明胸腺萎缩的可能机制。这项研究深入了解了小鼠胸腺随年龄的变化,展示了一种在保留胸腺结构的同时量化蛋白质表达差异的新方法。在衰老的小鼠胸腺中,胸腺上皮细胞特异性标志物的表达下降,成纤维细胞含量增加。这与胸腺区室的紊乱、上皮细胞内的形态转变以及它们典型染色模式的改变同时发生。此外,这与凋亡细胞的增加以及老年小鼠胸腺中衰老增加这一新发现有关,衰老似乎在上皮区室中共定位。胸腺上皮细胞内的这些变化可能部分导致了胸腺萎缩,并导致T细胞输出下降。

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