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Wnt4信号通路与年龄相关的胸腺退化过程中增殖减少和细胞凋亡增加有关。

Wnt4 signaling is associated with the decrease of proliferation and increase of apoptosis during age-related thymic involution.

作者信息

Wei Tianli, Zhang Nannan, Guo Zhibin, Chi Feng, Song Yan, Zhu Xike

机构信息

Research Center, Shengjing Hospital, China Medical University, Shenyang, Liaonining 110004, P.R. China.

出版信息

Mol Med Rep. 2015 Nov;12(5):7568-76. doi: 10.3892/mmr.2015.4343. Epub 2015 Sep 21.

Abstract

The thymus is a central lymphoid organ that is responsible for T-lymphocyte development and maturation. Through negative and positive selection, lymphoid progenitor cells, which initiate from the bone marrow, develop into mature T cells in the thymus, and are subsequently involved in peripheral cell immunity. It has been reported that the Wnt signaling pathway exists widely in thymic epithelial cells and T lymphocytes. Wnt signaling affects the shape and function of thymic epithelial cells and has an important role in maintaining pro‑T‑cells, and in the subsequent T‑cell differentiation. Previous studies have demonstrated that the Wnt signaling pathway participates in age‑associated thymic involution. In the present study alterations in proliferation and apoptosis were investigated in murine thymic cells during aging. The results of the present study demonstrated that the aged thymus was characterized by markedly decreased cell numbers, as well as decreased proliferation and increased apoptosis. Concurrently, age‑associated changes in thymic cell number and function were accompanied by a decrease in the transcription levels of Wnt4, and downregulation of forkhead box N1 and B‑cell lymphoma‑extra large, which are two target genes of the Wnt4 signaling pathway. In vitro studies demonstrated that activation of the Wnt4 signaling pathway promotes mouse thymus epithelial cell 1 (MTEC1) cell proliferation, and that Wnt4 signaling modulation alleviates dexamethasone‑mediated MTEC1 cell apoptosis. These results suggest that normal expression levels of Wnt4 have a critical role in maintaining the balance between cell proliferation and apoptosis. Alterations in the Wnt signaling pathway may disrupt the epithelial network structure of the thymus, eventually leading to microenvironmental damage. Therefore, further studies regarding the effects of the Wnt signaling pathway on thymus development and age-related thymic involution, may be beneficial for improving the health conditions of the elderly.

摘要

胸腺是一个中枢淋巴器官,负责T淋巴细胞的发育和成熟。通过阴性和阳性选择,起源于骨髓的淋巴祖细胞在胸腺中发育为成熟的T细胞,随后参与外周细胞免疫。据报道,Wnt信号通路广泛存在于胸腺上皮细胞和T淋巴细胞中。Wnt信号影响胸腺上皮细胞的形态和功能,在维持前T细胞以及随后的T细胞分化中发挥重要作用。先前的研究表明,Wnt信号通路参与与年龄相关的胸腺退化。在本研究中,对衰老过程中小鼠胸腺细胞的增殖和凋亡变化进行了研究。本研究结果表明,衰老的胸腺其特征是细胞数量显著减少,增殖降低且凋亡增加。同时,胸腺细胞数量和功能的年龄相关变化伴随着Wnt4转录水平的降低,以及Wnt4信号通路的两个靶基因叉头框N1和B细胞淋巴瘤-特大基因的下调。体外研究表明,Wnt4信号通路的激活促进小鼠胸腺上皮细胞1(MTEC1)的增殖,并且Wnt4信号调节减轻地塞米松介导的MTEC1细胞凋亡。这些结果表明,Wnt4的正常表达水平在维持细胞增殖和凋亡之间的平衡中起关键作用。Wnt信号通路的改变可能破坏胸腺的上皮网络结构,最终导致微环境损伤。因此,进一步研究Wnt信号通路对胸腺发育和与年龄相关的胸腺退化的影响,可能有助于改善老年人的健康状况。

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