[FoxN1、p63 和 AIRE 对年龄相关胸腺内陷过程的影响:最新进展]。

Jiayi Wang, Jun Li, Xinsheng Yao
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引用次数: 0

摘要

随着年龄的增长,与年龄相关的胸腺内陷会导致退行性疾病、自身免疫性疾病、肿瘤和机会性感染。叉头盒 N1(FoxN1)、p63 和自身免疫调节剂(AIRE)等转录因子可通过调节胸腺上皮细胞(TECs)的增殖、发育和分化,影响与年龄相关的胸腺内陷过程以及 T 细胞的分化、发育和输出。在此,我们回顾了与年龄相关的胸腺萎缩的调控机制,以及对FoxN1、p63和AIRE的上下游靶点、影响其功能的miRNA和信号通路的新治疗方案的研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of FoxN1, p63 and AIRE on the process of age-related thymus involution: An update].

Age-related thymus involution that comes with age, can lead to degenerative diseases, autoimmune diseases, tumors and opportunistic infections. Transcription factors such as forkhead box N1 (FoxN1), p63 and autoimmune regulator (AIRE) that can affect the process of age-related thymus involution and the differentiation, development and output of T cells by regulating the proliferation, development and differentiation of thymic epithelial cells(TECs). Here, we reviewed the mechanism of regulating age-related thymus involution and the research into the new treatment schemes progresses in the upstream and downstream targets of FoxN1, p63 and AIRE, miRNAs and signal pathways that affect their functions.

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