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RUNX 转录因子对于维持附睾上皮细胞的分化是必不可少的。

RUNX transcription factors are essential in maintaining epididymal epithelial differentiation.

机构信息

Institute of Biomedicine, Cancer Research Unit and FICAN West Cancer Centre Laboratory, University of Turku and Turku University Hospital, Turku, Finland.

Institute of Biomedicine, Research Centre for Integrative Physiology and Pharmacology, Turku Center for Disease Modeling, University of Turku, Turku, Finland.

出版信息

Cell Mol Life Sci. 2024 Apr 17;81(1):183. doi: 10.1007/s00018-024-05211-5.

Abstract

Apart from the androgen receptor, transcription factors (TFs) that are required for the development and formation of the different segments of the epididymis have remained unknown. We identified TF families expressed in the developing epididymides, of which many showed segment specificity. From these TFs, down-regulation of runt related transcription factors (RUNXs) 1 and 2 expression coincides with epithelial regression in Dicer1 cKO mice. Concomitant deletion of both Runx1 and Runx2 in a mouse epididymal epithelial cell line affected cell morphology, adhesion and mobility in vitro. Furthermore, lack of functional RUNXs severely disturbed the formation of 3D epididymal organoid-like structures. Transcriptomic analysis of the epididymal cell organoid-like structures indicated that RUNX1 and RUNX2 are involved in the regulation of MAPK signaling, NOTCH pathway activity, and EMT-related gene expression. This suggests that RUNXs are master regulators of several essential signaling pathways, and necessary for the maintenance of proper differentiation of the epididymal epithelium.

摘要

除了雄激素受体,对于精子在附睾不同部位发育和形成所必需的转录因子(TFs)仍不清楚。我们鉴定了在发育中的附睾中表达的 TF 家族,其中许多具有节段特异性。在这些 TFs 中,RUNX1 和 RUNX2 的下调与 Dicer1 cKO 小鼠中的上皮细胞退化同时发生。在小鼠附睾上皮细胞系中同时缺失 Runx1 和 Runx2 会影响细胞体外的形态、黏附和迁移。此外,功能性 RUNXs 的缺乏严重扰乱了 3D 附睾类器官样结构的形成。附睾细胞类器官样结构的转录组分析表明,RUNX1 和 RUNX2 参与了 MAPK 信号通路、NOTCH 途径活性和 EMT 相关基因表达的调节。这表明 RUNXs 是几个重要信号通路的主调控因子,对于维持附睾上皮细胞的正常分化是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4523/11072856/e7239a4d1b7d/18_2024_5211_Fig1_HTML.jpg

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