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AR 促进 YAP-TEAD 与 AM 启动子相互作用,增强肥大细胞浸润到皮肤神经纤维瘤中。

AR facilitates YAP-TEAD interaction with the AM promoter to enhance mast cell infiltration into cutaneous neurofibroma.

机构信息

Department of Plastic, Cosmetic and Maxillofacial Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.

The School of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

出版信息

Sci Rep. 2019 Dec 18;9(1):19346. doi: 10.1038/s41598-019-56022-9.

Abstract

Abundant mast cell infiltration and disease initiation at puberty are hallmark features of cutaneous neurofibroma (cNF). However, the association between mast cell infiltration and steroid hormones in cNF remains unclear. Here, we determined that androgen receptor (AR) expression is positively associated with mast cell density in cNF tissues. Moreover, both in vitro cell experiments and in vivo mouse models verified that activated AR promoted mast cell infiltration and that AR inhibition reduced mast cell infiltration. Analyses in cell models and xenograft tumours both demonstrated that AR upregulated Yes associate  protein 1 (YAP)-adrenomedullin (AM) signalling. Clinical samples from cNF patients further verified that AR was positively related to YAP and AM. Mechanistic analysis revealed that AR accelerates AM transcription via enhancing YAP- TEA domain transcription factor (TEAD) binding to the AM promoter. Consequently, the upregulated AM enhanced mast cell recruitment. Interruption of the YAP-TEAD interaction or inhibition of AM could impair mast cell accumulation induced by active AR, which indicated that this newly found signalling pathway may provide novel targets for cNF treatment.

摘要

大量肥大细胞浸润和青春期发病是皮肤神经纤维瘤 (cNF) 的标志性特征。然而,cNF 中肥大细胞浸润与类固醇激素之间的关联尚不清楚。在这里,我们确定雄激素受体 (AR) 的表达与 cNF 组织中的肥大细胞密度呈正相关。此外,体外细胞实验和体内小鼠模型都验证了激活的 AR 促进了肥大细胞浸润,而 AR 抑制减少了肥大细胞浸润。在细胞模型和异种移植瘤中的分析均表明,AR 上调了 Yes 相关蛋白 1 (YAP)-肾上腺髓质素 (AM) 信号。来自 cNF 患者的临床样本进一步证实,AR 与 YAP 和 AM 呈正相关。机制分析表明,AR 通过增强 YAP-TEAD 转录因子 (TEAD) 与 AM 启动子的结合来加速 AM 的转录。因此,上调的 AM 增强了肥大细胞的募集。YAP-TEAD 相互作用的中断或 AM 的抑制可损害由活性 AR 诱导的肥大细胞积累,这表明这条新发现的信号通路可能为 cNF 的治疗提供新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d57c/6920444/e2e01990e844/41598_2019_56022_Fig1_HTML.jpg

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