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炎症因子和机械应激对人肺内皮细胞中皮层肌动蛋白(CTTN)的遗传和表观遗传调控

Genetic and epigenetic regulation of cortactin (CTTN) by inflammatory factors and mechanical stress in human lung endothelial cells.

作者信息

Sun Xiaoguang, Sun Belinda, Sammani Saad, Dudek Steven M, Belvitch Patrick, Camp Sara M, Zhang Donna, Bime Christian, Garcia Joe G N

机构信息

Department of Medicine, University of Arizona, Tucson, AZ, U.S.A.

Department of Pathology, University of Arizona, Tucson, AZ, U.S.A.

出版信息

Biosci Rep. 2024 Sep 25;44(9). doi: 10.1042/BSR20231934.

Abstract

RATIONALE

Cortactin, an actin-binding cytoskeletal protein, plays a crucial role in maintaining endothelial cell (EC) barrier integrity and regulating vascular permeability. The gene encoding cortactin, CTTN, is implicated in various lung inflammatory disorders. Despite this, the transcriptional regulation of CTTN by inflammatory stimuli and promoter SNPs remains unexplored.

METHODS

We transfected human lung ECs with a full-length CTTN promoters linked to a luciferase reporter to measure promoter activity. SNP-containing CTTN promoter was created via site-directed mutagenesis. Transfected ECs were exposed to LPS (PAMP), TNF-α (cytokine), cyclic stretch (CS), FG-4592 (HIF-inducer), NRF2 (anti-oxidant modulator), FTY-(S)-phosphate (endothelial barrier enhancer), and 5'-Aza (demethylation inducer). Immunohistochemistry was used to assess cortactin expression in mouse lungs exposed to LPS.

RESULTS

LPS, TNF-α, and 18%CS significantly increased CTTN promoter activities in a time-dependent manner (P<0.05). The variant rs34612166 (-212T/C) markedly enhanced LPS- and 18%CS- induced CTTN promoter activities (P<0.05). FG-4592 significantly boosted CTTN promoter activities (P<0.01), which were partially inhibited by HIF1α (KC7F2) and HIF2α (PT2385) inhibitors (P<0.05). NRF2 activator Bixin increased CTTN promoter activities, whereas NRF2 inhibitor Brusatol reduced them (P<0.05). 5'-Aza increased CTTN promoter activities by 2.9-fold (P<0.05). NF-κB response element mutations significantly reduced CTTN promoter activities response to LPS and TNFα. FTY-(S)-phosphate significantly increased CTTN promoter activities in 24 h. In vivo, cortactin levels were significantly elevated in inflammatory mouse lungs exposed to LPS for 18 h.

CONCLUSION

CTTN transcriptional is significantly influenced by inflammatory factors and promoter variants. Cortactin, essential in mitigating inflammatory edema, presents a promising therapeutic target to alleviate severe inflammatory disorders.

摘要

原理

皮层肌动蛋白是一种与肌动蛋白结合的细胞骨架蛋白,在维持内皮细胞(EC)屏障完整性和调节血管通透性方面发挥着关键作用。编码皮层肌动蛋白的基因CTTN与多种肺部炎症性疾病有关。尽管如此,炎症刺激和启动子单核苷酸多态性对CTTN的转录调控仍未得到探索。

方法

我们用与荧光素酶报告基因相连的全长CTTN启动子转染人肺内皮细胞,以测量启动子活性。通过定点诱变创建含单核苷酸多态性的CTTN启动子。将转染后的内皮细胞暴露于脂多糖(PAMP)、肿瘤坏死因子-α(细胞因子)、周期性拉伸(CS)、FG-4592(低氧诱导因子诱导剂)、核因子E2相关因子2(NRF2,抗氧化调节剂)、FTY-(S)-磷酸盐(内皮屏障增强剂)和5'-氮杂胞苷(去甲基化诱导剂)。采用免疫组织化学法评估暴露于脂多糖的小鼠肺组织中皮层肌动蛋白的表达。

结果

脂多糖、肿瘤坏死因子-α和18%的周期性拉伸以时间依赖性方式显著增加CTTN启动子活性(P<0.05)。变异体rs34612166(-212T/C)显著增强脂多糖和18%周期性拉伸诱导的CTTN启动子活性(P<0.05)。FG-4592显著提高CTTN启动子活性(P<0.01),其活性被低氧诱导因子-1α(KC7F2)和低氧诱导因子-2α(PT2385)抑制剂部分抑制(P<0.05)。核因子E2相关因子2激活剂β-胡萝卜素增加CTTN启动子活性,而核因子E2相关因子2抑制剂布鲁斯他汀则降低其活性(P<0.05)。5'-氮杂胞苷使CTTN启动子活性增加2.9倍(P<0.05)。核因子-κB反应元件突变显著降低CTTN启动子对脂多糖和肿瘤坏死因子-α的反应活性。FTY-(S)-磷酸盐在24小时内显著增加CTTN启动子活性。在体内,暴露于脂多糖18小时的炎症小鼠肺组织中皮层肌动蛋白水平显著升高。

结论

CTTN转录受炎症因子和启动子变异的显著影响。皮层肌动蛋白在减轻炎症性水肿中起重要作用,是缓解严重炎症性疾病的一个有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c38/11405783/cf299a231a7d/bsr-44-bsr20231934-g1.jpg

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