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MSX1/2 调节 MDM2 E3 连接酶依赖性血管钙化。

Regulation of MDM2 E3 ligase-dependent vascular calcification by MSX1/2.

机构信息

Department of Pharmacology, Chonnam National University Medical School, Hwasun, Jeollanamdo, 58128, Republic of Korea.

Basic Research Laboratory for Vascular Remodeling, Chonnam National University Medical School, Hwasun, Jeollanamdo, 58128, Republic of Korea.

出版信息

Exp Mol Med. 2021 Nov;53(11):1781-1791. doi: 10.1038/s12276-021-00708-6. Epub 2021 Nov 29.

Abstract

Vascular calcification increases morbidity and mortality in patients with cardiovascular and renal diseases. Previously, we reported that histone deacetylase 1 prevents vascular calcification, whereas its E3 ligase, mouse double minute 2 homolog (MDM2), induces vascular calcification. In the present study, we identified the upstream regulator of MDM2. By utilizing cellular models and transgenic mice, we confirmed that E3 ligase activity is required for vascular calcification. By promoter analysis, we found that both msh homeobox 1 (Msx1) and msh homeobox 2 (Msx2) bound to the MDM2 promoter region, which resulted in transcriptional activation of MDM2. The expression levels of both Msx1 and Msx2 were increased in mouse models of vascular calcification and in calcified human coronary arteries. Msx1 and Msx2 potentiated vascular calcification in cellular and mouse models in an MDM2-dependent manner. Our results establish a novel role for MSX1/MSX2 in the transcriptional activation of MDM2 and the resultant increase in MDM2 E3 ligase activity during vascular calcification.

摘要

血管钙化增加心血管和肾脏疾病患者的发病率和死亡率。此前,我们报道组蛋白去乙酰化酶 1 可预防血管钙化,而其 E3 连接酶,鼠双微体 2 同源物(MDM2)则诱导血管钙化。在本研究中,我们确定了 MDM2 的上游调节因子。通过利用细胞模型和转基因小鼠,我们证实 E3 连接酶活性是血管钙化所必需的。通过启动子分析,我们发现同源盒蛋白 1(Msx1)和同源盒蛋白 2(Msx2)都与 MDM2 启动子区域结合,导致 MDM2 的转录激活。在血管钙化的小鼠模型和钙化的人类冠状动脉中,Msx1 和 Msx2 的表达水平均增加。Msx1 和 Msx2 以 MDM2 依赖的方式增强细胞和小鼠模型中的血管钙化。我们的研究结果确立了 MSX1/MSX2 在 MDM2 的转录激活以及血管钙化过程中 MDM2 E3 连接酶活性增加中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3772/8639964/663a3a1f035d/12276_2021_708_Fig1_HTML.jpg

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