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二甲双胍介导的端粒稳定通过AMPK依赖的p-PGC-1α途径减轻动脉粥样硬化的进展。

Telomere stabilization by metformin mitigates the progression of atherosclerosis via the AMPK-dependent p-PGC-1α pathway.

作者信息

Sung Jin Young, Kim Seul Gi, Park So-Young, Kim Jae-Ryong, Choi Hyoung Chul

机构信息

Department of Pharmacology, College of Medicine, Yeungnam University, 170 Hyunchung-Ro, Nam-Gu, Daegu, 42415, Republic of Korea.

Senotherapy-based Metabolic Disease Control Research Center, College of Medicine, Yeungnam University, 170 Hyunchung-Ro, Nam-Gu, Daegu, 42415, Republic of Korea.

出版信息

Exp Mol Med. 2024 Sep;56(9):1967-1979. doi: 10.1038/s12276-024-01297-w. Epub 2024 Sep 2.

Abstract

Telomere dysfunction is a well-known molecular trigger of senescence and has been associated with various age-related diseases, including atherosclerosis. However, the mechanisms involved have not yet been elucidated, and the extent to which telomeres contribute to atherosclerosis is unknown. Therefore, we investigated the mechanism of metformin-induced telomere stabilization and the ability of metformin to inhibit vascular smooth muscle cell (VSMC) senescence caused by advanced atherosclerosis. The present study revealed that metformin inhibited the phenotypes of atherosclerosis and senescence in VSMCs. Metformin increased the phosphorylation of AMPK-dependent PGC-1α and thus increased telomerase activity and the protein level of TERT in OA-treated VSMCs. Mechanistically, the phosphorylation of AMPK and PGC-1α by metformin not only enhanced telomere function but also increased the protein level of TERT, whereas TERT knockdown accelerated the development of atherosclerosis and senescent phenotypes in OA-treated VSMCs regardless of metformin treatment. Furthermore, the in vivo results showed that metformin attenuated the formation of atherosclerotic plaque markers in the aortas of HFD-fed ApoE KO mice. Although metformin did not reduce plaque size, it inhibited the phosphorylation of the AMPK/PGC-1α/TERT signaling cascade, which is associated with the maintenance and progression of plaque formation, in HFD-fed ApoE KO mice. Accordingly, metformin inhibited atherosclerosis-associated phenotypes in vitro and in vivo. These observations show that the enhancement of telomere function by metformin is involved in specific signaling pathways during the progression of atherosclerosis. These findings suggest that telomere stabilization by metformin via the AMPK/p-PGC-1α pathway might provide a strategy for developing therapeutics against vascular diseases such as atherosclerosis.

摘要

端粒功能障碍是衰老的一个众所周知的分子触发因素,并且与包括动脉粥样硬化在内的各种年龄相关疾病有关。然而,其中涉及的机制尚未阐明,端粒对动脉粥样硬化的影响程度也未知。因此,我们研究了二甲双胍诱导端粒稳定的机制以及二甲双胍抑制晚期动脉粥样硬化引起的血管平滑肌细胞(VSMC)衰老的能力。本研究表明,二甲双胍抑制了VSMC中动脉粥样硬化和衰老的表型。二甲双胍增加了AMPK依赖性PGC-1α的磷酸化,从而增加了端粒酶活性以及OA处理的VSMC中TERT的蛋白水平。从机制上讲,二甲双胍对AMPK和PGC-1α的磷酸化不仅增强了端粒功能,还增加了TERT的蛋白水平,而TERT基因敲低加速了OA处理的VSMC中动脉粥样硬化和衰老表型的发展,无论是否进行二甲双胍治疗。此外,体内结果表明,二甲双胍减弱了高脂饮食喂养的ApoE基因敲除小鼠主动脉中动脉粥样硬化斑块标志物的形成。虽然二甲双胍没有减小斑块大小,但它抑制了高脂饮食喂养的ApoE基因敲除小鼠中与斑块形成的维持和进展相关的AMPK/PGC-1α/TERT信号级联的磷酸化。因此,二甲双胍在体外和体内均抑制了与动脉粥样硬化相关的表型。这些观察结果表明,二甲双胍对端粒功能的增强参与了动脉粥样硬化进展过程中的特定信号通路。这些发现表明,二甲双胍通过AMPK/p-PGC-1α途径实现的端粒稳定可能为开发针对动脉粥样硬化等血管疾病的治疗方法提供一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fd/11446938/8f0fc299b21d/12276_2024_1297_Fig1_HTML.jpg

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