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靶向sortilin的反义寡核苷酸以性别依赖方式减少小鼠血管钙化。

Antisense Oligonucleotide Targeting Sortilin Reduces Vascular Calcification in Mice in a Sex-Dependent Manner.

作者信息

Lupieri Adrien, Becker-Greene Dakota, Le Thanh-Dat, Roschel Marina M, Jha Prabhash K, Sonawane Abhijeet R, Mullick Adam, Tsimikas Sotirios, Kuraoka Shiori, Singh Sasha A, Aikawa Masanori, Aikawa Elena

机构信息

Division of Cardiovascular Medicine, Center for Excellence in Vascular Biology (A.L., D.B.-G., T.-D.L., M.M.R., P.K.J., A.R.S., M.A., E.A.), Brigham and Women's Hospital, Harvard Medical School, Boston, MA.

Faculty of Medicine, University of São Paulo, Brazil (M.M.R.).

出版信息

Arterioscler Thromb Vasc Biol. 2025 Aug;45(8):1398-1415. doi: 10.1161/ATVBAHA.124.321999. Epub 2025 Jun 12.

Abstract

BACKGROUND

Atherosclerotic calcification is a complex pathological process associated with an increased risk of cardiovascular events. Despite extensive research, this disorder has no effective therapeutic strategies. In this study, we evaluated the therapeutic potential of silencing Sort (sortilin) expression in vivo using antisense oligonucleotide (ASO-Sort1) to reduce the development of atherosclerosis and associated calcification.

METHODS

Male and female (low-density lipoprotein receptor knock-out) mice were fed a high-fat diet and treated with ASO-Sort1 for 15 weeks. After ASO-Sort1 treatment, we evaluated atherosclerotic lesion formation and calcification through molecular imaging and histological techniques. The levels of plasma lipid and inflammatory molecules were determined. Unbiased liquid chromatography-mass spectrometry-based proteomics of aortic arches was conducted to investigate the sex-specific regulation in ASO-Sort1-treated mice. To validate our in vivo findings, we conducted in vitro experiments to examine whether β-estradiol treatment of mouse smooth muscle cells promotes calcification independently of Sort.

RESULTS

ASO targeted primarily arterial smooth muscle cells, leading to a comparable reduction of aortic Sort1 expression by ≈57% in males and 52% in females. Although ASO-Sort1 did not affect the size of atherosclerotic lesions, it significantly reduced necrotic core development by 60% in male and 40% in female mice. In addition, it prevented aortic calcification by >50% only in male mice. Furthermore, proteome analysis revealed that while this treatment reduced vesicular trafficking, immune system, and extracellular matrix organization pathways in both male and female mice, it reduced autophagy-related processes specifically in males. In vitro results indicated that β-estradiol promotes calcification in smooth muscle cells treated with ASO-Sort1 by altering autophagy.

CONCLUSIONS

Targeting Sort using antisense technology is effective in preventing vascular calcification in male mice. This unexpected outcome highlighted a novel sex-dependent discrepancy of the calcification pathway implicating the alteration of autophagy by β-estradiol and Sort.

摘要

背景

动脉粥样硬化钙化是一个复杂的病理过程,与心血管事件风险增加相关。尽管进行了广泛研究,但这种疾病尚无有效的治疗策略。在本研究中,我们评估了使用反义寡核苷酸(ASO-Sort1)在体内沉默Sort(sortilin)表达以减少动脉粥样硬化及其相关钙化发展的治疗潜力。

方法

给雄性和雌性(低密度脂蛋白受体敲除)小鼠喂食高脂饮食,并使用ASO-Sort1治疗15周。在ASO-Sort1治疗后,我们通过分子成像和组织学技术评估动脉粥样硬化病变形成和钙化情况。测定血浆脂质和炎症分子水平。对主动脉弓进行基于无偏液相色谱-质谱的蛋白质组学分析,以研究ASO-Sort1治疗小鼠中的性别特异性调控。为了验证我们的体内研究结果,我们进行了体外实验,以检查β-雌二醇处理小鼠平滑肌细胞是否独立于Sort促进钙化。

结果

ASO主要靶向动脉平滑肌细胞,导致雄性小鼠主动脉Sort1表达降低约57%,雌性小鼠降低52%。虽然ASO-Sort1不影响动脉粥样硬化病变大小,但它显著减少了雄性小鼠坏死核心的发展,减少了60%,雌性小鼠减少了40%。此外,它仅在雄性小鼠中使主动脉钙化减少>50%。此外,蛋白质组分析表明,虽然这种治疗减少了雄性和雌性小鼠的囊泡运输、免疫系统和细胞外基质组织途径,但它专门减少了雄性小鼠中与自噬相关的过程。体外结果表明,β-雌二醇通过改变自噬促进ASO-Sort1处理的平滑肌细胞钙化。

结论

使用反义技术靶向Sort可有效预防雄性小鼠的血管钙化。这一意外结果突出了钙化途径中一种新的性别依赖性差异,涉及β-雌二醇和Sort对自噬的改变。

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