Saturated fatty acid promotes calcification via suppressing SIRT6 expression in vascular smooth muscle cells

Author:

Tao Yafen12,Wu Yue12,Jiang Chuanyue12,Wang Qianghua3,Geng Xu4,Chen Lei1,Zhou Sihui1,Wang Xuegu2,Han Mingliang1,Du Danli2,Ding Biao2,Li Xiang1

Affiliation:

1. Anhui Province Key Laboratory of Clinical and Preclinical Research in Respiratory Disease, Molecular Diagnosis Center

2. Reproductive Medicine Center

3. Anhui Province Key Laboratory of Immunology in Chronic Diseases

4. Department of Cardiovascular Disease, First Affiliated Hospital of Bengbu Medical College, Bengbu, China

Abstract

Background: This study aims to investigate the effects of saturated free fatty acid on calcification and SIRT6 expression in vascular smooth muscle cells (VSMCs) and the role of SIRT6 in regulating VSMC calcification. Methods: Sprague–Dawley rats were randomly allocated to two groups: rats with normal diet (ND) and high-fat diet (HFD) from 4 to 12 weeks. At 12 weeks, part rats randomly selected from ND and HFD were administrated with vitamin D3 and nicotine to establish a model of vascular calcification. Thoracic aortas were collected from treatment rats at 16 weeks for assaying vascular calcification and related protein expression. Primary VSMCs isolated from Sprague–Dawley rats were used for investigating the effects of palmitic acid on VSMCs’ calcification, apoptosis and target protein expression. Results: HFD-facilitated calcification in medial aorta, with decreased SIRT6 expression in VSMCs of aortas. Palmitic acid decreased SIRT6 expression while increased calcification, apoptosis and protein expression of BMP2 and RUNX2 in primary VSMCs. Overexpression of SIRT6 could, partially or completely, rescue the palmitic acid-induced elevation of calcification, apoptosis and expression of BMP2 and RUNX2. Conclusion: This study demonstrated that vascular calcification induced by HFD was linked to the palmitic acid-induced downregulation of SIRT6. Overexpression of SIRT6 could decrease palmitic acid-induced calcification and apoptosis in VSMCs.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology,Internal Medicine

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