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Skeletal muscle-specific forkhead box protein-O1 overexpression suppresses atherosclerosis progression in apolipoprotein E-knockout mice.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2021 Feb 12; Vol. 540, pp. 61-66. Date of Electronic Publication: 2021 Jan 12. - Publication Year :
- 2021
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Abstract
- Calorie restriction (CR) reportedly prevents atherosclerotic diseases. Furthermore, CR induces forkhead box protein-O1 (FOXO-1) expression in the skeletal muscle, altering the character of the skeletal muscle. We previously reported that the change in skeletal muscle character, induced by the overexpression of peroxisome proliferator-activated receptor γ coactivator-1α, suppresses atherosclerotic progression in an atherosclerotic apolipoprotein E-knockout (ApoE-KO) mouse model. Thus, we hypothesized that skeletal muscle alternation induced by FOXO-1 may also have an anti-atherosclerotic effect in ApoE-KO mice. In this study, we investigated whether skeletal muscle-specific FOXO-1 overexpression suppresses the progression of atherosclerosis in ApoE-KO mice. We generated ApoE-KO/FOXO-1 mice, in which an ApoE-KO mouse was crossbred with a mouse presenting skeletal muscle-specific FOXO-1 overexpression (FOXO-1Tg). The mice were sacrificed at 20 weeks of age, and atherosclerotic plaque area and protein expression in the plaque were measured. Additionally, we measured the tumor necrosis factor α (TNFα)- induced mRNA expression in human umbilical vein endothelial cells (HUVECs), using serum collected from the FOXO-1Tg mice. Accordingly, ApoE-KO/FOXO-1 mice showed a 65% reduced atherosclerotic plaque area when compared with the ApoE-KO mice, with concomitantly reduced vascular cell adhesion molecule-1 (VCAM-1) and macrophage infiltration. As compared to serum from wild-type mice, the serum collected from the FOXO-1Tg mice significantly suppressed the mRNA expression of VCAM-1, an atherosclerosis initiation factor, in TNFα-treated HUVECs. Therefore, these data suggest that skeletal muscle-specific FOXO-1 overexpression suppresses the progression of atherosclerosis in ApoE-KO mice. In part, the CR-induced anti-atherosclerotic effect could be attributed to FOXO-1 upregulation in the skeletal muscle.<br />Competing Interests: Declaration of competing interest We have no conflict of interest to disclose.<br /> (Copyright © 2021 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Apolipoproteins E genetics
Human Umbilical Vein Endothelial Cells
Humans
Macrophages metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Tumor Necrosis Factor-alpha metabolism
Vascular Cell Adhesion Molecule-1 metabolism
Apolipoproteins E deficiency
Atherosclerosis genetics
Atherosclerosis pathology
Disease Progression
Forkhead Box Protein O1 genetics
Forkhead Box Protein O1 metabolism
Muscle, Skeletal metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 540
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 33450481
- Full Text :
- https://doi.org/10.1016/j.bbrc.2021.01.001