| Autor: |
Joll JE 2nd; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee., Riley LA; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee., Bersi MR; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee., Nyman JS; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee.; Department of Orthopedic Surgery, Vanderbilt University Medical Center, Nashville, Tennessee.; Center for Bone Biology, Vanderbilt University Medical Center, Nashville, Tennessee.; Department of Veterans Affairs, Tennessee Valley Healthcare System, Nashville, Tennessee., Merryman WD; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee. |
| Jazyk: |
angličtina |
| Zdroj: |
American journal of physiology. Heart and circulatory physiology [Am J Physiol Heart Circ Physiol] 2022 Nov 01; Vol. 323 (5), pp. H1037-H1047. Date of Electronic Publication: 2022 Oct 14. |
| DOI: |
10.1152/ajpheart.00355.2022 |
| Abstrakt: |
The objective of this study was to test the hypothesis that targeting sclerostin would accelerate the progression of aortic valve stenosis. Sclerostin (mouse gene, Sost ) is a secreted glycoprotein that acts as a potent regulator of bone remodeling. Antibody therapy targeting sclerostin is approved for osteoporosis but results from a stage III clinical trial showed multiple off-target cardiovascular effects. Wild-type (WT, Sost +/+ ) and Sost -gene knockout-expression (Null, Sost -/- ) mice were generated and maintained to 12 mo of age on a high-cholesterol diet to induce aortic valve stenosis. Mice were examined by echocardiography, histology, and RNAseq. Immortalized valve interstitial cells were developed from each genotype for in vitro studies. Null mice developed a bone overgrowth phenotype, similar to patients with sclerosteosis. Surprisingly, however, WT mice developed hemodynamic signs of aortic valve stenosis, whereas Null mice were unchanged. WT mice had thicker aortic valve leaflets and higher amounts of α-smooth muscle actin, a marker myofibroblast activation and dystrophic calcification, with very little evidence of Runx2 expression, a marker of osteogenic calcification. RNAseq analysis of aortic roots indicated the HOX family of transcription factors was significantly upregulated in Null mice, and valve interstitial cells from Null animals were enriched with Hoxa1, Hoxb2, and Hoxd3 subtypes with downregulated Hoxa7. In addition, Null valve interstitial cells were shown to be less contractile than their WT counterparts. Contrary to our hypothesis, sclerostin targeting prevented hallmarks of aortic valve stenosis and indicates that targeted antibody treatments for osteoporosis may be beneficial for these patients regarding aortic stenosis. NEW & NOTEWORTHY We have found that genetic ablation of the Sost gene (protein: sclerostin) prevents aortic valve stenosis in aged, Western diet mice. This is a new role for sclerostin in the cardiovascular system. To the knowledge of the authors, this is one of the first studies directly manipulating sclerostin in a cardiovascular disease model and the first to specifically study the aortic valve. We also provide a potential new role for Hox genes in cardiovascular disease, noting pan- Hox upregulation in the aortic roots of sclerostin genetic knockouts. The role of Hox genes in postnatal cardiovascular health and disease is another burgeoning field of study to which this article contributes. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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