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Author Notes:

Ajit P. Yoganathan, ajit.yoganathan@bme.gatech.edu

Hanjoong Jo, hjo@emory.edu

MTS: executed the study, conducted all experiments, experimental and data analysis, and prepared the manuscript. NV-R: helped in experimental analysis and manuscript preparation. BV: helped in experimental analysis. HJ: co-principal investigator and provided supervision in all aspects of the study. AY: principal investigator and provided supervision in all aspects of the study. All authors contributed to the article and approved the submitted version.

We would like to thank Holifield Farms (Covington, GA) for graciously providing the porcine hearts.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Research Funding:

This work was supported by funding from the National Institutes of Health grants HL119798, HL139757, and HL151358 to HJ.

HJ was also supported by Wallace H. Coulter Distinguished Professor Chair.

NV was supported by the Cell and Tissue Engineering NIH Biotechnology Training Grant (T32 GM-008433) and a supplement fund to the NIH grant HL119798.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cardiac & Cardiovascular Systems
  • Cardiovascular System & Cardiology
  • cyclic stretch
  • HIF1A
  • PX-478
  • aortic valve
  • calcification
  • INDUCIBLE FACTOR-I
  • TRANSCATHETER
  • REPLACEMENT
  • DISEASE
  • MECHANISMS
  • STENOSIS

HIF1A inhibitor PX-478 reduces pathological stretch-induced calcification and collagen turnover in aortic valve

Tools:

Journal Title:

FRONTIERS IN CARDIOVASCULAR MEDICINE

Volume:

Volume 9

Publisher:

, Pages 1002067-1002067

Type of Work:

Article | Final Publisher PDF

Abstract:

HIF1A is significantly upregulated in calcified human aortic valves (AVs). Furthermore, HIF1A inhibitor PX-478 was shown to inhibit AV calcification under static and disturbed flow conditions. Since elevated stretch is one of the major mechanical stimuli for AV calcification, we investigated the effect of PX-478 on AV calcification and collagen turnover under a pathophysiological cyclic stretch (15%) condition. Porcine aortic valve (PAV) leaflets were cyclically (1 Hz) stretched at 15% for 24 days in osteogenic medium with or without PX-478. In addition, PAV leaflets were cyclically stretched at a physiological (10%) and 15% for 3 days in regular medium to assess its effect of on HIF1A mRNA expression. It was found that 100 μM (high concentration) PX-478 could significantly inhibit PAV calcification under 15% stretch, whereas 50 μM (moderate concentration) PX-478 showed a modest inhibitory effect on PAV calcification. Nonetheless, 50 μM PX-478 significantly reduced PAV collagen turnover under 15% stretch. Surprisingly, it was observed that cyclic stretch (15% vs. 10%) did not have any significant effect on HIF1A mRNA expression in PAV leaflets. These results suggest that HIF1A inhibitor PX-478 may impart its anti-calcific and anti-matrix remodeling effect in a stretch-independent manner.

Copyright information:

© 2022 Salim, Villa-Roel, Vogel, Jo and Yoganathan.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/rdf).
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