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Targeting Sphingosine-1-Phosphate Signaling to Prevent the Progression of Aortic Valve Disease

  • Marcel Benkhoff
  • , Maike Barcik
  • , Philipp Mourikis
  • , Jana Dahlmanns
  • , Paulina Kahmann
  • , Philipp Wollnitzke
  • , Moritz Hering
  • , Tim Huckenbeck
  • , Julia Hoppe
  • , Nina Semleit
  • , Jennifer Deister-Jonas
  • , Saif Zako
  • , Jasmin Seel
  • , Cristina Coman
  • , Mareike Barth
  • , Mareike Cramer
  • , Carolin Helten
  • , Laura Wildeis
  • , Hao Hu
  • , Gabrielle Al-Kassis
  • Daniel Metzen, Julia Hesse, Jessica Weber, Lisa Dannenberg, Payam Akhyari, Artur Lichtenberg, Christine Quast, Norbert Gerdes, Tobias Zeus, Oliver Borst, Malte Kelm, Tobias Petzold, Robert Ahrends, Bodo Levkau, Amin Polzin (Korresp. Autor*in)

Veröffentlichungen: Beitrag in Fachzeitschrift › Artikel › Peer Reviewed

Abstract

BACKGROUND: Aortic valve disease (AVD) is associated with high mortality and morbidity. To date, there is no pharmacological therapy available to prevent AVD progression. Because valve calcification is the hallmark of AVD and S1P (sphingosine-1-phosphate) plays an important role in osteogenic signaling, we examined the role of S1P signaling in aortic stenosis disease. METHODS: AVD progression and its consequences for cardiac function were examined in a murine wire injury-induced AVD model with and without pharmacological and genetic modulation of S1P production, degradation, and receptor signaling. S1P was measured by LC-MS. Calcification of valvular interstitial cells and their response to biomechanical stress were analyzed in the context of S1P signaling. Human explanted aortic valves from patients undergoing aortic valve replacement and cardiovascular magnetic resonance imaging were analyzed for S1P by LC-MS. RESULTS: Raising S1P concentrations in mice with injury-induced AVD by pharmacological inhibition of its sole degrading enzyme S1P lyase vastly enhanced AVD progression and impaired cardiac function resembling human disease. In contrast, low S1P levels caused by SphK1 (sphingosine kinase 1) deficiency potently attenuated AVD progression. We found S1P/S1PR2 (S1P receptor 2) signaling to be responsible for the adverse S1P effect because S1PR2-deficient mice were protected against AVD progression and its deterioration by high S1P. It is important to note that pharmacological S1PR2 inhibition administered after wire injury successfully prevented AVD development. Mechanistically, biomechanical stretch stimulated S1P production by SphK1 in human valvular interstitial cells as measured by C17-S1P generation, whereas S1P/S1PR2 signaling induced their osteoblastic differentiation and calcification through osteogenic RUNX2/OPG signaling and the GSK3β-Wnt-β-catenin pathway. In patients with AVD, stenotic valves exposed to high wall shear stress had higher S1P content and increased SphK1 expression. CONCLUSIONS: Increased systemic or local S1P levels lead to increased valvular calcification. S1PR2 antagonists and SphK1 inhibitors may offer feasible pharmacological approaches to human AVD in prophylactic, disease-modifying or relapse-preventing manners.

OriginalspracheEnglisch
Seiten (von - bis)333-347
Seitenumfang15
FachzeitschriftCirculation
Jahrgang151
Ausgabenummer4
DOIs
PublikationsstatusVeröffentlicht - 28 Jan. 2025

Fördermittel

The authors thank Julia Odendahl for experimental support. We acknowledge the support of the Susanne-Bunnenberg-Stiftung at the D\u00FCsseldorf Heart Center. M. Benkhoff, M. Barcik, M.K., B.L., and A.P. designed the study, analyzed the data, and drafted the article. M. Barcik and J.S. performed histological analyses. M. Benkhoff, M. Barcik, and H.H. performed murine experiments including analysis of echocardiographic data. P.W., N.S., and C.C. performed S1P measurements. H.H. measured arterial blood pressure in mice. L.W. did the quantification of osteogenic mediators in plasma. G.A. conducted flow-cytometry analysis. M.C., S.Z., and C.H. conducted, analyzed, and interpreted CMR data. J.D. and P.K. performed polymerase chain reaction analyses. P.M., J.D.-J., J.H., M.H., and T.H. conducted cell culture experiments on human VICs including C17 sphingosine assay and cell stretching. M. Barcik provided human valvular tissue and help with analyzing and interpretation of corresponding data. J.H. did the immunoblotting experiments. D.M. aided in statistical analysis and figure conception. J.W. and L.D. collected human data and helped to analyze and interpret it. Together with M. Benkhoff and A.P., P.A., A.L., C.Q., N.G., T.Z., O.B., T.P., and R.A. revised and discussed all data. All authors critically reviewed and approved the final version of the article. This work was supported by the Deutsche Forschungsgemeinschaft (German Research Foundation) grant No. 530690968 to M.B.; 236177352-SFB1116, TP B11 to A.P. and B.L.; TP B09 to N.G.; TP B6 and B12 to M.K.; 493400536, 413659045, and 510844896 to A.P.; PE2704/3-1, PE2704/4-1, and PE2704/5-1 to T.P.; and 397484323-TRR259, TP B10 to B.L. This study was also supported by the German Heart Foundation grant No. F/32/22 to A.P. and K/24/23 to J.D., and by the Medical Faculty of Heinrich Heine University (grant No. 18-2019 to A.P. and 2021-01 to P.M.). This work was supported by the Deutsche Forschungsgemeinschaft (German Research Foundation) grant No. 530690968 to M.B.; 236177352-SFB1116, TP B11 to A.P. and B.L.; TP B09 to N.G.; TP B6 and B12 to M.K.; 493400536, 413659045, and 510844896 to A.P.; PE2704/3-1, PE2704/4-1, and PE2704/5-1 to T.P.; and 397484323-TRR259, TP B10 to B.L. This study was also supported by the German Heart Foundation grant No. F/32/22 to A.P. and K/24/23 to J.D., and by the Medical Faculty of Heinrich Heine University (grant No. 18-2019 to A.P. and 2021-01 to P.M.).

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gesundheit und Wohlergehen
    SDG 3 – Gesundheit und Wohlergehen

ÖFOS 2012

  • 301305 Medizinische Chemie
  • 301304 Medizinische Biologie
  • 302032 Kardiologie

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