首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Pharmacological elevation of sphingosine-1-phosphate by S1P lyase inhibition accelerates bone regeneration after post-traumatic osteomyelitis
Authors:Johannes M Wagner  Annalena Wille  Maria Fueth  Sarah Weske  Sebastian Lotzien  Felix Reinkemeier  Christoph Wallner  Alexander Sogorski  Stephanie Dittfeld  Mustafa Becerikli  Thomas A Schildhauer  Marcus Lehnhardt  Bodo Levkau  Björn Behr
Institution:1. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany;2. Institute of Molecular Medicine III, University Hospital Düsseldorf and Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany

Contribution: Data curation (equal), Formal analysis (equal), Methodology (equal), Writing - review & editing (equal);3. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Data curation (equal), Formal analysis (equal), ​Investigation (equal);4. Institute of Molecular Medicine III, University Hospital Düsseldorf and Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany

Contribution: Formal analysis (equal), ​Investigation (equal);5. Department of Trauma Surgery and General Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Conceptualization (equal), Data curation (equal), Resources (equal);6. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Conceptualization (equal), Project administration (equal), Software (equal), Supervision (equal);7. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Validation (equal), Visualization (equal), Writing - review & editing (equal);8. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: ​Investigation (equal), Methodology (equal);9. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Data curation (equal), Formal analysis (equal), Resources (equal);10. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Project administration (equal), Supervision (equal);11. Department of Trauma Surgery and General Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Project administration (equal), Supervision (equal);12. Department of Plastic Surgery, BG University Hospital Bergmannsheil Bochum, Bochum, Germany

Contribution: Conceptualization (equal), Funding acquisition (equal), Project administration (equal), Resources (equal);13. Institute of Molecular Medicine III, University Hospital Düsseldorf and Heinrich Heine Universität Düsseldorf, Düsseldorf, Germany

Contribution: Project administration (equal), Supervision (equal), Validation (equal), Writing - original draft (equal), Writing - review & editing (equal)

Abstract:Posttraumatic osteomyelitis and the ensuing bone defects are a debilitating complication after open fractures with little therapeutic options. We have recently identified potent osteoanabolic effects of sphingosine-1-phosphate (S1P) signalling and have now tested whether it may beneficially affect bone regeneration after infection. We employed pharmacological S1P lyase inhibition by 4-deoxypyrodoxin (DOP) to raise S1P levels in vivo in an unicortical long bone defect model of posttraumatic osteomyelitis in mice. In a translational approach, human bone specimens of clinical osteomyelitis patients were treated in organ culture in vitro with DOP. Bone regeneration was assessed by μCT, histomorphometry, immunohistology and gene expression analysis. The role of S1P receptors was addressed using S1PR3 deficient mice. Here, we present data that DOP treatment markedly enhanced osteogenesis in posttraumatic osteomyelitis. This was accompanied by greatly improved osteoblastogenesis and enhanced angiogenesis in the callus accompanied by osteoclast-mediated bone remodelling. We also identified the target of increased S1P to be the S1PR3 as S1PR3−/− mice showed no improvement of bone regeneration by DOP. In the human bone explants, bone mass significantly increased along with enhanced osteoblastogenesis and angiogenesis. Our data suggest that enhancement of S1P/S1PR3 signalling may be a promising therapeutic target for bone regeneration in posttraumatic osteomyelitis.
Keywords:bone regeneration  osteomyelitis  sphingosin-1-phosphate
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号