Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs

Vertebral osteomyelitis (VO) is an infection of the spine mainly caused by bacterial pathogens. The pathogenesis leading to destruction of intervertebral discs (IVDs) and adjacent vertebral bodies (VBs) is poorly described. The present study aimed at investigating the connection between infection an...

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Autores principales: S Lang, M Loibl, J Gläsner, M Simon, M Rupp, S Grad, C Neumann, V Alt, A Gessner, F Hanses
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Publicado: AO Research Institute Davos 2021
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spelling oai:doaj.org-article:e5c469cfa614454f88a1012c713f897f2021-11-30T13:28:41ZVertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs10.22203/eCM.v042a271473-2262https://doaj.org/article/e5c469cfa614454f88a1012c713f897f2021-11-01T00:00:00Zhttps://www.ecmjournal.org/papers/vol042/pdf/v042a27.pdfhttps://doaj.org/toc/1473-2262Vertebral osteomyelitis (VO) is an infection of the spine mainly caused by bacterial pathogens. The pathogenesis leading to destruction of intervertebral discs (IVDs) and adjacent vertebral bodies (VBs) is poorly described. The present study aimed at investigating the connection between infection and bone/disc metabolism in VO patients. 14 patients with VO (infection group) and 14 patients with burst fractures of the spine (fracture group; control) were included prospectively. Tissue biopsies from affected IVDs and adjacent VBs were analysed by RT-qPCR for mRNA-expression levels of 18 target genes including chemokines, adipokines and genes involved in bone metabolism. Most importantly, the receptor activator of NF-κB/osteoprotegerin (RANK/OPG) expression ratio was drastically elevated in both VBs and IVDs of the infection group. In parallel, expression of genes of the prostaglandin-E2-dependent prostanoid system was induced. Such genes regulate tissue degradation processes via the triad OPG/RANK/RANKL as well as via the chemokines IL-8 and CCL-20, whose expression was also found to be increased upon infection. The gene expression of the adipokine leptin, which promotes inflammatory tissue degradation, was higher in IVD tissue of the infection group, whereas the transcription of omentin and resistin genes, whose functions are largely unknown in the context of infectious diseases, was lower in infected VBs. In summary, similar expression patterns of pro-inflammatory cytokines and pro-osteoclastogenic factors were identified in VBs and IVDs of patients suffering from VO. This suggests that common immuno-metabolic pathways are involved in the mechanisms leading to tissue degradation in VBs and IVDs during VO.S LangM LoiblJ GläsnerM SimonM Rupp S GradC NeumannV AltA GessnerF Hanses AO Research Institute Davosarticlevertebral osteomyelitissignalling molecules-cytokinesadipokinescells/tissues-intervertebral discinfection-in vivospine-vertebral bodyosteoimmunitySurgeryRD1-811Diseases of the musculoskeletal systemRC925-935ENEuropean Cells & Materials, Vol 42, Pp 438-451 (2021)
institution DOAJ
collection DOAJ
language EN
topic vertebral osteomyelitis
signalling molecules-cytokines
adipokines
cells/tissues-intervertebral disc
infection-in vivo
spine-vertebral body
osteoimmunity
Surgery
RD1-811
Diseases of the musculoskeletal system
RC925-935
spellingShingle vertebral osteomyelitis
signalling molecules-cytokines
adipokines
cells/tissues-intervertebral disc
infection-in vivo
spine-vertebral body
osteoimmunity
Surgery
RD1-811
Diseases of the musculoskeletal system
RC925-935
S Lang
M Loibl
J Gläsner
M Simon
M Rupp
S Grad
C Neumann
V Alt
A Gessner
F Hanses
Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
description Vertebral osteomyelitis (VO) is an infection of the spine mainly caused by bacterial pathogens. The pathogenesis leading to destruction of intervertebral discs (IVDs) and adjacent vertebral bodies (VBs) is poorly described. The present study aimed at investigating the connection between infection and bone/disc metabolism in VO patients. 14 patients with VO (infection group) and 14 patients with burst fractures of the spine (fracture group; control) were included prospectively. Tissue biopsies from affected IVDs and adjacent VBs were analysed by RT-qPCR for mRNA-expression levels of 18 target genes including chemokines, adipokines and genes involved in bone metabolism. Most importantly, the receptor activator of NF-κB/osteoprotegerin (RANK/OPG) expression ratio was drastically elevated in both VBs and IVDs of the infection group. In parallel, expression of genes of the prostaglandin-E2-dependent prostanoid system was induced. Such genes regulate tissue degradation processes via the triad OPG/RANK/RANKL as well as via the chemokines IL-8 and CCL-20, whose expression was also found to be increased upon infection. The gene expression of the adipokine leptin, which promotes inflammatory tissue degradation, was higher in IVD tissue of the infection group, whereas the transcription of omentin and resistin genes, whose functions are largely unknown in the context of infectious diseases, was lower in infected VBs. In summary, similar expression patterns of pro-inflammatory cytokines and pro-osteoclastogenic factors were identified in VBs and IVDs of patients suffering from VO. This suggests that common immuno-metabolic pathways are involved in the mechanisms leading to tissue degradation in VBs and IVDs during VO.
format article
author S Lang
M Loibl
J Gläsner
M Simon
M Rupp
S Grad
C Neumann
V Alt
A Gessner
F Hanses
author_facet S Lang
M Loibl
J Gläsner
M Simon
M Rupp
S Grad
C Neumann
V Alt
A Gessner
F Hanses
author_sort S Lang
title Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
title_short Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
title_full Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
title_fullStr Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
title_full_unstemmed Vertebral osteomyelitis is characterised by increased RANK/OPG and RANKL/OPG expression ratios in vertebral bodies and intervertebral discs
title_sort vertebral osteomyelitis is characterised by increased rank/opg and rankl/opg expression ratios in vertebral bodies and intervertebral discs
publisher AO Research Institute Davos
publishDate 2021
url https://doaj.org/article/e5c469cfa614454f88a1012c713f897f
work_keys_str_mv AT slang vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT mloibl vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT jglasner vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT msimon vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT mrupp vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT sgrad vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT cneumann vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT valt vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT agessner vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
AT fhanses vertebralosteomyelitisischaracterisedbyincreasedrankopgandranklopgexpressionratiosinvertebralbodiesandintervertebraldiscs
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