4.4 Article

Targeted screening of inflammatory mediators in spontaneous degenerative disc disease in dogs reveals an upregulation of the tumor necrosis superfamily

Journal

JOR SPINE
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/jsp2.1292

Keywords

back pain; degenerative disc disease; dog; inflammation; nerve growth factor; RANKL; tumor necrosis factor superfamily

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This study investigated the expression of inflammatory mediators in degenerated ligamentum flavum (LF) and intervertebral disc (IVD) and identified potential treatment targets. Various TNFSF members were significantly regulated in the degenerated IVD, while TNFSF genes were not significantly affected in the degenerated LF. The study also found changes in the expression of NGF and RANKL proteins.
Background: The regulation of inflammatory mediators in the degenerating intervertebral disc (IVD) and corresponding ligamentum flavum (LF) is a topic of emerging interest. The study aimed to investigate the expression of a broad array of inflammatory mediators in the degenerated LF and IVD using a dog model of spontaneous degenerative disc disease (DDD) to determine potential treatment targets. Methods: LF and IVD tissues were collected from 22 normal dogs (Pfirrmann grades I and II) and 18 dogs affected by DDD (Pfirrmann grades III and IV). A qPCR gene array was used to investigate the expression of 80 inflammatory genes for LF and IVD tissues, whereafter targets of interest were investigated in additional tissue samples using qPCR, western blot (WB), and immunohistochemistry. Results: Tumor necrosis factor superfamily (TNFSF) signaling was identified as a regulated pathway in DDD, based on the significant regulation (n-fold +/- SD) of various TNFSF members in the degenerated IVD, including nerve growth factor (NGF; -8 +/- 10), CD40LG (464 +/- 442), CD70 (341 +/- 336), TNFSF Ligand 10 (9 +/- 8), and RANKL/TNFSF Ligand 11 (85 +/- 74). In contrast, TNFSF genes were not significantly affected in the degenerated LF compared to the control LF. Protein expression of NGF (WB) was significantly upregulated in both the degenerated LF (4.4 +/- 0.5) and IVD (11.3 +/- 5.6) compared to the control group. RANKL immunopositivity was significantly upregulated in advanced stages of degeneration (Thompson grades IV and V) in the nucleus pulposus and annulus fibrosus of the IVD, but not in the LF. Conclusions: DDD involves a significant upregulation of various TNFSF members, with tissue-specific expression profiles in LF and IVD tissues. The differential involvement of TNFSF members within multiple spinal tissues from the same individual provides new insights into the inflammatory processes involved in DDD and may provide a basis to formulate hypotheses for the determination of potential treatment targets.

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