Analysis of Intervertebral Disc Degeneration Induced by Endplate Drilling or Needle Puncture in Complement C6-Sufficient and C6-Deficient Rabbits

Author:

Kuhn Amelie1,Huber-Lang Markus2,Weckbach Sebastian3,Riegger Jana1ORCID,Teixeira Graciosa Q.4ORCID,Rasche Volker56ORCID,Fiedler Jörg1ORCID,Neidlinger-Wilke Cornelia4ORCID,Brenner Rolf E.1

Affiliation:

1. Division for Biochemistry of Joint and Connective Tissue Diseases, Department of Orthopedics, Ulm University, 89081 Ulm, Germany

2. Institute of Clinical and Experimental Trauma-Immunology, University Hospital Ulm, Ulm University, 89081 Ulm, Germany

3. Department of Orthopedic Surgery, RKU, Ulm University, 89081 Ulm, Germany

4. Institute of Orthopedic Research and Biomechanics, Trauma Research Centre, Ulm University, 89081 Ulm, Germany

5. Department of Internal Medicine II, Ulm University, 89081 Ulm, Germany

6. Core Facility Small Animal Imaging (CF-SANI), Ulm University, 89081 Ulm, Germany

Abstract

Previous studies indicate an implication of the terminal complement complex (TCC) in disc degeneration (DD). To investigate the functional role of TCC in trauma-induced DD in vivo, the model of endplate (EP) drilling was first applied in rabbits using a C6-deficient rabbit strain in which no TCC formation was possible. In parallel the model of needle puncture was investigated. Using a minimally invasive surgical intervention, lumbar rabbit intervertebral discs (IVDs) were treated with EP drilling or needle puncture. Degenerative effects of both surgical interventions were assessed by Pfirrmann grading and T2 quantification of the IVDs based on high-resolution MRI (11.7 T), as well as radiographic determination of disc height index. Pfirrmann grading indicated significant degenerative effects after EP drilling. Contrary to our assumption, no evidence was found that the absence of TCC formation in C6-deficient rabbits reduces the development of DD compared to C6-sufficient animals. EP drilling was proven to be suitable for application in rabbits. However, results of the present study do not provide clear evidence of a central functional role of TCC within DD and suggest that TCC deposition in DD patients may be primarily considered as a marker of complement activation during DD progression.

Funder

German Research Foundation

European Social Fund

Ministry of Science, Research and Arts Baden-Württemberg

Publisher

MDPI AG

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