Kuhn Amelie, Huber-Lang Markus, Weckbach Sebastian, Riegger Jana, Teixeira Graciosa Q, Rasche Volker, Fiedler Jörg, Neidlinger-Wilke Cornelia, Brenner Rolf E
Division for Biochemistry of Joint and Connective Tissue Diseases, Department of Orthopedics, Ulm University, 89081 Ulm, Germany.
Institute of Clinical and Experimental Trauma-Immunology, University Hospital Ulm, Ulm University, 89081 Ulm, Germany.
Biomedicines. 2024 Jul 30;12(8):1692. doi: 10.3390/biomedicines12081692.
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.
先前的研究表明终末补体复合物(TCC)与椎间盘退变(DD)有关。为了研究TCC在体内创伤诱导的DD中的功能作用,首先在无法形成TCC的C6缺陷兔品系中对兔应用终板(EP)钻孔模型。同时研究了针刺模型。采用微创手术干预,对兔腰椎间盘(IVD)进行EP钻孔或针刺治疗。通过基于高分辨率MRI(11.7 T)的Pfirrmann分级和IVD的T2定量以及椎间盘高度指数的影像学测定,评估两种手术干预的退变效果。Pfirrmann分级表明EP钻孔后有显著退变效应。与我们的假设相反,没有发现证据表明与C6充足的动物相比,C6缺陷兔中TCC形成的缺失会减少DD的发展。EP钻孔被证明适用于兔。然而,本研究结果并未提供明确证据证明TCC在DD中起核心功能作用,提示DD患者中TCC沉积可能主要被视为DD进展过程中补体激活的标志物。