Effects of GDF6 on active protein synthesis by cells of degenerated intervertebral disc.

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY European Spine Journal Pub Date : 2025-06-01 Epub Date: 2025-02-08 DOI:10.1007/s00586-025-08715-1
Vivian Tam, Neha Chopra, Stone Sima, Peikai Chen, Rakesh Sharma, Danny Chan, Ashish Diwan
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Abstract

Introduction: Intervertebral disc degeneration (IVD) is a leading cause of low back pain, a prevalent musculoskeletal condition. IVD degeneration is characterized by the degradation of nucleus pulposus (NP), annulus fibrosus (AF), and cartilage endplates (EP). Growth Differentiation Factor 6 (GDF6), part of the bone morphogenetic protein family, has demonstrated potential in maintaining disc integrity. However, its precise role in cellular protein synthesis during IVD degeneration remains unclear.

Methods: This study employed Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) to investigate the effects of GDF6 on protein synthesis in NP, AF, and EP cells isolated from degenerated human IVDs. Cells were cultured in SILAC media with and without GDF6 treatment. The proteomic profiles were analyzed via mass spectrometry, comparing newly synthesized "heavy" proteins with pre-existing "light" proteins.

Results: GDF6 treatment altered protein synthesis in degenerated IVD cells. In NP cells, GDF6 reduced the synthesis of matrisome proteins, including collagens and proteoglycans, while promoting proteins associated with ECM stability, such as LOX, PCOLCE and HAPLN1/3. AF cells demonstrated an upregulation of ECM-stabilizing proteins like POSTN and FMOD. EP cells showed minimal changes, but GDF6 enhanced the synthesis of collagen type II, suggesting improved ECM integrity. Secretome analysis revealed that GDF6 modulated extracellular signalling by promoting ECM-stabilizing proteins and reducing inflammatory markers.

Conclusion: GDF6 exerts compartment-specific effects on protein synthesis in degenerated IVDs, promoting ECM stability, reducing fibrosis, and potentially preserving hydration. These findings support the potential of GDF6 as a therapeutic agent in treating IVD degeneration, particularly in NP-targeted therapies. Future studies should optimize GDF6 dosing and delivery to maximize its regenerative potential.

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GDF6对退变椎间盘细胞合成活性蛋白的影响。
简介:椎间盘退变(IVD)是腰痛的主要原因,腰痛是一种普遍的肌肉骨骼疾病。IVD退变的特征是髓核(NP)、纤维环(AF)和软骨终板(EP)的退化。生长分化因子6 (GDF6)是骨形态发生蛋白家族的一员,具有维持椎间盘完整性的潜力。然而,其在IVD变性过程中细胞蛋白合成中的确切作用尚不清楚。方法:采用细胞培养氨基酸稳定同位素标记法(SILAC)研究GDF6对人源性ivd退行性NP、AF和EP细胞蛋白质合成的影响。细胞在加GDF6和不加GDF6的SILAC培养基中培养。通过质谱分析蛋白质组学图谱,将新合成的“重”蛋白与已有的“轻”蛋白进行比较。结果:GDF6处理改变了变性IVD细胞的蛋白质合成。在NP细胞中,GDF6减少了基质蛋白的合成,包括胶原和蛋白聚糖,同时促进了与ECM稳定性相关的蛋白,如LOX、PCOLCE和hapln /3。AF细胞表现出ecm稳定蛋白如POSTN和FMOD的上调。EP细胞变化不大,但GDF6增强了II型胶原的合成,表明ECM的完整性得到改善。分泌组分析显示,GDF6通过促进ecm稳定蛋白和减少炎症标志物来调节细胞外信号传导。结论:GDF6对退行性ivd的蛋白质合成具有室特异性作用,促进ECM稳定性,减少纤维化,并可能保持水合作用。这些发现支持GDF6作为治疗IVD变性的药物的潜力,特别是在np靶向治疗中。未来的研究应优化GDF6的剂量和递送,以最大限度地发挥其再生潜力。
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来源期刊
European Spine Journal
European Spine Journal 医学-临床神经学
CiteScore
4.80
自引率
10.70%
发文量
373
审稿时长
2-4 weeks
期刊介绍: "European Spine Journal" is a publication founded in response to the increasing trend toward specialization in spinal surgery and spinal pathology in general. The Journal is devoted to all spine related disciplines, including functional and surgical anatomy of the spine, biomechanics and pathophysiology, diagnostic procedures, and neurology, surgery and outcomes. The aim of "European Spine Journal" is to support the further development of highly innovative spine treatments including but not restricted to surgery and to provide an integrated and balanced view of diagnostic, research and treatment procedures as well as outcomes that will enhance effective collaboration among specialists worldwide. The “European Spine Journal” also participates in education by means of videos, interactive meetings and the endorsement of educative efforts. Official publication of EUROSPINE, The Spine Society of Europe
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