Pain mediator NGF improves chondrocyte extracellular matrix synthesis via PI3K/AKT pathway.

IF 2.8 3区 医学 Q1 ORTHOPEDICS Journal of Orthopaedic Surgery and Research Pub Date : 2025-02-27 DOI:10.1186/s13018-025-05503-x
Mengling Wang, Jie Lian, Maoqing Ye, Bingchen An
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Abstract

Objectives: Nerve growth factor (NGF) is a key mediator in osteoarthritis pain signaling. Clinical studies revealed that anti-NGF antibodies are often accompanied by progressively worsening cartilage degeneration, although they exhibit significant analgesic effects. However, the relationship between NGF expression and cartilage destruction remains unclear. Our study aimed to investigate the effects of NGF on chondrocytes and to elucidate the underlying mechanisms involved.

Methods: The ATDC5 cells were induced to differentiate into chondrocytes and stimulated with NGF at different concentrations (0.5-10 ng/mL). The cell counting kit-8 assay (CCK-8) was used to measure the effects of NGF on chondrocyte proliferation. Chondrocytes were subsequently stimulated with varying doses of NGF to identify the expression levels of the extracellular matrix. Chondrocytes were pretreated with GNF5837 (a tropomyosin receptor kinase A inhibitor) or LY294002 (a phosphoinositide 3-kinase inhibitor) before exposure to 5 ng/mL NGF to analyze associated signaling pathways. Western blotting and immunofluorescence staining were employed to analyze expression of related proteins.

Results: Alcian blue, toluidine blue staining, and type II collagen immunofluorescence staining demonstrated that ATDC5 cells differentiated into functional chondrocytes after 14 days of chondrogenic induction. The CCK-8 assay confirmed that cell proliferation was unaffected. NGF (0.5-5 ng/mL) was found to enhance chondrocyte matrix synthesis in a dose-dependent fashion, particularly in the expression of aggrecan, type II collagen, Sox9, and through the activation of the PI3K/AKT signaling pathway. The highest promoting effects were exhibited at 5 ng/mL of NGF. Further analysis indicated that GNF5837 (TRKA inhibitor) or LY294002 (PI3K inhibitor) could reverse the protective effects of NGF on chondrocyte matrix synthesis.

Conclusion: Our study identified a potentially beneficial role of NGF at concentrations of 0.5-5 ng/mL in chondrocytes, enhancing extracellular matrix synthesis, with significant involvement of the PI3K/AKT signaling pathway in this process.

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疼痛介质NGF通过PI3K/AKT通路促进软骨细胞外基质合成。
目的:神经生长因子(NGF)是骨关节炎疼痛信号的关键介质。临床研究表明,抗ngf抗体通常伴随着软骨退行性变的逐渐恶化,尽管它们具有显著的镇痛作用。然而,NGF表达与软骨破坏之间的关系尚不清楚。本研究旨在探讨NGF对软骨细胞的影响,并阐明其潜在机制。方法:采用不同浓度(0.5 ~ 10 ng/mL)的NGF刺激ATDC5细胞向软骨细胞分化。采用细胞计数试剂盒-8法(CCK-8)检测NGF对软骨细胞增殖的影响。随后用不同剂量的NGF刺激软骨细胞,以确定细胞外基质的表达水平。软骨细胞在暴露于5 ng/mL NGF之前,用GNF5837(原肌球蛋白受体激酶a抑制剂)或LY294002(磷酸肌肽3激酶抑制剂)预处理,分析相关的信号通路。Western blotting和免疫荧光染色分析相关蛋白的表达。结果:阿利新蓝、甲苯胺蓝染色和II型胶原免疫荧光染色显示,ATDC5细胞在诱导成软骨14天后分化为功能性软骨细胞。CCK-8检测证实细胞增殖不受影响。研究发现,NGF (0.5-5 ng/mL)以剂量依赖性的方式增强软骨细胞基质的合成,特别是在聚集蛋白、II型胶原、Sox9的表达中,并通过激活PI3K/AKT信号通路。NGF浓度为5 ng/mL时,促进作用最大。进一步分析表明,GNF5837 (TRKA抑制剂)或LY294002 (PI3K抑制剂)可逆转NGF对软骨细胞基质合成的保护作用。结论:我们的研究发现,浓度为0.5-5 ng/mL的NGF在软骨细胞中具有潜在的有益作用,可以促进细胞外基质的合成,并显著参与PI3K/AKT信号通路在这一过程中。
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来源期刊
CiteScore
4.10
自引率
7.70%
发文量
494
审稿时长
>12 weeks
期刊介绍: Journal of Orthopaedic Surgery and Research is an open access journal that encompasses all aspects of clinical and basic research studies related to musculoskeletal issues. Orthopaedic research is conducted at clinical and basic science levels. With the advancement of new technologies and the increasing expectation and demand from doctors and patients, we are witnessing an enormous growth in clinical orthopaedic research, particularly in the fields of traumatology, spinal surgery, joint replacement, sports medicine, musculoskeletal tumour management, hand microsurgery, foot and ankle surgery, paediatric orthopaedic, and orthopaedic rehabilitation. The involvement of basic science ranges from molecular, cellular, structural and functional perspectives to tissue engineering, gait analysis, automation and robotic surgery. Implant and biomaterial designs are new disciplines that complement clinical applications. JOSR encourages the publication of multidisciplinary research with collaboration amongst clinicians and scientists from different disciplines, which will be the trend in the coming decades.
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