PACAP Inhibits TNF-α- Induced Senescence in Primary Chondrocytes by SIRT3: An Implication in Osteoarthritis.

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Xuewu Zhou, Kangquan Shou, Hao Yao
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Abstract

Osteoarthritis (OA) is a degenerative joint disease closely associated with aging, in which chondrocyte senescence plays a critical role in cartilage degradation. Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide known for its anti-inflammatory and cytoprotective effects; however, its role in chondrocyte senescence remains poorly understood. This study investigated the protective effects of PACAP38 on tumour necrosis factor-α (TNF-α)- induced chondrocyte senescence and the underlying mechanisms. Intracellular reactive oxygen species (ROS) levels were measured using 2',7'-dichlorodihydrofluorescein diacetate (DCFH-DA) staining, oxidative DNA damage was assessed by 8-hydroxy-2'-deoxyguanosine (8-OHdG) enzyme-linked immunosorbent assay (ELISA), and senescence markers were evaluated by senescence-associated β-galactosidase (SA-β-Gal) staining, telomerase activity assay, and telomere length analysis. Gene and protein expression were examined via real-time polymerase chain reaction (PCR) and Western blotting. We found that PACAP type I receptor (PAC1R), the receptor for PACAP, was expressed in both murine and human chondrocytes and was downregulated by TNF-α stimulation. PACAP38 treatment significantly reduced ROS and 8-OHdG levels, restored telomerase activity and telomere length, and decreased SA-β-Gal activity. Mechanistically, PACAP38 upregulated sirtuin 3 (SIRT3), a mitochondrial deacetylase that regulates oxidative stress and metabolism, while suppressing acetylated p53 (ac-p53) and plasminogen activator inhibitor-1 (PAI-1) expression. Furthermore, PACAP38 reversed TNF-α-induced dephosphorylation of AMP-activated protein kinase alpha (AMPK-α) and its downstream target acetyl-CoA carboxylase (ACC). Importantly, inhibition of AMPK by compound C abolished these protective effects, confirming the essential role of the AMPK-SIRT3 signalling pathway. In conclusion, our findings demonstrate that PACAP38 mitigates TNF-α-induced chondrocyte senescence via activation of the AMPK-SIRT3 signalling axis, suggesting a potential therapeutic strategy for OA.

PACAP通过SIRT3抑制TNF-α诱导的原发性软骨细胞衰老:对骨关节炎的影响。
骨关节炎(Osteoarthritis, OA)是一种与衰老密切相关的退行性关节疾病,其中软骨细胞衰老在软骨降解中起关键作用。垂体腺苷酸环化酶激活多肽(PACAP)是一种具有抗炎和细胞保护作用的神经肽;然而,其在软骨细胞衰老中的作用仍然知之甚少。本研究探讨PACAP38对肿瘤坏死因子-α (TNF-α)诱导的软骨细胞衰老的保护作用及其机制。采用2′,7′-二氯双氢荧光素(DCFH-DA)染色法检测细胞内活性氧(ROS)水平,采用8-羟基-2′-脱氧鸟苷(8-OHdG)酶联免疫吸附法(ELISA)检测DNA氧化损伤,采用衰老相关β-半乳糖苷酶(SA-β-Gal)染色、端粒酶活性测定和端粒长度分析评估衰老标志物。通过实时聚合酶链反应(PCR)和Western blotting检测基因和蛋白的表达。我们发现PACAP的受体PACAP I型受体(PAC1R)在小鼠和人软骨细胞中均有表达,并在TNF-α刺激下下调。PACAP38处理显著降低ROS和8-OHdG水平,恢复端粒酶活性和端粒长度,降低SA-β-Gal活性。在机制上,PACAP38上调sirtuin 3 (SIRT3), SIRT3是一种线粒体去乙酰化酶,调节氧化应激和代谢,同时抑制乙酰化p53 (ac-p53)和纤溶酶原激活物抑制剂-1 (PAI-1)的表达。此外,PACAP38逆转了TNF-α-诱导的amp活化蛋白激酶α (AMPK-α)及其下游靶点乙酰辅酶a羧化酶(ACC)的去磷酸化。重要的是,化合物C对AMPK的抑制消除了这些保护作用,证实了AMPK- sirt3信号通路的重要作用。总之,我们的研究结果表明,PACAP38通过激活AMPK-SIRT3信号轴来减轻TNF-α-诱导的软骨细胞衰老,提示OA的潜在治疗策略。
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来源期刊
Clinical and Experimental Pharmacology and Physiology
Clinical and Experimental Pharmacology and Physiology PHARMACOLOGY & PHARMACY-PHYSIOLOGY
自引率
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128
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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