Department of Spine Surgery, the First Affiliated Hospital and Orthopedic Research Institute of Sun Yat-sen University, Guangzhou, China.
Department of Pediatric Intensive Care Unit, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Spine (Phila Pa 1976). 2019 Sep;44(18):E1053-E1062. doi: 10.1097/BRS.0000000000003059.
An in vivo and in vitro study of the correlation between Paraoxonase 1 (PON1) and intervertebral disc degeneration (IVDD).
The aim of this study is to clarify the expression and role of PON1 on the process of IVDD.
IVDD is responsible for most of the spinal degenerative diseases. Inflammation and oxidative stress can deteriorate the living environment of nucleus pulposus (NP) cells, leading to IVDD. PON1 is an enzyme reported to have anti-inflammatory and anti-oxidative effects. There is no study about the correlation of PON1 expression with IVDD.
Immunohistochemical (IHC), hematoxylin and eosin (H&E) staining, and Western blot examined the expression of PON1 in 88 human disc samples (male: female 43: 45) and rat models (n = 5 each group). The level of PON1 is measured in the tumor necrosis factor (TNF)-α and oxidative stress (H2O2)-induced degenerative NP cell models using Western blot and reverse transcription-polymerase chain reaction (RT-qPCR). The TNF-α, interleukin (IL)-1β, Mito superoxide (SOX), aggrecan, and collagen II are detected in nucleus pulposus (NP) cells transfected with si-RNA of PON1 using Enzyme-Linked Immunosorbent Assay (ELISA), mitoSOX staining Western blot, and RT-qPCR.
The expression of PON1 is significantly suppressed in human and rat degenerative intervertebral discs. The level of PON1 is significantly decreased in TNF-α and oxidative stress (H2O2)-induced degenerative NP cell models. ELISA results show that the level of TNF-α and IL-1β obviously increased; Mito SOX staining indicates that the Mito SOX fluorescence significantly increased, and the expression of aggrecan and collagen reduced in NP cells transfected with si-RNA of PON1.
Our study indicates that low PON1 expression is predictive of severe IVDD; PON1 plays an important role of keeping the homeostatic balance of intervertebral discs, and therapeutic approach regarding PON1 may be helpful to alleviate IVDD in the future.
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对人椎间盘中过氧化物酶 1(PON1)与椎间盘退变(IVDD)之间的相关性进行体内和体外研究。
本研究旨在阐明 PON1 在 IVDD 过程中的表达和作用。
IVDD 是大多数脊柱退行性疾病的原因。炎症和氧化应激会恶化髓核(NP)细胞的生存环境,导致 IVDD。PON1 是一种具有抗炎和抗氧化作用的酶。目前尚无关于 PON1 表达与 IVDD 相关性的研究。
免疫组织化学(IHC)、苏木精和伊红(H&E)染色和 Western blot 检测了 88 个人椎间盘样本(男:女 43:45)和大鼠模型(每组 5 只)中 PON1 的表达。采用 Western blot 和逆转录-聚合酶链反应(RT-qPCR)检测 TNF-α和氧化应激(H2O2)诱导的退变 NP 细胞模型中 PON1 的水平。采用酶联免疫吸附试验(ELISA)、mitoSOX 染色 Western blot 和 RT-qPCR 检测转染 PON1 siRNA 的 NP 细胞中 TNF-α、白细胞介素(IL)-1β、Mito SOX、聚集蛋白聚糖和胶原 II 的水平。
PON1 的表达在人退变椎间盘和大鼠退变椎间盘中有明显抑制。TNF-α和氧化应激(H2O2)诱导的退变 NP 细胞模型中 PON1 的水平明显降低。ELISA 结果显示 TNF-α和 IL-1β水平明显升高;mitoSOX 染色表明 Mito SOX 荧光明显增强,转染 PON1 siRNA 的 NP 细胞中聚集蛋白聚糖和胶原表达降低。
本研究表明,PON1 低表达预示着严重的 IVDD;PON1 在维持椎间盘的内稳态平衡中发挥着重要作用,针对 PON1 的治疗方法可能有助于减轻未来的 IVDD。
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