Wu Xinghuo, Liu Wei, Duan Zhenfeng, Gao Yong, Li Shuai, Wang Kun, Song Yu, Shao Zengwu, Yang Shuhua, Yang Cao
Department of Orthopaedic Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Department of Orthopaedic Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Sci Rep. 2016 Jul 27;6:30563. doi: 10.1038/srep30563.
Protease nexin-1 (PN-1) is a serine protease inhibitor belonging to the serpin superfamily. This study was undertaken to investigate the regulatory role of PN-1 in the pathogenesis of intervertebral disk (IVD) degeneration. Expression of PN-1 was detected in human IVD tissue of varying grades. Expression of both PN-1 mRNA and protein was significantly decreased in degenerated IVD, and the expression levels of PN-1 were correlated with the grade of disc degeneration. Moreover, a decrease in PN-1 expression in primary NP cells was confirmed. On induction by IL-1β, the expression of PN-1 in NP cells was decreased at day 7, 14, and 21, as shown by western blot analysis and immunofluorescence staining. PN-1 administration decreased IL-1β-induced MMPs and ADAMTS production and the loss of Agg and Col II in NP cell cultures through the ERK1/2/NF-kB signaling pathway. The changes in PN-1 expression are involved in the pathogenesis of IVD degeneration. Our findings indicate that PN-1 administration could antagonize IL-1β-induced MMPs and ADAMTS, potentially preventing degeneration of IVD tissue. This study also revealed new insights into the regulation of PN-1 expression via the ERK1/2/NF-kB signaling pathway and the role of PN-1 in the pathogenesis of IVD degeneration.
蛋白酶抑制因子-1(PN-1)是一种属于丝氨酸蛋白酶抑制剂超家族的丝氨酸蛋白酶抑制剂。本研究旨在探讨PN-1在椎间盘(IVD)退变发病机制中的调节作用。在不同退变程度的人IVD组织中检测到PN-1的表达。退变的IVD中PN-1 mRNA和蛋白的表达均显著降低,且PN-1的表达水平与椎间盘退变程度相关。此外,还证实了原代髓核细胞中PN-1表达的降低。经白细胞介素-1β(IL-1β)诱导后,通过蛋白质印迹分析和免疫荧光染色显示,在第7天、14天和21天,髓核细胞中PN-1的表达降低。给予PN-1可通过细胞外信号调节激酶1/2(ERK1/2)/核因子κB(NF-κB)信号通路降低IL-1β诱导的基质金属蛋白酶(MMPs)和含血小板解聚蛋白基序的金属蛋白酶(ADAMTS)的产生以及髓核细胞培养物中聚集蛋白聚糖(Agg)和Ⅱ型胶原(Col II)的丢失。PN-1表达的变化参与了IVD退变的发病机制。我们的研究结果表明,给予PN-1可拮抗IL-1β诱导的MMPs和ADAMTS,可能预防IVD组织退变。本研究还揭示了通过ERK1/2/NF-κB信号通路调节PN-1表达以及PN-1在IVD退变发病机制中的作用的新见解。