摘要
目的检测人退变颈椎间盘髓核组织的细胞凋亡率以及相关蛋白Caspase-1及IL-1β的表达。方法将30例颈椎间盘突出症患者(实验组)的间盘髓核组织和30例颈椎骨折患者(对照组)的间盘髓核组织,采用原位DNA片段末端标记(TUNEL)法和免疫组织化学方法,观察其细胞凋亡状态及Caspase-1及IL-1β的表达。结果实验组TUNEL阳性细胞率为(10.21±1.13)%,高于对照组的(6.34±1.65)%(P<0.01);实验组Caspase-1、IL-1β蛋白阳性细胞率分别为(42.31±8.08)%、(56.07±10.22)%,高于对照组的(22.06±1.28)%、(43.12±13.56)%(P<0.01)。将实验组进行Pearson相关分析,发现间盘髓核组织TUNEL阳性细胞率和Caspase-1、IL-1β阳性细胞率呈正相关,相关系数r分别为0.828和0.780(P<0.01)。结论在人退变颈椎间盘髓核中,高表达的Caspase-1、IL-1β与其细胞凋亡有关,是引起盘源性颈椎间盘退变的原因之一。
Objective To detect the apoptosis rates of degenerated human intervertebral disc cartilage endplate and nucleus pulposus cells and the related gene expressions of Caspase- 1 and IL^-1β. Methods The apoptosis state and expressions of Caspase- 1 and IL^-1β in the disc tissues of 30 patients with cervical spondylosis and 30 patients with cervical trauma in the experimental group were observed by using Td T- mediated d UTP Nick End Labeling( TUNEL) of DNA fragments and immunohistochemical method. Results In the nucleuspulposustissue,therateofTUNEL-positivecellswas(10.21±1.13)%)intheexperimentalgroupanditwashigherthan(6.34±1.65)%inthecontrolgroup(P0. 01). The rates of Caspase- 1 and IL^-1β proteins- positive cells were( 42. 31 ± 8. 08) % and( 56. 07 ±10. 22) % in the experimental group and they were higher than( 22. 06 ± 1. 28) % and( 43. 12 ± 13. 56) % in the control group( P〈0. 01). Pearson correlation analysis in experimental group showed disc nucleus pulposus TUNEL positive cells and Caspase- 1,IL^-1β- positive cells was positively correlated( the correlation coefficient r = 0. 828 and 0. 780,P〈0. 01). Conclusion In degenerated human intervertebral disc cartilage endplate and nucleus pulposus tissue,highly expressed Caspase- 1 and IL^-1β are involved in the regulation of apoptosis,and this is the cause of discogenic cervical disc degeneration.
出处
《宁夏医科大学学报》
2015年第3期245-247,256,I0002,共5页
Journal of Ningxia Medical University
基金
宁夏医科大学博士点开放课题