首页> 外文期刊>International journal of molecular medicine >Aquaporin 1 contributes to chondrocyte apoptosis in a rat model of osteoarthritis
【24h】

Aquaporin 1 contributes to chondrocyte apoptosis in a rat model of osteoarthritis

机译:水通道蛋白1在骨关节炎大鼠模型中促进软骨细胞凋亡

获取原文
获取原文并翻译 | 示例
       

摘要

Aquaporins (AQPs) have been found to be associated with a number of diseases. However, the role of AQP-1 in the pathogenesis of osteoarthritis remains unclear. We previously found that AQP-1 expression was upregulated in osteoarthritic cartilage and strongly correlated with caspase-3 expression and activity. The aim of this study was to further investigate the association of AQP-1 expression with chondrocyte apoptosis in a rat model of osteoarthritis, using RNA interference to knock down AQP-1. For this purspose, 72 male Sprague-Dawley rats were randomly assigned to 3 groups as follows: the control group not treated surgically (n=24), the sham-operated group (n=24), and the osteoarthritis group (n=24). Osteoarthritis was induced by amputating the anterior cruciate ligament and medial collateral ligament and partially excising the medial meniscus. Chondrocytes from the rats with osteoarthritis were isolated and cultured. shRNAs were used to knock down AQP-1 expression in the cultured chondrocytes. The expression of AQP-1 and caspase-3 was determined by reverse transcription quantitative polymerase chain reaction. Caspase-3 activity was measured using a caspase-3 colorimetric assay. The rats in our model of osteoarthritis exhibited severe cartilage damage. The knockdown of AQP-1 decreased caspase-3 expression and activity in the cultured chondrocytes. In addition, the expression of AQP-1 positively correlated with caspase-3 expression and activity. Thus, the findings of our study, suggest that AQP-1 promotes caspase-3 activation and thereby contributes to chondrocyte apoptosis and to the development of osteoarthritis.
机译:已经发现水通道蛋白(AQP)与许多疾病有关。然而,AQP-1在骨关节炎发病机理中的作用尚不清楚。我们先前发现,AQP-1表达在骨关节炎软骨中上调,并且与caspase-3表达和活性密切相关。这项研究的目的是使用RNA干扰敲低AQP-1,进一步研究AQP-1表达与骨关节炎大鼠软骨细胞凋亡的关系。为此,将72只雄性Sprague-Dawley大鼠随机分为3组:未手术治疗的对照组(n = 24),假手术组(n = 24)和骨关节炎组(n = 24 )。骨关节炎是通过切除前交叉韧带和内侧副韧带并部分切除内侧半月板而诱发的。分离并培养来自患有骨关节炎的大鼠的软骨细胞。 shRNA被用于敲除培养的软骨细胞中AQP-1的表达。通过反转录定量聚合酶链反应确定AQP-1和caspase-3的表达。使用胱天蛋白酶3比色测定法测量胱天蛋白酶3活性。在我们的骨关节炎模型中,大鼠表现出严重的软骨损伤。敲低AQP-1会降低培养的软骨细胞中caspase-3的表达和活性。此外,AQP-1的表达与caspase-3的表达和活性呈正相关。因此,我们研究的结果表明,AQP-1促进caspase-3活化,从而促进软骨细胞凋亡和骨关节炎的发展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号