Guo Wan-shou, Ma Li, Li Zi-rong
Department of Orthopedics, China-Japan Friendship Hospital, Beijing 100029, China.
Zhonghua Yi Xue Za Zhi. 2004 May 17;84(10):853-6.
To explore the role of interleukin-1 receptor antagonist (IL-1Ra) in suppression of cartilage matrix degradation and pathologic changes.
Thirty New Zealand White rabbits underwent partial synovectomy of the left knee. Synovial fibroblasts were isolated and cultured. The rabbits underwent anterior cruciate ligament transection (ACLT) in the right knee. After the ACLT the rabbits were forced to run 4 hours a day for 4 weeks so as to establish the osteoarthritis (OA) model. Three days after the ACLT the rabbits were randomly divided into 3 groups of 10 rabbits: group 1, to be injected with the cultured autologous synovial fibroblasts into the right knees; group 2, injected with the autologous synovial fibroblasts transfected with marker gene, and group 3, injected with autologous synovial fibroblasts transfected with IL-1Ra gene. Two and 4 weeks after the injection 5 rabbits in each group were killed respectively. Their right knee joints were lavaged and the lavage fluid was extracted. IL-1Ra level in the synovial fluid (SF) was determined by ELISA. 20 mg of articular cartilage were taken from the condyle of right femur and digested by papain. The glycosamino-glycan (GAG) level in the SF and in the cartilage digest were evaluated using dimethylmethylene blue assay. Two pieces of cartilage were taken from each rabbit's and were sliced and stained to undergo pathologic changes.
The IL-1Ra level in the SF of the group 3 was (20.2 +/- 1.8) ng/ml 2 weeks after, and was (4.8 +/- 0.5) ng/ml 4 weeks after, significantly lower than those in the group 2 (84 +/- 7) micro g/ml and group 3 (84 +/- 6) micro g/ml IL-1Ra was not detected in the SF of the group 1. The GAG level in SF was 40.1 micro g/ml with an inhibitory rate of 56.2%, and those in the group 2 and group 3 were 30.2 micro g/mg and 10.8 micro g/mg respectively. The GAG levels 4 weeks after in the cartilage digest of the group 1 and group 2 were (10.1 +/- 1.2) micro g/mg and (10.8 +/- 0.9) micro g/mg respectively, both significantly lower than that in the group 3 [(30 +/- 3) micro g/mg, both P < 0.05]. Pathological examination showed that the articular cartilage of the left knee was all normal in all the rabbits. However, obvious damage was found in the articular cartilage of the right knees of all the rabbits. However, the damage in the group 3 was significantly milder than that in the other 2 groups.
Intraartilcular injection of synovial cells transfected with IL-1Ra gene can suppress articular cartilage matrix degradation and pathologic changes.
探讨白细胞介素-1受体拮抗剂(IL-1Ra)在抑制软骨基质降解及病理改变中的作用。
30只新西兰白兔接受左膝部分滑膜切除术。分离并培养滑膜成纤维细胞。白兔右膝行前交叉韧带切断术(ACLT)。ACLT术后,让白兔每天强迫跑步4小时,持续4周以建立骨关节炎(OA)模型。ACLT术后3天,将白兔随机分为3组,每组10只:第1组,向右膝注射培养的自体滑膜成纤维细胞;第2组,注射转染了标记基因的自体滑膜成纤维细胞;第3组,注射转染了IL-1Ra基因的自体滑膜成纤维细胞。注射后2周和4周,分别处死每组中的5只兔子。冲洗其右膝关节并提取冲洗液。采用酶联免疫吸附测定法(ELISA)测定滑液(SF)中IL-1Ra水平。从右股骨髁取20mg关节软骨,用木瓜蛋白酶消化。采用二甲基亚甲基蓝法评估SF和软骨消化液中糖胺聚糖(GAG)水平。从每只兔子身上取两片软骨,切片并染色以观察病理变化。
第3组注射后2周时SF中IL-1Ra水平为(20.2±1.8)ng/ml,4周时为(4.8±0.5)ng/ml,明显低于第2组(84±7)μg/ml和第3组(84±6)μg/ml。第1组SF中未检测到IL-1Ra。第1组SF中GAG水平为40.1μg/ml,抑制率为56.2%,第2组和第3组分别为30.2μg/mg和10.8μg/mg。第1组和第2组软骨消化液4周后的GAG水平分别为(10.1±1.2)μg/mg和(10.8±0.9)μg/mg,均显著低于第3组[(30±3)μg/mg,P均<0.05]。病理检查显示,所有兔子左膝的关节软骨均正常。然而,所有兔子右膝的关节软骨均发现明显损伤。但第3组的损伤明显轻于其他两组。
关节腔内注射转染IL-1Ra基因的滑膜细胞可抑制关节软骨基质降解及病理改变。