文章摘要
任莎莎,李雪萍,林强,程凯,夏鹏,杨怀春,高明霞.低强度脉冲超声经PI3K/Akt通路调控兔膝骨性关节炎软骨细胞凋亡的作用机制研究[J].中国康复,2015,30(2):83-87
低强度脉冲超声经PI3K/Akt通路调控兔膝骨性关节炎软骨细胞凋亡的作用机制研究
The action mechanism of low intensity pulsed ultrasound regulating chondrocytes apoptosis in rabbits with osteoarthritis via activating PI3K/Akt pathway
  
DOI:
中文关键词: 低强度脉冲超声  软骨细胞  PI3K/Akt通路  凋亡
英文关键词: ultrasound  chondrocytes  PI3K/Akt pathway  apoptosis
基金项目:国家自然科学基金(81272151)
作者单位
任莎莎 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
李雪萍 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
林强 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
程凯 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
夏鹏 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
杨怀春 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
高明霞 南京医科大学附属南京医院(南京市第一医院)康复医学科南京 210006 
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中文摘要:
  目的:探讨低强度脉冲超声(LIPUS)对兔膝骨性关节炎(OA)软骨细胞凋亡的影响及有关作用机制。方法:共选取30只新西兰大白兔,随机分为正常对照组(A组)、OA模型组(B组)、OA+LIPUS组(C组)、OA+LY294002(PI3K/Akt抑制剂)组(D组)、OA+LY294002+LIPUS组(E组),每组各6只。采用右后膝前交叉韧带切断术(ACLT)造模。于造模后第6周时采用空气栓塞法处死实验兔,切取软骨组织进行组织学观察,并进行Mankin评分;提取软骨细胞进行体外培养并采用免疫组化染色法鉴定;应用western blot检测各组软骨细胞中Ⅱ型胶原(COL2)、MMP-13、Akt、pAkt、P53、Bcl-2蛋白表达情况。结果:B组COL2、pAkt、Bcl-2蛋白含量较A组降低,MMP-13、P53蛋白含量较A组增高(P<0.05)。与B组相比,C组COL2、pAkt、Bc-2蛋白含量增高,MMP-13、P53蛋白含量下降(P<0.05);D组COL2、Bcl-2、pAkt蛋白含量下降,MMP-13、P53蛋白含量升高(P<0.05),E组COL2、MMP-13、P53、Bcl-2、pAkt蛋白含量无明显变化,但与C组、D组相比差异显著(P<0.05)。各组Akt蛋白表达无明显差异。结论:LIPUS能通过PI3K/Akt通路降低兔膝骨性关节炎软骨细胞凋亡率,促进抗凋亡基因Bcl-2表达,下调促凋亡基因P53水平,促进关节软骨损伤修复。
英文摘要:
  Objective: To investigate the effects of low intensity pulsed ultrasound (LIPUS) on the apoptosis of chondrocytes in rabbits with osteoarthritis (OA) and explore the underlying mechanism. Methods: Thirty healthy New Zealand white rabbits were selected for this study. All the cultured cells were randomly divided into five groups: a normal control group (A group), an OA model group (B group), an OA model plus LIPUS group (C group), an OA model plus PI3K/Akt inhibitor group (D group), and an OA model plus PI3K/Akt inhibitor and LIPUS group (E group). The OA model was made by knee anterior cruciate ligament transection. At the 6th week after modeling, the rabbits were sacrificed by air embolism method and pathologic changes were assessed on articular surface of femoral condyles. Meanwhile chondrocytes were isolated and cultured in vitro, and cultured cells were identified by immuohistochemistry. The expression of collagen protein type Ⅱ, MMP-13, Akt, pAkt, P53, and Bcl-2 was detected by Western blotting. Results: As compared with the A group, the expression of collagen type Ⅱ, pAkt and Bcl-2 was significantly reduced in the B group, but that of MMP-13 and P53 was significantly increased in the B group (P<0.05). As compared with the B group, the expression of collagen type Ⅱ, pAkt and Bcl-2 was significantly increased, and that of MMP-13 and P53 was significantly reduced in the C group (P<0.05); the expression of collagen type Ⅱ, pAkt and Bcl-2 was significantly reduced (P<0.05), and that of MMP-13 and P53 was significantly increased in the D group (P<0.05). Although the expression of collagen type Ⅱ, MMP-13, pAkt, P53, and Bcl2 showed no significant difference between the E group and the B group, the expression of collagen type Ⅱ, MMP-13, pAkt, P53 and Bcl-2 showed significant difference between C group and D group (P<0.05). There was no significant difference in the expression of Akt among all groups. Conclusions: The LIPUS can obviously decrease the apoptosis rate of chondrocytes in the knee joints of OA rabbits via activating PI3K/Akt pathway, and the underlying mechanisms are closely related to upregulation of Bcl-2 expression and downregulation of P53 expression. The LIPUS can accelerate the recovery of cartilage for the purpose of treatment of OA.
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