中国病理生理杂志
中國病理生理雜誌
중국병리생리잡지
CHINESE JOURNAL OF PATHOPHYSIOLOGY
2014年
6期
1039-1046
,共8页
林洪升%杨海波%谢恺庆%杨利%周静文%周马林%黄企光
林洪升%楊海波%謝愷慶%楊利%週靜文%週馬林%黃企光
림홍승%양해파%사개경%양리%주정문%주마림%황기광
Toll样受体类%肾小管上皮细胞%牛型结核分枝杆菌
Toll樣受體類%腎小管上皮細胞%牛型結覈分枝桿菌
Toll양수체류%신소관상피세포%우형결핵분지간균
Toll-like receptors%Renal tubule epithelial cells%Mycobacterium bovis
目的:探讨Toll样受体(TLR)2和TLR4在牛型结核分枝杆菌卡介苗(BCG)诱导的人肾小管上皮细胞( HK-2细胞)损伤中的作用。方法:用BCG刺激HK-2细胞,通过荧光定量PCR和Western blotting 方法分别检测TLR2、TLR4、转化生长因子β1( TGF-β1)和趋化因子CX3CL1的表达。将TLR2抗体和TLR4拮抗剂CLI-90分别与BCG共刺激HK-2细胞,通过荧光定量PCR和Western blotting方法分别检测TGF-β1和CX3CL1的表达水平。结果:BCG刺激HK-2细胞可诱导TLR2、TLR4、TGF-β1和CX3CL1表达上调,TLR2抗体和TLR4拮抗剂可部分抑制BCG引起的TGF-β1和CX3CL1表达上调。结论:BCG可通过激活TLR2和TLR4引起TGF-β1和CX3CL1表达上调,提示TLR2和TLR4介导的信号通路在结核分枝杆菌致肾小管上皮细胞损伤中发挥重要作用。
目的:探討Toll樣受體(TLR)2和TLR4在牛型結覈分枝桿菌卡介苗(BCG)誘導的人腎小管上皮細胞( HK-2細胞)損傷中的作用。方法:用BCG刺激HK-2細胞,通過熒光定量PCR和Western blotting 方法分彆檢測TLR2、TLR4、轉化生長因子β1( TGF-β1)和趨化因子CX3CL1的錶達。將TLR2抗體和TLR4拮抗劑CLI-90分彆與BCG共刺激HK-2細胞,通過熒光定量PCR和Western blotting方法分彆檢測TGF-β1和CX3CL1的錶達水平。結果:BCG刺激HK-2細胞可誘導TLR2、TLR4、TGF-β1和CX3CL1錶達上調,TLR2抗體和TLR4拮抗劑可部分抑製BCG引起的TGF-β1和CX3CL1錶達上調。結論:BCG可通過激活TLR2和TLR4引起TGF-β1和CX3CL1錶達上調,提示TLR2和TLR4介導的信號通路在結覈分枝桿菌緻腎小管上皮細胞損傷中髮揮重要作用。
목적:탐토Toll양수체(TLR)2화TLR4재우형결핵분지간균잡개묘(BCG)유도적인신소관상피세포( HK-2세포)손상중적작용。방법:용BCG자격HK-2세포,통과형광정량PCR화Western blotting 방법분별검측TLR2、TLR4、전화생장인자β1( TGF-β1)화추화인자CX3CL1적표체。장TLR2항체화TLR4길항제CLI-90분별여BCG공자격HK-2세포,통과형광정량PCR화Western blotting방법분별검측TGF-β1화CX3CL1적표체수평。결과:BCG자격HK-2세포가유도TLR2、TLR4、TGF-β1화CX3CL1표체상조,TLR2항체화TLR4길항제가부분억제BCG인기적TGF-β1화CX3CL1표체상조。결론:BCG가통과격활TLR2화TLR4인기TGF-β1화CX3CL1표체상조,제시TLR2화TLR4개도적신호통로재결핵분지간균치신소관상피세포손상중발휘중요작용。
AIM:To explore the effect of Toll-like receptor ( TLR) 2 and TLR4 in Mycobacterium bovis Bacil-lus Calmette-Guérin (BCG)-induced human proximal renal tubule epithelial cell (HK-2) injury.METHODS:HK-2 cells were stimulated by BCG, and the expression of TLR2, TLR4, chemokine (C-X3-C motif) ligand 1 (CX3CL1) and trans-forming growth factor beta 1 ( TGF-β1 ) was detected by quantitative real-time PCR and Western blotting .TLR2 monoclonal antibody and TLR4 inhibitor were used to treat the HK-2 cells 1 h before BCG stimulation.The expression of CX3CL1 and TGF-β1 was evaluated by quantitative real-time PCR and Western blotting .RESULTS: BCG increased the expression of TLR2, TLR4, CX3CL1 and TGF-β1 in the HK-2 cells.Additionally, the expression of CX3CL1 and TGF-β1 was inhibited partly by TLR2 monoclonal antibody or TLR4 inhibitor.CONCLUSION:BCG is able to increase the production of TLR 2, TLR4, CX3CL1 and TGF-β1 in the HK-2 cells.TLR2 and TLR4 signaling pathways play important roles in tubule epitheli-al cell injury induced by BCG .