[1]廖太阳 王培民 徐波 张力 李晓辰吴鹏 邢润麟 黄正泉 张农山△.机械敏感性通道蛋白对膝骨关节炎滑膜巨噬细胞焦亡的调控效应分析[J].中国中医骨伤科杂志,2021,29(08):12-17.
 LIAO Taiyang WANG Peimin XU Bo ZHANG Li LI XiaochenWU Peng XIN Runlin HUANG Zhengquan ZHANG Nongshan.Study of the Regulatory Efficacy of Mechanical-Sensitive ChannelProtein(Piezo1)on Cell Pyrolysis in Knee Osteoarthritis[J].Chinese Journal of Traditional Medical Traumatology & Orthopedics,2021,29(08):12-17.
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机械敏感性通道蛋白对膝骨关节炎滑膜巨噬细胞焦亡的调控效应分析()
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《中国中医骨伤科杂志》[ISSN:1005-0205/CN:42-1340/R]

卷:
第29卷
期数:
2021年08期
页码:
12-17
栏目:
实验研究
出版日期:
2021-08-15

文章信息/Info

Title:
Study of the Regulatory Efficacy of Mechanical-Sensitive ChannelProtein(Piezo1)on Cell Pyrolysis in Knee Osteoarthritis
文章编号:
1005-0205(2021)08-0012-06
作者:
廖太阳12 王培民12 徐波12 张力12 李晓辰12吴鹏12 邢润麟12 黄正泉12 张农山12△
1南京中医药大学附属医院(南京,210029)2江苏省中医院
Author(s):
LIAO Taiyang12 WANG Peimin12 XU Bo12 ZHANG Li12 LI Xiaochen12WU Peng12 XIN Runlin12 HUANG Zhengquan12 ZHANG Nongshan12△
1Affiliated Hospital of Nanjing University of Chinese Medicine,Nanjing 210029,China; 2Jiangsu Province Hospital of Chinese Medicine,Nanjing 210029,China.
关键词:
异常机械应力 机械敏感性通道蛋白 膝骨关节炎 滑膜巨噬细胞焦亡
Keywords:
abnormal mechanical stress mechanical-sensitive channel protein knee osteoarthritis pyrolysis of synovial macrophages
分类号:
R-33
文献标志码:
A
摘要:
目的:探讨机械敏感性通道蛋白Piezo1对膝骨关节炎细胞焦亡的调控效应。方法:选取5只SPF 级雄性SD大鼠,提取腹腔巨噬细胞,分为空白对照组、应力拉伸组及应力拉伸+Piezo1抑制剂组。使用FX-5000T细胞牵张拉伸应力加载系统以6个循环/min的周期性频率对BioFlex板内巨噬细胞进行表面干预。Western Blot检测Caspase-1,Caspase-1 p10,GSDMD蛋白表达; 酶联免疫吸附测定(ELISA)检测细胞上清IL-1β及IL-18含量; Hoechst33342/PI细胞双染免疫荧光检测巨噬细胞膜的完整性; 乳酸脱氢酶(LDH)试剂盒检测巨噬细胞培养上清乳酸脱氢酶含量; 荧光倒置显微镜观察线粒体活性氧(ROS)荧光强度。结果:应力拉伸组Caspase-1,Caspase-1 p10及GSDMD蛋白表达水平较空白对照组增加(P<0.05),而应力拉伸+Piezo1抑制剂组较应力拉伸组有所降低,差异有统计学意义(P<0.05); 此外,应力拉伸组较空白对照组培养上清中IL-1β和IL-18含量显著上升,差异有统计学意义(P<0.05),应力拉伸+Piezo1抑制剂组较应力拉伸组含量显著下降,差异有统计学意义(P<0.05); Ho/PI双染发现应力拉伸组细胞膜遭到破坏,碘化丙啶(PI)染色呈现红色荧光,应力拉伸+Piezo1抑制剂组细胞膜较为完整,PI不能染色或者染色较少; 同时,应力拉伸组上清液中LDH含量显著上升,差异有统计学意义(P<0.05); 应力拉伸+抑制剂LDH含量较应力拉伸组则显著下降,差异有统计学意义(P<0.05); 最后ROS荧光检测发现应力拉伸组产生大量红色荧光,而应力拉伸+抑制剂组荧光强度较低。结论:异常机械应力可通过Piezo1离子通道,加剧滑膜巨噬细胞焦亡及推动膝骨关节炎的进程。
Abstract:
To explore the regulatory efficacy of mechanical-sensitive channel protein(Piezo1)on cell pyrolysis in knee osteoarthritis(KOA).Methods:5 SPF male SD rats were selected,and macrophages were extracted and divided into blank control group,stress stretching group and stress stretching + inhibitor group.FX-5000T-intermittent cyclic mechanical tension(FX-5000T-ICMT)was used to perform surface elongation of synovial macrophages in the BioFlex plate at a periodic frequency of 6 cycles/min.Protein expression of Caspase-1,Caspase-1 p10 and GSDMD were detected by Western Blot.Enzyme-linked immunosorbent assay(ELISA)was used to detect the content of IL-1β and IL-18 in cell supernatant.The integrity of macrophage membrane was detected by Hoechst33342/PI cell double-staining immunofluorescence.The content of lactate dehydrogenase(LDH)in the supernatant of macrophage culture was detected by LDH kit.Fluorescence inverted microscope was used to observe the fluorescence intensity of reactive oxygen species(ROS).Results:The protein expression levels of Caspase-1,Caspase-1 p10 and GSDMD in the stress stretching group were increased compared with the blank control group(P<0.05),while that in the stress stretching group + inhibitor group were decreased compared with the stress stretching group(P<0.05).In addition,the content of IL-1β and IL-18 in the supernatant of the stress stretching group was significantly increased compared to the blank control group(P<0.05),while the content of IL-1β and IL-18 in the stress stretching + inhibitor group was significantly decreased compared to the stress stretching group(P<0.05).Ho/PI double staining revealed that the cell membrane of the stress stretching group was damaged,and PI staining showed red fluorescence,while the cell membrane of stress stretching + inhibitor group was more complete,and PI could not be stained or stained less.At the same time,the LDH content in the supernatant of the stress stretching group was significantly increased(P<0.05).LDH content of stress stretching + inhibitor was significantly decreased compared to the stress stretching group(P<0.05).At last,ROS fluorescence detection showed that the stress stretching group produced a large amount of red fluorescence,while the intensity of stress stretching + inhibitor group fluorescence was lower.Conclusion:Abnormal mechanical stress can increase the pyrolysis of synovial macrophages and promote the process of knee osteoarthritis through the Piezo1 ion channel.

参考文献/References:

[1] BANNURU R R,OSANI M C,VAYSBROT E E,et al.OARSI guidelines for the non-surgical management of knee,hip,and polyarticular osteoarthritis[J].Osteoarthritis and Cartilage,2019,27(11):1578-1589.
[2] HAFNER-BRATKOVIC I,PELEGRIN P.Ion homeostasis and ion channels in NLRP3 inflammasome activation and regulation[J].Curr Opin Immunol,2018,52:8-17.
[3] 宋朋飞,蒋诗超,程艳彬,等.Piezo机械敏感性离子通道研究进展[J].中华中医药杂志,2017,32(4):1669-1673.
[4] ZHANG H,LIN C,ZENG C,et al.Synovial macrophage M1 polarisation exacerbates experimental osteoarthritis partially through R-spondin-2[J].Ann Rheum Dis,2018,77(10):1524-1534.
[5] 中华中医药学会骨伤科分会膝痹病(膝骨关节炎)临床诊疗指南制定工作组.中医骨伤科临床诊疗指南·膝痹病(膝骨关节炎)[J].康复学报,2019,29(3):1-7.
[6] 王冰.黄帝内经·素问[M].北京:人民卫生出版社,1956.
[7] 殷涛,邵进,张岩,等.机械敏感性离子通道蛋白Piezo1在椎间盘髓核细胞中的表达及意义[J].中国医药导报,2019,16(12):77-80.
[8] LEE W,LEDDY H A,CHEN Y,et al.Synergy between piezo1 and piezo2 channels confers high-strain mechanosensitivity to articular cartilage[J].Proc Natl Acad Sci USA,2014,111(47):E5114-E5122.
[9] BROZ P,DIXIT V M.Inflammasomes:mechanism of assembly,regulation and signalling[J].Nat Rev Immunol,2016,16(7):407-420.
[10] ZHANG L,XING R,HUANG Z,et al.Inhibition of synovial macrophage pyroptosis alleviates synovitis and fibrosis in knee osteoarthritis[J].Mediators Inflamm,2019:2165918.
[11] ZHANG L,XING R,HUANG Z,et al.Piezo1 and piezo2 are essential components of distinct mechanically activated cation channels[J].Science,2010,330(6000):55-60.
[12] COSTE B,XIAO B,SANTOS J S,et al.Piezo proteins are pore-forming subunits of mechanically activated channels[J].Nature,2012,483(7388):176-181.
[13] ZHAO C,SUN Q,TANG L,et al.Mechanosensitive ion channel piezo1 regulates diet-induced adipose inflammation and systemic insulin resistance[J].Front Endocrinol(Lausanne),2019,10:373.
[14] ALBARRAN-JUAREZ J,IRING A,WANG S,et al.Piezo1 and Gq/G11 promote endothelial inflammation depending on flow pattern and integrin activation[J].J Exp Med,2018,215(10):2655-2672.
[15] SHI J,GAO W,SHAO F.Pyroptosis:gasdermin-mediated programmed necrotic cell death[J].Trends Biochem Sci,2017,42(4):245-254.
[16] SHI J,ZHAO Y,WANG K,et al.Cleavage of GSDMD by inflammatory caspases determines pyroptotic cell death[J].Nature,2015,526(7575):660-665.
[17] YUAN J,NAJAFOV A,PY B F.Roles of caspases in necrotic cell death[J].Cell,2016,167(7):1693-1704.
[18] SUN Y,LENG P,SONG M,et al.Piezo1 activates the NLRP3 inflammasome in nucleus pulposus cell-mediated by Ca2+/NF-κB pathway[J].Int Immunopharmacol,2020,85:106681.
[19] 何琪,张罡瑜,王海彬,等.大型跨膜蛋白Piezo1在骨科相关疾病中的参与及意义[J].中国组织工程研究,2020,24(30):4882-4888.
[20] HANNEMANN N,CAO S,ERIKSSON D,et al.Transcription factor Fra-1 targets arginase-1 to enhance macrophage-mediated inflammation in arthritis[J].J Clin Invest,2019,129(7):2669-2684.
[21] CHOI S,YOU S,KIM D,et al.Transcription factor NFAT5 promotes macrophage survival in rheumatoid arthritis[J].J Clin Invest,2017,127(3):954-969.
[22] LI X F,ZHANG Z,CHEN Z K,et al.Piezo1 protein induces the apoptosis of human osteoarthritis-derived chondrocytes by activating caspase-12,the signaling marker of ER stress[J].Int J Mol Med,2017,40(3):845-853.

备注/Memo

备注/Memo:
基金项目:江苏省自然科学基金项目(BK20171513)江苏省第十六批“六大人才高峰”高层次人才项目(WSW-014)
通信作者 E-mail:zns0032@163.com
更新日期/Last Update: 2021-08-15