双孔钾通道task-1在缺氧性肺血管收缩中的作用及机制分析-role and mechanism of double-hole potassium channel task - 1 in hypoxic pulmonary vasoconstriction.docxVIP
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双孔钾通道task-1在缺氧性肺血管收缩中的作用及机制分析-role and mechanism of double-hole potassium channel task - 1 in hypoxic pulmonary vasoconstriction
双孔钾通道TASK-1在缺氧性肺血管收缩中的作用及机制研究中文摘要目的:1.观察双孔钾通道TASK-1在缺氧所致肺动脉血管环张力改变中的作用。2.探讨双孔钾离子通道TASK-1介导缺氧性肺动脉收缩可能的机制。方法:从胸心外科手术室获得肺肿瘤患者切除的肺组织,然后分离三、四级肺动脉分支,制成肺动脉环,采用RM-6000多导生理记录仪,观察经c-Src抑制剂PP2、PP2类似物PP3、酪氨酸磷酸酯酶抑制剂bpv预处理后,对缺氧所致血管环张力改变的影响及TASK-1抑制剂A-293预孵育(100μM)后PP2对缺氧所致动脉环张力改变的影响。经组织块培养法获取原代培养人肺动脉平滑肌细胞(humanpulmonaryarterysmoothmusclecells,hPASMCs),经间接免疫荧光染色方法鉴定。第3至第6代用于膜片钳实验,观察缺氧、A-293、PP2、PP3、bpv预处理后对TASK-1电流的影响。结果:1.在适宜前负荷下,肺动脉应用TASK-1抑制剂A-293后,A-293抑制肺动脉缺氧性收缩反应,血管张力从1382±263mg降至1138±219mg,p0.05。2.在适宜前负荷下,肺动脉应用c-Src抑制剂PP2、PP3、bpv后,c-Src抑制剂PP2抑制肺动脉缺氧性收缩反应,血管张力分从1379±231mg降至1103±215mg,p0.05;PP3对肺动脉缺氧性收缩反应无影响,血管张力从1403±203mg降至1381±198mg,P0.05;酪氨酸磷酸酯酶抑制剂bpV增强肺动脉缺氧性收缩反应,血管张力从1351±213mg升至1632±253mg,p0.05。3.在适宜前负荷下,肺动脉应用A-293预孵育后加入PP2,PP2对肺动脉缺氧性收缩反应无影响,血管环张力1412±264mg至1356±243mg,P0.05。4.缺氧可逆性明显抑制肺动脉平滑肌细胞TASK-1电流(电流密度从0.57±0.06pA/pF至0.27±0.04pA/pF,p0.01),而TASK-1抑制剂A-293可阻断该抑制效应。5.c-Src特异性抑制剂PP2预处理后,肺动脉平滑肌细胞缺氧敏感性TASK-1电流消失(电流密度从0.28±0.04pA/pF至0.26±0.05pA/pF,P0.05);但是PP2类似物PP3预处理后,缺氧仍然可逆性抑制肺动脉平滑肌细胞TASK-1(电流密度从0.58±0.04pA/pF至0.25±0.06pA/pF,p0.01)。此外,酪氨酸磷酸酯酶抑制剂bpv预处理后,肺动脉平滑肌细胞TASK-1电流明显增加(电流密度从0.57±0.06pA/pF至0.74±0.07pA/pF,p0.01),缺氧可明显抑制该电流(电流密度从0.74±0.07pA/pF至0.26±0.05pA/pF,p0.01)结论:1.双孔钾通道TASK-1参与人肺血管缺氧性收缩反应。2.双孔钾通道TASK-1介导人肺血管缺氧性收缩反应的过程具c-Src依赖性。3.缺氧可逆性抑制肺动脉平滑肌细胞TASK-1电流。4.酪氨酸激酶c-Src可调控双孔钾通道TASK-1。5.双孔钾通道TASK-1对人肺血管缺氧性收缩反应是通过c-Src对钾通道TASK-1的调控来实现的。关键词:肺动脉高压、双孔钾通道TASK-1、c-Src、缺氧性肺血管收缩。Purpose:Toinvestigatetheexactroleofthetwo-poredomainpotassiumchannelTASK-1inthetensionchangeofpulmonaryvascularringcausedbyhypoxia.Toinvestigatethemechanismofthetwo-poredomainpotassiumchannelTASK-1inducedpulmonaryvasoconstrictioncausedbyhypoxia.Methods:Resectedlungtissueswereobtainedfromlungcancerpatientswhounderwentsurgeryandthenthethirdorfourthbranchesofthepulmonaryarterieswereseparatedtomakepulmonaryarteryrings.RM-6000multi-channelpolygraphwasusedtoobservetheimpactonthetensionofvascularringswhichwerepre-incubatedwithc-SrcinhibitorPP2,PP2-likePP3,tyrosinephosphataseinhibitorbpvandTASK-1inhibitora-293(
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