中华血液学杂志
中華血液學雜誌
중화혈액학잡지
Chinese Journal of Hematology
2010年
3期
176-180
,共5页
高广勋%董红娟%顾宏涛%高瑛%潘耀柱%王一苇%杨阳%陈协群
高廣勛%董紅娟%顧宏濤%高瑛%潘耀柱%王一葦%楊暘%陳協群
고엄훈%동홍연%고굉도%고영%반요주%왕일위%양양%진협군
哺乳类,diaphanous%磷脂酰肌醇3激酶%血小板%凝血酶
哺乳類,diaphanous%燐脂酰肌醇3激酶%血小闆%凝血酶
포유류,diaphanous%린지선기순3격매%혈소판%응혈매
mDial%PI3K%Platelets%Thrombi
目的 探讨mDial(mammalian diaphanous 1)在人血小板中的表达和血小板聚集过程中的作用以及磷脂酰肌醇3激酶(PI3K)对该过程的调控作用.方法 采用血小板聚集仪检测PI3K抑制剂和抗mDial抗体导入后对人血小板聚集率的影响;Western blot法检测mDial在血小板静止及活化过程中的表达及其与肌动蛋白细胞骨架的关系.结果 mDial在血小板静止、凝血酶诱导的铺展或聚集血小板内表达水平没有明显差异;凝血酶诱导血小板聚集过程中,mDial从Triton-X100可溶性(胞质)部分向Triton-X100不可溶性(细胞骨架)部分转位;抗mDial抗体导入血小板后能够抑制凝血酶诱导的血小板聚集;PI3K抑制剂渥曼青霉素及Ly294002能够抑制血小板聚集,抑制mDial从Triton-X100可溶性部分向Triton-X100不可溶性部分的转位.结论 PI3K通过mDial参与调控凝血酶诱导的血小板聚集过程中肌动蛋白细胞骨架的重构.
目的 探討mDial(mammalian diaphanous 1)在人血小闆中的錶達和血小闆聚集過程中的作用以及燐脂酰肌醇3激酶(PI3K)對該過程的調控作用.方法 採用血小闆聚集儀檢測PI3K抑製劑和抗mDial抗體導入後對人血小闆聚集率的影響;Western blot法檢測mDial在血小闆靜止及活化過程中的錶達及其與肌動蛋白細胞骨架的關繫.結果 mDial在血小闆靜止、凝血酶誘導的鋪展或聚集血小闆內錶達水平沒有明顯差異;凝血酶誘導血小闆聚集過程中,mDial從Triton-X100可溶性(胞質)部分嚮Triton-X100不可溶性(細胞骨架)部分轉位;抗mDial抗體導入血小闆後能夠抑製凝血酶誘導的血小闆聚集;PI3K抑製劑渥曼青黴素及Ly294002能夠抑製血小闆聚集,抑製mDial從Triton-X100可溶性部分嚮Triton-X100不可溶性部分的轉位.結論 PI3K通過mDial參與調控凝血酶誘導的血小闆聚集過程中肌動蛋白細胞骨架的重構.
목적 탐토mDial(mammalian diaphanous 1)재인혈소판중적표체화혈소판취집과정중적작용이급린지선기순3격매(PI3K)대해과정적조공작용.방법 채용혈소판취집의검측PI3K억제제화항mDial항체도입후대인혈소판취집솔적영향;Western blot법검측mDial재혈소판정지급활화과정중적표체급기여기동단백세포골가적관계.결과 mDial재혈소판정지、응혈매유도적포전혹취집혈소판내표체수평몰유명현차이;응혈매유도혈소판취집과정중,mDial종Triton-X100가용성(포질)부분향Triton-X100불가용성(세포골가)부분전위;항mDial항체도입혈소판후능구억제응혈매유도적혈소판취집;PI3K억제제악만청매소급Ly294002능구억제혈소판취집,억제mDial종Triton-X100가용성부분향Triton-X100불가용성부분적전위.결론 PI3K통과mDial삼여조공응혈매유도적혈소판취집과정중기동단백세포골가적중구.
Objective To investigate the expression of mDial(mammalian diaphanous 1)in platelet and the role of mDial or phosphatidylinositol 3-kinase(PI3K)in the process of thrombin-induced platelet aggregation.Methods The extent of platelet aggregation was measured by a platelet aggregation system and the expression of mDial and its relation with F-actin in quiescent,spreading or aggregated platelets by Western blot.Results There was no significant difference in mDial expression level between quiescent and activated platelets.mDial moved from a Triton-X100-soluble cytosolie fraction to insoluble eytoskeleton fraction after thrombin induced platelets aggregation.Anti-mDial antibody could inhibit this aggregation.PI3K inhibitor Wortmannin or Ly294002 inhibited the thrombin induced platelet aggregation and the above mentioned mDial translocation.Conclusion PI3-kinase mediates the thrombin-induced platelet aggregation through mDial pathway.