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血小板衍生膜微粒对人脐静脉内皮细胞增殖和凋亡的影响
引用本文:仲悦娇,陈宝安,HUANG Cheng-Yin,LI Cui-Ping,高峰,费菲,裴孝平,高冲,丁家华,孙耘玉,程坚,王骏,赵刚,马燕. 血小板衍生膜微粒对人脐静脉内皮细胞增殖和凋亡的影响[J]. 中国实验血液学杂志, 2007, 15(4): 858-861
作者姓名:仲悦娇  陈宝安  HUANG Cheng-Yin  LI Cui-Ping  高峰  费菲  裴孝平  高冲  丁家华  孙耘玉  程坚  王骏  赵刚  马燕
作者单位:东南大学中大医院血液科,南京,210009
摘    要:
本研究探讨血小板衍生膜微粒(platelet-derived membrane microparticles,PMP)对人脐静脉内皮细胞(hu-man umbilical vein endothelial cells,HUVEC)增殖和凋亡的影响。用不同浓度的凝血酶激活血小板释放出PMP,采用流式细胞术检测PMP的释放量,确定制备PMP时凝血酶的最佳应用浓度。以体外培养HUVEC为载体,通过噻唑蓝(MTT)实验和流式细胞术研究不同浓度的PMP对HUVEC增殖和凋亡的影响。结果表明,2、1.5、1.0和0.5U/ml凝血酶激活血小板后PMP的释放率分别为28.7、47.7、50.1和43.9%;HUVEC的增殖与PMP呈剂量依赖关系。在培养液中添加40μg/mlPMP时,HUVEC增殖是空白对照组的1.8±0.3倍;10μl/ml血管内皮细胞生长因子(VEGF)组的HUVEC增殖是空白对照组的1.9±0.5倍,两组之间无统计学差异,(p〉0.05);PMP能抑制HUVEC的凋亡,40μg/mlPMP组的细胞凋亡率为(3.9±0.4)%,明显低于空白对照组的细胞凋亡率(9.4±0.5)%(p〈0.05)。VEGF(10μl/ml)对HUVEC细胞的凋亡无明显抑制作用,其凋亡率为(8.0±0.8)%。结论:用1U/ml的凝血酶刺激血小板释放的PMP较为均一,且释放量最大,可促进HUVEC细胞的增殖并抑制其凋亡。

关 键 词:血小板衍生膜微粒  人脐静脉内皮细胞  细胞增殖  细胞凋亡
文章编号:1009-2137(2007)04-0858-04
修稿时间:2006-06-12

Effects of Platelet-derived Membrane Microparticles on the Proliferation and Apoptosis of Human Umbilical Vein Endothelial Cells
ZHONG Yue-Jiao,CHEN Bao-An,HUANG Cheng-Yin,LI Cui-Ping,GAO Feng,FEI Fei,PEI Xiao-Ping,GAO Chong,DING Jia-Hua,SUN Yun-Yu,CHENG Jian,WANG Jun,ZHAO Gang,MA Yan. Effects of Platelet-derived Membrane Microparticles on the Proliferation and Apoptosis of Human Umbilical Vein Endothelial Cells[J]. Journal of experimental hematology, 2007, 15(4): 858-861
Authors:ZHONG Yue-Jiao  CHEN Bao-An  HUANG Cheng-Yin  LI Cui-Ping  GAO Feng  FEI Fei  PEI Xiao-Ping  GAO Chong  DING Jia-Hua  SUN Yun-Yu  CHENG Jian  WANG Jun  ZHAO Gang  MA Yan
Affiliation:1.Department of Hematology, Zhongda Hospital , Southeast University, Nanjing 210009, China; 2. Jiangsu Province Blood Center, Nanjing 210042, China
Abstract:
This study was purposed to investigate the effects of platelet-derived membrane microparticles (PMP) on the proliferation and apoptosis of human umbilical vein endothelial cells (HUVEC). Different concentrations of thrombin were adopted to activate the platelets so as to release PMPs. Flow cytometry (FCM) was adopted to evaluate the efficiencies of different concentrations of thrombin to release PMPs. By using the HUVEC cultivated in vitro as vector, the effects of PMPs on the proliferation and apoptosis of HUVEC were investigated by MTT and FCM. The results showed that the efficiencies releasing PMPs from platelets activated by 2.0, 1.5, 1.0, 0.5 U/ml thrombin were 28.7, 47.7, 50.1 and 43.9% respectively; PMPs induced proliferation of HUVEC in a dose dependent manner. At the concentration of 40 microg/ml PMPs, the proliferation rate of HUVEC was 1.8 +/- 0.3 times as much as blank control, the proliferation rate in group of vascular endothelial growth factor was 1.9 +/- 0.5 times of as much as blank control, there was no statistic difference (p > 0.05). The PMPs inhibited HUVEC apoptosis. Compared with the apoptosis rate of control (9.4 +/- 0.5)%, apoptosis rate in PMP group (40 microg/ml) was (3.9 +/- 0.4)% (p < 0.05). The addition of VEGF (10 microl/ml) did not successfully prevented apoptosis of HUVEC with apoptosis rate of (8.0 +/- 0.8)%. It is concluded that platelets activated by 1 U/ml thrombin gets the best efficiency of PMP release, which stimulates proliferation of HUVEC and inhibits its apoptosis.
Keywords:platelet-derived microparticle   human umbilical vein endothelial cell   proliferation   apoptosis
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