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[利用跳跃探针离子电导显微镜实时研究活血小板的动态形态及血小板微粒的生成]

[Real-time investigation of dynamic morphology of live platelets and generation of platelet microparticles using hopping probe ion conductance microscopy].

作者信息

Liu Xiao, Luo Yufu, Zhang Yanjun

机构信息

China National Academy of Nanotechnology & Engineering, Tianjin 300457, P.R.China.

Tianjin Yongjiu Hospital, Tianjin 300450, P.R.China.

出版信息

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2017 Aug 1;34(5):767-771. doi: 10.7507/1001-5515.201611004.

DOI:10.7507/1001-5515.201611004
PMID:29761964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9935462/
Abstract

Platelets are rapidly activated by activators and produce a large number of platelet microparticles (PMPs) with high coagulation activity, resulting in coagulation dysfunction. However, the generation mechanism of PMPs is still not clear. Hopping probe ion conductance microscopy (HPICM) has special technical advantages in non-contact, real-time, high-resolution imaging of living cells under physiological conditions. Using HPICM, this study monitored the processes of platelet activation and generation of PMPs in real time in the presence of calcium ionophore A23187 and cytochalasin D (CD), respectively. The results proved that the intracellular calcium concentration and the cytoskeletal proteins played important roles in the platelet activation and the generation of PMPs. Compared with the low density spread shape platelets (LDSS), the high density bubble shape platelets (HDBS) were more sensitive to the calcium ionophore A23187 and cytochalasin D. This research has a guiding significance for the further study on the relationship between platelet activation and coagulation function using HPICM.

摘要

血小板被激活剂迅速激活,并产生大量具有高凝血活性的血小板微粒(PMPs),导致凝血功能障碍。然而,PMPs的产生机制仍不清楚。跳跃探针离子电导显微镜(HPICM)在生理条件下对活细胞进行非接触、实时、高分辨率成像方面具有特殊的技术优势。本研究利用HPICM分别在钙离子载体A23187和细胞松弛素D(CD)存在的情况下实时监测血小板激活和PMPs产生的过程。结果证明,细胞内钙浓度和细胞骨架蛋白在血小板激活和PMPs产生中起重要作用。与低密度铺展形血小板(LDSS)相比,高密度泡状血小板(HDBS)对钙离子载体A23187和细胞松弛素D更敏感。本研究对利用HPICM进一步研究血小板激活与凝血功能之间的关系具有指导意义。

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本文引用的文献

1
Use of non-contact hopping probe ion conductance microscopy to investigate dynamic morphology of live platelets.使用非接触跳跃探针离子电导显微镜研究活血小板的动态形态。
Platelets. 2015;26(5):480-5. doi: 10.3109/09537104.2014.940888. Epub 2014 Aug 7.
2
Contact- and agonist-regulated microvesiculation of human platelets.人血小板的接触和激动剂调节的微泡形成。
Thromb Haemost. 2013 Aug;110(2):331-9. doi: 10.1160/TH12-11-0853. Epub 2013 Jun 20.
3
Real-time investigation of acute toxicity of ZnO nanoparticles on human lung epithelia with hopping probe ion conductance microscopy. hopping 探针离子电导显微镜实时研究 ZnO 纳米颗粒对人肺上皮细胞的急性毒性
Chem Res Toxicol. 2012 Feb 20;25(2):297-304. doi: 10.1021/tx2004823. Epub 2012 Jan 6.
4
High-resolution morphological identification and characterization of living neuroblastoma SK-N-SH cells by hopping probe ion conductance microscopy. hopping 探针离子电导显微镜术对活 SK-N-SH 神经母细胞瘤细胞的高分辨率形态学鉴定和特征描述。
Brain Res. 2011 Apr 22;1386:35-40. doi: 10.1016/j.brainres.2011.02.053. Epub 2011 Feb 24.
5
Platelet-derived microparticles - an updated perspective.血小板衍生的微粒体——一个更新的视角。
Thromb Res. 2011 Jan;127 Suppl 2:S30-3. doi: 10.1016/S0049-3848(10)70152-3.
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Cellular mechanisms underlying the formation of circulating microparticles.循环微颗粒形成的细胞机制。
Arterioscler Thromb Vasc Biol. 2011 Jan;31(1):15-26. doi: 10.1161/ATVBAHA.109.200956.
7
Comparison of scanning ion conductance microscopy with atomic force microscopy for cell imaging.扫描离子电导显微镜与原子力显微镜在细胞成像中的比较。
Langmuir. 2011 Jan 18;27(2):697-704. doi: 10.1021/la103275y. Epub 2010 Dec 15.
8
Microparticle size and its relation to composition, functional activity, and clinical significance.微粒大小及其与组成、功能活性和临床意义的关系。
Semin Thromb Hemost. 2010 Nov;36(8):876-80. doi: 10.1055/s-0030-1267041. Epub 2010 Nov 3.
9
[Change in plasma microparticle procoagulant activity after traumatic brain injury].[创伤性脑损伤后血浆微粒促凝活性的变化]
Zhonghua Yi Xue Za Zhi. 2009 Aug 25;89(32):2265-8.
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A multicolor flow cytometric assay for measurement of platelet-derived microparticles.一种用于测量血小板衍生微粒的多色流式细胞术检测方法。
Thromb Res. 2010 Mar;125(3):e110-6. doi: 10.1016/j.thromres.2009.10.006. Epub 2009 Nov 24.