Aslan Joseph E, Itakura Asako, Gertz Jacqueline M, McCarty Owen J T
Department of Biomedical Engineering, Department of Cell and Developmental Biology, Oregon Health & Science University, Portland, OR, USA.
Methods Mol Biol. 2012;788:91-100. doi: 10.1007/978-1-61779-307-3_7.
Hemostasis is dependent upon the successful recruitment and activation of blood platelets to the site of a breach in the vasculature. Platelet activation stimulates the rapid reorganization of the cortical actin cytoskeleton, resulting in the transformation of platelets from biconcave disks to fully spread cells. During this process, platelets extend filopodia and generate lamellipodia, resulting in a dramatic increase in the platelet surface area. Kohler-illuminated Nomarski Differential Interference Contrast microscopy has proved an effective tool to characterize platelet morphological changes in real time, and provides a useful tool to identify genetic and pharmacological regulators of platelet function.
止血依赖于血管破裂部位成功募集和激活血小板。血小板激活刺激皮质肌动蛋白细胞骨架快速重组,导致血小板从双凹圆盘转变为完全铺展的细胞。在此过程中,血小板伸出丝状伪足并形成片状伪足,导致血小板表面积急剧增加。柯勒照明的诺马斯基微分干涉对比显微镜已被证明是实时表征血小板形态变化的有效工具,并为鉴定血小板功能的遗传和药理学调节剂提供了有用的工具。