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超声激活的充气微孔在体外从人红细胞中释放血红蛋白和抗原。

Ultrasonically activated gas-filled micropores release hemoglobin and antigens from human erythrocytes in vitro.

作者信息

Miller D L, Lamore B J

出版信息

J Ultrasound Med. 1987 May;6(5):231-6. doi: 10.7863/jum.1987.6.5.231.

DOI:10.7863/jum.1987.6.5.231
PMID:3586116
Abstract

Antigen release from human type B red blood cells was investigated by sensitive capillary-tube assay techniques after subjecting 3% suspensions to a controlled form of ultrasonic cavitation. Cells were kept suspended during the 1,000-sec exposures by an orbital motion of the sample chamber. Several spatial peak intensities of continuous 1.7 MHz ultrasound were applied to the samples which included gas-filled 4-microns diameter micropores in hydrophobic membranes. Free hemoglobin, indicating hemolysis, and free antigenic material, indicating solubilization of antigens, were found in the supernates of suspensions exposed to 90 mW/cm2 or 180 mW/cm2, respectively, or greater intensities. None of the free antigenic material could be attributed to antigen loss by surviving cells. For these conditions, the antigen release effect of ultrasound appears to be a byproduct of cavitation-induced cell lysis.

摘要

采用灵敏的毛细管检测技术,在对3%的悬浮液进行可控形式的超声空化处理后,研究了B型人红细胞的抗原释放情况。在1000秒的暴露过程中,通过样品室的圆周运动使细胞保持悬浮状态。将连续1.7MHz超声的几个空间峰值强度应用于样品,这些样品包括疏水膜中直径为4微米的充气微孔。在分别暴露于90mW/cm²或180mW/cm²或更高强度的悬浮液上清液中,发现了表明溶血的游离血红蛋白和表明抗原溶解的游离抗原物质。没有任何游离抗原物质可归因于存活细胞的抗原损失。在这些条件下,超声的抗原释放效应似乎是空化诱导细胞裂解的副产物。

相似文献

1
Ultrasonically activated gas-filled micropores release hemoglobin and antigens from human erythrocytes in vitro.超声激活的充气微孔在体外从人红细胞中释放血红蛋白和抗原。
J Ultrasound Med. 1987 May;6(5):231-6. doi: 10.7863/jum.1987.6.5.231.
2
The influence of hematocrit on hemolysis by ultrasonically activated gas-filled micropores.血细胞比容对超声激活充气微孔引起溶血的影响。
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Lack of effect of pulsed ultrasound on ABO antigens of human erythrocytes in vitro.脉冲超声对人红细胞ABO抗原的体外作用缺乏效果。
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Further investigations of ATP release from human erythrocytes exposed to ultrasonically activated gas-filled pores.对暴露于超声激活的充气孔隙的人红细胞中ATP释放的进一步研究。
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