Technical Advance: Platelet-neutrophil complex formation-a detailed in vitro analysis of murine and human blood samples

被引:28
|
作者
Mauler, Maximilian [1 ,2 ]
Seyfert, Julia [2 ]
Haenel, David [2 ]
Seeba, Hannah [2 ]
Guenther, Janine [2 ]
Stallmann, Daniela [2 ]
Schoenichen, Claudia [2 ]
Hilgendorf, Ingo [2 ]
Bode, Christoph [2 ]
Ahrens, Ingo [2 ]
Duerschmied, Daniel [2 ]
机构
[1] Univ Freiburg, Fac Biol, Hugstetter Str 55, D-79106 Freiburg, Germany
[2] Univ Freiburg, Ctr Heart, Dept Cardiol & Angiol 1, Hugstetter Str 55, D-79106 Freiburg, Germany
关键词
P-selectin; flow cytometry; platelet activation; P-SELECTIN; LEUKOCYTE RECRUITMENT; ACTIVATION; REPERFUSION; MONOCYTES; ISCHEMIA; BINDING; MOUSE; COUNT; MICE;
D O I
10.1189/jlb.3TA0315-082R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Platelets form complexes with neutrophils during inflammatory processes. These aggregates migrate into affected tissues and also circulate within the organism. Several studies have evaluated platelet-neutrophil complexes as a marker of cardiovascular diseases in human and mouse. Although multiple publications have reported platelet-neutrophil complex counts, we noticed that different methods were used to analyze platelet-neutrophil complex formation, resulting in significant differences, even in baseline values. We established a protocol for platelet-neutrophil complex measurement with flow cytometry in murine and human whole blood samples. In vitro platelet-neutrophil complex formation was stimulated with ADP or PMA. We tested the effect of different sample preparation steps and cytometer settings on platelet-neutrophil complex detection and noticed false-positive counts with increasing acquisition speed. Platelet-neutrophil complex formation depends on platelet P-selectin expression, and antibody blocking of P-selectin consequently prevented ADP-induced platelet-neutrophil complex formation. These findings may help generating more comparable data among different research groups that examine platelet-neutrophil complexes as a marker for cardiovascular disease and novel therapeutic interventions.
引用
收藏
页码:781 / 789
页数:9
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