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CD62P/CD15s相互作用在血液透析期间白细胞边缘化过程中的主要作用。

A major role for CD62P/CD15s interaction in leukocyte margination during hemodialysis.

作者信息

Stuard S, Carreno M P, Poignet J L, Albertazzi A, Haeffner-Cavaillon N

机构信息

Institut National de la Santé et de la Recherche Médicale, INSERM U430, Hôpital Broussais, Paris, France.

出版信息

Kidney Int. 1995 Jul;48(1):93-102. doi: 10.1038/ki.1995.272.

DOI:10.1038/ki.1995.272
PMID:7564097
Abstract

We investigated expression of several antigens on neutrophils and monocytes, involved in cell adhesion, from patients hemodialyzed with cellulosic and polyacrylonitrile membranes. Among the antigens tested only the expression of CD15s and CD11b was significantly increased on neutrophils and monocytes in patients dialyzed with cellulosic membranes. No changes occurred with polyacrylonitrile membranes. Leukocyte counts from patients dialyzed with cuprophane membranes decreased at the same time as expression of cellular CD15s increased, resulting in a significant negative correlation at all time points tested. No correlation was found between the drop of monocytes and their expression of CD11b. When CD15s expression increased on neutrophils and monocytes, we observed a concomitant increase of CD62P, a specific selectin of activated platelets. When whole blood cells were incubated with complement activated serum both antigens increased but not when cells were incubated with hrC5a. We also observed that CD61, a platelet phenotypic antigen, was present on leukocytes incubated with complement activated serum. At the time when platelet-leukocyte coaggregates decreased, CD62P expression remained stable on leukocytes, suggesting that both neutrophils and monocytes are able to trap either CD62P shed by activated platelets or soluble CD62P present in normal human serum. The present study documents a major role of P-selectin (CD62P)/sialyl-Lewis x (CD15s) interaction in the transient leukocyte margination during hemodialysis.

摘要

我们研究了使用纤维素膜和聚丙烯腈膜进行血液透析的患者中性粒细胞和单核细胞上几种参与细胞黏附的抗原的表达情况。在所检测的抗原中,仅使用纤维素膜透析的患者中性粒细胞和单核细胞上CD15s和CD11b的表达显著增加。使用聚丙烯腈膜时未发生变化。使用铜仿膜透析的患者白细胞计数下降,同时细胞CD15s的表达增加,在所有测试时间点均呈现显著的负相关。未发现单核细胞减少与其CD11b表达之间存在相关性。当中性粒细胞和单核细胞上CD15s表达增加时,我们观察到CD62P(活化血小板的一种特异性选择素)同时增加。当全血细胞与补体激活血清孵育时,两种抗原均增加,但与重组人C5a孵育时则不然。我们还观察到,血小板表型抗原CD61存在于与补体激活血清孵育的白细胞上。在血小板 - 白细胞共聚集减少时,白细胞上CD62P的表达保持稳定,这表明中性粒细胞和单核细胞都能够捕获活化血小板释放的CD62P或正常人血清中存在的可溶性CD62P。本研究证明了P - 选择素(CD62P)/唾液酸化路易斯x(CD15s)相互作用在血液透析期间短暂的白细胞边缘化过程中起主要作用。

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