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人类单核细胞不同功能特性之间的关系。

Relationships between different functional properties of human monocytes.

作者信息

Gill P G, Waller C A, MacClennan I C

出版信息

Immunology. 1977 Dec;33(6):873-80.

Abstract

Various methods for measuring monocyte numbers and function in human blood are compared. The assays used were: phagocytosis of antibody-sensitized sheep red cells; staining for diffuse non-specific esterase activity; capacity to adhere to polystyrene and ability to lyse human A1 red cells sensitized with allogeneic anti-A1 antibody. The following conclusions are drawn from the results: (1) Previous observations showing that sensitized A1 red cells are lysed by phagocytic cells and not K cells are confirmed. (2) Granulocytes lyse sensitized A1 red cells more rapidly than monocytes and this assay is only useful for assessing monocyte function if granulocytes are first removed from preparations. (3) Phagocytosis is important in the lysis of sensitized A1 red cells by monocytes. (4) Esterase positive cells correlate significantly with the number of cells phagocytosing sensitized sheep red blood cells, r = 0.83 (P less than 0.001) and with the number of cells adhering to polystyrene, r = 0.53 (P less than 0.05). (5) The lysis of sensitized A1 red cells correlated significantly with esterase positive cell numbers, r = 0.57 (P less than 0.001) and phagocytosis of sensitized sheep red cells, r = 0.50 (P less than 0.01 but not with the numbers of adherent cells, r = 0.34 (P greater than 0.05).

摘要

对测量人体血液中单核细胞数量和功能的各种方法进行了比较。所使用的检测方法有:吞噬抗体致敏的绵羊红细胞;检测弥漫性非特异性酯酶活性;黏附于聚苯乙烯的能力以及裂解经同种异体抗A1抗体致敏的人A1红细胞的能力。从结果中得出以下结论:(1)先前的观察结果表明致敏的A1红细胞是被吞噬细胞而非K细胞裂解,这一结论得到了证实。(2)粒细胞裂解致敏A1红细胞的速度比单核细胞快,只有在首先从样本中去除粒细胞后,该检测方法才对评估单核细胞功能有用。(3)吞噬作用在单核细胞裂解致敏A1红细胞过程中很重要。(4)酯酶阳性细胞与吞噬致敏绵羊红细胞的细胞数量显著相关,r = 0.83(P小于0.001),与黏附于聚苯乙烯的细胞数量相关,r = 0.53(P小于0.05)。(5)致敏A1红细胞的裂解与酯酶阳性细胞数量显著相关,r = 0.57(P小于0.001),与致敏绵羊红细胞的吞噬作用相关,r = 0.50(P小于0.01),但与黏附细胞数量无关,r = 0.34(P大于0.05)。

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Antibody-induced hemolytic activity of human blood monocytes.人血单核细胞的抗体诱导溶血活性。
Scand J Immunol. 1974;3(2):173-80. doi: 10.1111/j.1365-3083.1974.tb01245.x.

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