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人类多形核白细胞对抗菌防御素的细胞外释放。

Extracellular release of antimicrobial defensins by human polymorphonuclear leukocytes.

作者信息

Ganz T

出版信息

Infect Immun. 1987 Mar;55(3):568-71. doi: 10.1128/iai.55.3.568-571.1987.

Abstract

Human polymorphonuclear leukocytes (PMN) contain three antimicrobial and cytotoxic peptides which belong to a family of mammalian granulocyte peptides named defensins. To determine their potential availability for extracellular microbicidal or cytotoxic events, we quantified the extracellular release of defensins after stimulation of human PMN with phorbol myristate acetate and opsonized zymosan. As determined by enzyme immunoassay and confirmed by polyacrylamide gel electrophoresis and densitometry, 10(6) human PMN contained 4 to 5 micrograms of defensins. After stimulation with a high concentration of phorbol myristate acetate (1 microgram/ml), about 8% of PMN defensins were found in the media. Release of defensins correlated best with the release of azurophil granule marker beta-glucuronidase or elastase and poorly with the release of either the specific granule marker lactoferrin or cytoplasmic lactate dehydrogenase. Phagocytosis of opsonized zymosan resulted in the extracellular release of less than 3% of PMN defensins. The factors responsible for less release of defensins into media relative to the release of other azurophil granule proteins may include heterogeneity of azurophil granules and the affinity of defensins for cellular surfaces and opsonized particles. In vivo, defensins are most likely to reach effective microbicidal or cytotoxic concentrations in PMN-rich exudates (pus), in confined environments of the phagolysosomes, or in intercellular clefts between PMN and their targets.

摘要

人类多形核白细胞(PMN)含有三种抗菌和细胞毒性肽,它们属于名为防御素的哺乳动物粒细胞肽家族。为了确定它们在细胞外杀菌或细胞毒性事件中的潜在可用性,我们在用佛波酯肉豆蔻酸酯乙酸盐和调理酵母聚糖刺激人类PMN后,对防御素的细胞外释放进行了定量。通过酶免疫测定确定,并经聚丙烯酰胺凝胶电泳和光密度测定证实,10⁶个人类PMN含有4至5微克防御素。在用高浓度佛波酯肉豆蔻酸酯乙酸盐(1微克/毫升)刺激后,约8%的PMN防御素出现在培养基中。防御素的释放与嗜天青颗粒标志物β-葡萄糖醛酸酶或弹性蛋白酶的释放相关性最好,而与特异性颗粒标志物乳铁蛋白或细胞质乳酸脱氢酶的释放相关性较差。调理酵母聚糖的吞噬作用导致PMN防御素的细胞外释放少于3%。相对于其他嗜天青颗粒蛋白的释放,防御素向培养基中释放较少的原因可能包括嗜天青颗粒的异质性以及防御素对细胞表面和调理颗粒的亲和力。在体内,防御素最有可能在富含PMN的渗出液(脓液)、吞噬溶酶体的受限环境或PMN与其靶标之间的细胞间隙中达到有效的杀菌或细胞毒性浓度。

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