Defensins. Natural peptide antibiotics of human neutrophils.
Open Access
- 1 October 1985
- journal article
- research article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 76 (4) , 1427-1435
- https://doi.org/10.1172/jci112120
Abstract
We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-3, and which will be referred to as "defensins." HNP 1-3, a mixture of the three defensins, killed Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli effectively in vitro when tested in 10 mM phosphate buffer containing certain nutrients, but it had little or no bactericidal activity in nutrient-free buffer. In contrast, the nutrient-free buffer supported a high degree of activity by HNP 1-3 against Cryptococcus neoformans. In addition to its antibacterial and antifungal properties, HNP 1-3 directly inactivated herpes simplex virus, Type 1. Two of the individual purified defensins, HNP-1 and HNP-2, were as microbicidal as the mixture HNP 1-3. HNP-3 was less active than the other defensins against most but not all of the microbes tested. Immunoperoxidase stains revealed HNP 1-3 to have a granular localization in the neutrophil's cytoplasm by light microscopy. Frozen thin section immunogold transmission electron microscopy showed HNP 1-3 to be localized in azurophil granules. These studies define a broad-spectrum antimicrobial system in human neutrophils. The defensin system may operate in conjunction with or independently from oxygen-dependent microbicidal processes to enable human neutrophils to inactivate and destroy potential pathogens.This publication has 60 references indexed in Scilit:
- Primary structures of three human neutrophil defensins.Journal of Clinical Investigation, 1985
- Killing Capacity of Human Polymorphonuclear Leukocytes in Aerobic and Anaerobic ConditionsJournal of Medical Microbiology, 1984
- Characterization of two crystal forms of neutrophil cationic protein NP2, a naturally occurring broad-spectrum antimicrobial agent from leukocytesJournal of Molecular Biology, 1984
- Redistribution of alpha-granules and their contents in thrombin-stimulated platelets.The Journal of cell biology, 1984
- A Bactericidal Effect for Human LactoferrinScience, 1977
- Antibacterial activity of cationic proteins from human granulocytes.Journal of Clinical Investigation, 1975
- Functional Aspects of a Second Mechanism of Candidacidal Activity by Human NeutrophilsJournal of Clinical Investigation, 1972
- THE DEVELOPMENT OF NEUTROPHILIC POLYMORPHONUCLEAR LEUKOCYTES IN HUMAN BONE MARROWThe Journal of Experimental Medicine, 1971
- Natural Host Resistance to Infection with Cryptococcus neoformans: IV. The Effect of Some Cationic Proteins on the Experimental DiseaseThe Journal of Infectious Diseases, 1966
- PHAGOCYTIN: A BACTERICIDAL SUBSTANCE FROM POLYMORPHONUCLEAR LEUCOCYTESThe Journal of Experimental Medicine, 1956