MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 92 (Suppl.II) December 1997
PAGES: 233-235 DOI: Full paper
Nitric Oxide Mediates the Microbicidal Activity of Eosinophils

Sandra HP Oliveira, Simone G Fonseca, Pedro RT Romão, Sérgio H Ferreira, Fernando Q Cunha+

Departamentos de Farmacologia e Microbiologia, Parasitologia e Imunologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Av. Bandeirantes 900, 14049-900 Ribeirão Preto, SP, Brazil

Abstract

There are several experimental evidences that nitric oxide (NO) is involved in the microbicidal activity of macrophages against a number of intracellular pathogens including Leishmania major, Trypanozoma cruzi, Toxoplasma gondii. It is also well known that eosinophils (EO) have microbicidal activity against many parasites such as Schistosoma mansoni, Trichinella spiralis, T. cruzi and L. amazonensis. The purpose of this study was to investigate if NO is involved in the microbicidal activity of EO against L. major. Eosinophils harvested from peritoneal cavity of rats released spontaneously after 24 and 48 hr a small amount of nitrite. This release was enhanced by the treatment of cells with IFN-g (200 IU/ml). This release was blocked by addition of the NO synthase inhibitor, L-NIO (100 mM) into the culture. To determinate the leishmanicidal activity of eosinophils the parasites were incubated with activated eosinophils with IFN-g and the ability of surviving parasites to incorporate [3H]thymidine was evaluated. IFN-g-activated eosinophils were able to kill L. major and to release high levels of nitrite. The ability to destroy L. major and the release of NO were completely blocked by L-NIO. These results indicate that activated eosinophils release NO which is involved in the microbicidal activity of these cells against L. major.

The microbicidal activity of eosinophils has been associated with degranulation and release of granule-protein such as major basic protein (MBP), eosinophil peroxidase (EPO), eosinophil cationic protein (ECP) and eosinophil-derived neurotoxin (EDN). These substances are cytotoxic to cells and to several parasites in vitro (Gleich et al. 1992), among them, Trichinella spiralis (Wassom & Gleich 1979), Onchocerca volvulus (Greene et al. 1981), Toxocara canis (Badley et al. 1987), Fasciola hepatica (Duffus et al. 1980), Necator americanus (Desakorn et al. 1987), Nippo-strongylus brasiliensis (Kojima et al. 1985), Schistosoma mansoni (Capron et al. 1979, Butterworth et al. 1979), Trypanosoma cruzi (Villalta & Kierszenbaum 1984), Plasmodium falciparum (Waters et al. 1987), Leishmania mexicana amazonensis (Pimenta et al. 1987) and L. donovani (Pearson et al. 1987). In addition to the granule proteins, oxygen-free radicals, including the toxic singlet oxygen, seem to contribute to the microbicidal activity of eosinophils (Pincus et al. 1984).

Nitric oxide (NO) or nitrogen-derived metabolites have been identified as major effector molecules involved in the macrophage microbicidal activity against most intracellular pathogens, including L. major (Liew & Millott 1990), Toxoplasma gondii (Adams et al. 1990), T. musculi (Vincendeau & Dalouede 1991), T. cruzi (Gazzinelli et al. 1992), P. berghei (Mellouk et al. 1991), Mycobacterium leprae (Adams et al. 1991), M. avium (Denis 1991), Candida albicans (Cenci et al. 1993) and the virus Ectromelia, vaccinia and herpes simplex-1 (Gunasegaran et al. 1993). Recently, it was demonstrated that the microbicidal activity of neutrophils against C. albicans is also mediated by NO (Fierro et al. 1996).

Since at present there is no experimental demonstration of the contribution of nitric oxide to the microbicidal activity of eosinophils, the aim of this study was to investigate whether eosinophils produce nitric oxide and whether NO is involved in the microbicidal activity of these cells against L. major.

To investigate if eosinophils are able to produce nitric oxide, these cells were harvested from peritoneal cavities of rats and incubated in vitro with IFN-g. Eosinophils released spontaneously a small amount of nitrite when incubated in vitro. Levels of nitrite in the medium were already present after 12 hr of incubation, which increased continuously within 48 hr. The stimulation of eosinophils with mIFN-g enhanced the release of the nitrite after 24 and 48 hr of incubation. A similar effect of IFN-g has been described in macrophages (Liew & Millott, 1990, Cunha et al. 1993). Nitrite production by the stimulated eosinophils was abolished by the NO synthase inhibitor L-NIO (McCall et al. 1992), indicating that the nitrite measured by the Griess method resulted from the oxidation of L-arginine by NO synthase (Fig. 1).

An important protective role for reactive nitrogen intermediates has been established in macrophage killing of intracellular protozoa (Liew & Millott 1990, Adams et al. 1990, Vincendeau & Dalouede 1991, Gazzinelli et al. 1992), bacteria (Adams et al. 1991, Denis 1991), fungus (Cenci et al. 1993) and virus (Gunasegaran et al. 1993). A similar role has also been demonstrated in neutrophil killing of C. albicans (Fierro et al. 1996) and Staphilococcus aureus (Malawista et al. 1992). Since there are data showing that eosinophils are able to kill Leishmania(Pimenta et al. 1987, Pearson et al. 1987), we investigated whether NO mediates the killing of this intracellular parasite by stimulated eosinophils. IFN-g-activated eosinophils were able to kill L. major and to release high levels of nitrite. The ability to destroy L. major and the release of NO were completely blocked by L-NIO, suggesting that NO mediate the leishmanicidal activity of eosinophils. Leishmania survival inside the unstimulated eosinophils was not affect by L-NIO treatment (Fig. 2). These results, together with the findings that eosinophils are present in Leishmania lesions (Katakura et al. 1993) , reinforce the importance to investigate the role of eosinophils in the evolution of leishmaniasis.

Thus, the data obtained in the present study indicate that activated eosinophils release NO which may be involved in the microbicidal activity of these cells against L. major.

 

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+Corresponding author. Fax: +55-16-633.2301. E-mail:  This e-mail address is being protected from spambots. You need JavaScript enabled to view it.  

Received 3 September 1997

Accepted 30 September 1997

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