Abstract:
:In mice, nitric oxide (NO) production by inducible NO synthase (iNOS), is a component of the control of Brucella infection. In humans, the involvement of iNOS in infection is still a matter of debate. Based on in vitro experiments, it was recently postulated that in humans, Brucella infection tends to become chronic because NO cannot exert its deleterious effect. In fact, conditions allowing NO production by human macrophages in culture are poorly defined, rendering the in vitro study of NO function difficult. Using DFGiNOS U937 macrophagic cells engineered to produce NO and U937 cells activated by ligation of IgE receptors, we showed that the intracellular development of Brucella was impaired in human macrophages, which produced NO. Although Brucella-infected human macrophagic phagocytes did not release NO in commonly used models of infection, the machinery required to produce NO was expressed in these cells and could be triggered by cell membrane receptors present on the infected cells. Therefore, the lack of NO production in isolated human macrophages infected by Brucella under in vitro conditions did not exclude a possible involvement of NO in the control of human brucellosis.
journal_name
Microb Pathogjournal_title
Microbial pathogenesisauthors
Gross A,Bertholet S,Mauel J,Dornand Jdoi
10.1016/j.micpath.2003.09.003subject
Has Abstractpub_date
2004-02-01 00:00:00pages
75-82issue
2eissn
0882-4010issn
1096-1208pii
S0882401003001827journal_volume
36pub_type
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journal_title:Microbial pathogenesis
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journal_title:Microbial pathogenesis
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