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The Journal of Immunology, 1999, 162: 3519-3526.
Copyright © 1999 by The American Association of Immunologists

Modulation of Endocytosis in Nuclear Factor IL-6(-/-) Macrophages Is Responsible for a High Susceptibility to Intracellular Bacterial Infection1

Javier Pizarro-Cerdá*, Michel Desjardins{dagger}, Edgardo Moreno{ddagger}, Shizuo Akira§ and Jean-Pierre Gorvel2,*

* Centre d’Immunologie de Marseille-Luminy, Marseille, France; {dagger} Département d’Anatomie, Université de Montréal, Québec, Canada; {ddagger} Programa de Investigación en Enfermedades Tropicales, Universidad Nacional, Heredia, Costa Rica; and § Hyogo College of Medicine, Nishinomiya, Hyogo, Japan

Activated macrophages kill bacteria, a function known to depend on the expression of NF-IL-6. Here, it is demonstrated that the attenuated Brucella abortus vaccine strain 19 replicates much better in NF-IL-6-/- than in NF-IL-6(+/+) and NF-IL-6(+/+)-activated murine macrophages and at levels comparable to those observed in normal macrophages infected with the pathogenic strain 2308. The role of NF-IL-6 in the inhibition of intracellular bacterial replication is related to its control of endocytosis and membrane fusion between endosomes and Brucella-containing phagosomes. Addition of the granulocyte-CSF (G-CSF), whose induction is impaired in NF-IL-6(-/-) macrophages, restores both endocytosis and the morphology of endosomes, together with bactericidal activity. Regulation of membrane traffic in endocytosis by G-CSF whose expression is controlled by NF-IL-6 may explain how a host cell can control intracellular bacterial replication.




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