Combined regulation of pro-inflammatory cytokines production by STAT3 and STAT5 in a model of infection of alveolar macrophages.

is a highly contagious respiratory pathogen responsible for whooping-cough or pertussis. Despite high vaccination coverage worldwide, this gram-negative bacterium continues to spread among the population. is transmitted by aerosol droplets from an infected individual to a new host and will colonize its upper respiratory tract. Alveolar macrophages (AMs) are effector cells of the innate immune system that phagocytose and secrete both pro-inflammatory and antimicrobial mediators in the lungs. However, understanding their role in pathogenesis at the molecular level is hampered by the limited number of primary AMs that can be collected . In order to decipher the regulation of innate response induced by infection, we used for the first time self-renewing, non-transformed cells, called Max Planck Institute (MPI) cells, which are phenotypically and functionally very close to pulmonary AMs. Using optimized infection conditions, we characterized the entry and the clearance of within MPI macrophages. We showed that under these conditions, MPI cells exhibit a pro-inflammatory phenotype with the production of TNF, IL-1β, IL-6 and MIP-2α, similarly to primary AMs purified from broncho-alveolar fluids of mice. In addition, we explored the yet uncharacterized role of the signal transduction activator of transcription (STAT) proteins family in the innate immune response to infection and showed for the first time the parallel regulation of pro-inflammatory cytokines by STAT3 and STAT5 in MPI macrophages infected by . Altogether, this work highlights the interest of using MPI cells for experiments optimization and preliminary data acquisition to understand interaction with AMs, and thus significantly reduce the number of animals to be sacrificed.