shifts macrophage polarization toward M1-like phenotype with an altered cytokine profile.

: The macrophage is an innate immune defense cell involved in pathogen recognition and clearance. : In view of the diversity of the macrophage phenotype and function, the present study investigated how infection affects the differentiation, phenotype and cytokine profile of macrophages. : Murine bone marrow-derived stem cells were co-cultured with before and after differentiation. Macrophage M0 polarization towards M1 or M2 was initiated at day 6 by addition of LPS and INF-γ, or IL-4 and IL-13, respectively. : did not inhibit macrophage differentiation and were identified within macrophages. Viability of the macrophages infected with prior to differentiation was enhanced, evidenced by apoptosis inhibition, as was expression of CD38 and IRF5 proteins, indicators of M1-like polarization. These M1-like macrophages expressed an aberrant cytokine mRNA profile, with reduction in inflammatory cytokines IL-1β and IL-12 and increase in regulatory cytokine IL-10. No changes in TNF-α or TGF-β1 were detected, compared with the control groups. This atypical M1-like phenotype was retained even upon stimulation with growth factors that normally trigger their development into M2 macrophages. : These findings suggested that infection of bone marrow-derived stem cells during differentiation into macrophages induces an atypical M1-like phenotype associated with intracellular bacterial survival.