7f) In the present study, we screened 85 strains for their abili

7f). In the present study, we screened 85 strains for their ability to induce the in vitro production of IL-12, and L. paracasei MoLac-1 exhibited the highest

ability. In vitro studies using murine splenocytes demonstrated that heat-killed MoLac-1 cells induced the production of IFN-γ by NK cells via stimulation of IL-12 secreted from CD11b+ cells that were probably macrophages (Figs 2-5). Oral administration of heat-killed MoLac-1 increased the proportion of NK cells in spleen Fulvestrant chemical structure (Fig. 6), and ameliorated the symptoms of IFV infection in mice (Fig. 7). The cytokine response of immunocompetent cells to LAB has been reported to be strain dependent (Fujiwara et al., 2004; Medina et al., 2007; Van Hemert et al., 2010). In the NVP-LDE225 research buy present study, more diverse intraspecific distributions of the ability to induce IL-12 were found in L. paracasei, Lactobacillus plantarum,

Lactococcus species, and Streptococcus species than in the other species (Fig. 1). The cell wall of LAB comprises a complex mixture of glycolipids, lipoproteins, and phosphorylated polysaccharides embedded in a thick layer of peptidoglycan (Zeuthen et al., 2008), and it has been suggested that their cell wall structure is involved in their ability to induce IL-12 (Shida et al., 2006b, 2009). These microbial structure characteristics might contribute to the difference of the abilities of strains to induce IL-12. Some studies have reported that IL-12 secretion by LAB stimulation C-X-C chemokine receptor type 7 (CXCR-7) was responsible for IFN-γ production (Shida et al., 2006a; Takeda et al., 2006; Koizumi et al., 2008). In the present experiments, IL-12 and IL-18 were suggested to be involved in the IFN-γ production induced by heat-killed MoLac-1 (Fig. 5), although IL-18 was not detected in the supernatants

in which splenocytes were cultured with MoLac-1 for 2 days (data not shown). It has been reported that NK cells produce large amounts of IFN-γ and that they were activated by high levels of cytotoxicity in response to the combination of IL-12 and IL-18 (Lauwerys et al., 2000). Additionally, it has been reported that human dendritic cells produce IL-18 upon LAB stimulation (Mohamadzadeh et al., 2005). IL-18 at undetectable levels might affect the IFN-γ production induced by heat-killed MoLac-1. It has been reported that some strains of LAB induce IL-12 production by macrophages, monocytes, and dendritic cells and IFN-γ production by NK cells and T cells (Fujiwara et al., 2004; Shida et al., 2006a; Koizumi et al., 2008). In this study, IL-12 production induced by MoLac-1 was diminished CD11b− cells (Fig. 3). CD11b is expressed on various cell populations such as macrophages/monocytes, granulocytes (Ly-6G+), NK cells (DX5+), and subsets of dendritic cells (CD11c+). As Ly-6G− cells, DX5− cells, and CD11c− cells could produce IL-12 induced by MoLac-1, macrophages were considered to be a major source of MoLac-1-induced IL-12 secretion. Furthermore, IFN-γ was mainly produced by activated NK cells (Fig.

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