Removing the charges of the basic amino-acid residues of melittin prevents pore formation. It was also found that in the absence of counter ions pores not only form more rapidly but lead to membrane rupture. The rupture process occurs via a novel recursive potation pathway, which we coin the Droste mechanism. (c) 2008 Elsevier B.V. All rights reserved.”
“Dendritic cells (DCs), which are biased toward a tolerogenic profile, play a pivotal role in tissue-remodeling processes and angiogenesis at the maternalfetal interface. Here, we analyzed the effect of trophoblast cells on the functional

profile of DCs to gain insight on the tolerogenic mechanisms underlying the human placentalmaternal dialog Trichostatin A ic50 at early stages of gestation.\n\nDCs were differentiated from peripheral blood monocytes obtained from fertile women (n 21), in the presence of interleukin (IL)-4 and granulocyte-macrophage colony-stimulating factor during 5 days in culture. Then, DCs were cultured with trophoblast cells (Swan-71 cell line obtained from normal cytotrophoblast, at 7 weeks) for 24 h and for an additional 24 h in the

absence or presence of lipopolysaccharide (LPS) from Escherichia coli. DCs were recovered and used for flow cytometry, enzyme-linked immunosorbent assay, RTPCR and suppression and migration assays.\n\nTrophoblast cells significantly prevented the increase in CD83 expression induced by LPS without affecting the expression of CD86, CD40 and human leukocyte BI 2536 order antigen-DR (P 0.05). Trophoblast cells signifinatly decreased the production of IL-12p70 and tumor necrosis factor-, while it increased the production of IL-10

(P 0.05). No changes were observed in the production of IL-6 and monocyte chemotactic protein-1. The culture of DCs with trophoblast cells, also suppressed the stimulation of the allogeneic response triggered by LPS (P 0.05). Conditioned DCs were able to increase the frequency of CD4 CD25 Foxp3 cells and this effect was accompanied by an increase in indoleamine 2, 3-dioxygenase Immunology & Inflammation inhibitor expression in DCs (P 0.05).\n\nThe interaction of DCs with trophoblast cells promotes the differentiation of DCs into cells with a predominantly tolerogenic profile that could contribute to a tolerogenic microenvironment at the maternalfetal interface.”
“Background: We have previously demonstrated that Lactobacillus casei CRL 431 administration improved the resistance to pneumococcal infection in a mouse model.\n\nMethods: This study examined the effects of the oral administration of Lactobacillus casei CRL 431 (L. casei) on the activation of coagulation and fibrinolytic systems as well as their inhibitors during a Streptococcus pneumoniae infection in mice.\n\nResults: The alveolo-capillary membrane was damaged and the coagulation system was also activated by the infection.

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