LPS is a component of gram-negative bacteria outer-membrane that binds TLR-4. Well known for its pro-inflammatory properties it also dampens immune responses in various experimental setups (e.g. [39, 46, 47]). To test whether Treg are directly involved in the mechanism at the basis of the ‘hygiene hypothesis’, we first tested various protocols of LPS administration selleck chemical for their capacity to prevent diabetes occurrence in NOD mice. Next, by conducting cellular analysis we revealed that LPS treatment enhances Treg numbers and activity. Finally, by performing adoptive transfer experiments we demonstrated that CD25-expressing Treg are involved in the beneficial effect of LPS

in NOD mice, thus providing evidence that CD25+ Treg may play a central role

in the cellular mechanism at the basis of the ‘hygiene hypothesis’. Mice.  Non-obese diabetic (NOD)/Lt and NOD/SCID mice were originally purchased from The Jackson Laboratory (Bar Harbor, ME, USA). All animals were bred and maintained under specific pathogen-free conditions in our animal facilities. Mice experimental protocols were approved by the Instituto Gulbenkian de Ciência ethics committee and by the national authority Direcção Geral de Veterinária. LPS treatment.  In most experiments, 6- to 8-week-old NOD mice were injected i.p. with 10 μg LPS from Salmonella typhimurium (Sigma, Sintra, Portugal) diluted in PBS, once per week until the buy GSK458 time of analysis. Other experimental groups were: 12-week-old NOD females injected weekly with 10 μg LPS i.p. until time of analysis; 7.5 weeks of age NOD females injected once with 10 μg LPS and 4 weeks of age NOD females injected every 3 days with 10 μg LPS i.p., Astemizole during 1 month. In all experimental groups, PBS-injected age-matched animals served as controls. Diabetes detection.  Diabetes was monitored weekly or biweekly, according to the experiment, by measuring blood glucose levels using ACCU-CHEK Sensor Comfort strips (Roche, Mannheim, Germany). Mice that had values ≥250 mg/dl on two consecutive occasions were deemed diabetic. Cell purification and FACS analysis.  For flow cytometry purification,

thymus, pancreatic (p)LN or spleen cells, according to the experiment, were obtained by forcing the organs through a 100 μm nylon mesh. For isolation of pancreas-infiltrating lymphocytes, whole pancreas (after careful removal of pLN used in the same experiment for FACS staining) were cut into small pieces and incubated in OptiMEM medium (Invitrogen, Madrid, Spain) containing 5% FCS and 450 U of collagenase (Sigma) for 20 min at 37 °C. After filtering through 100 μm nylon mesh, lymphoid cells were isolated on a 40% Percoll gradient. The cells were then washed for posterior FACS staining. For FACS staining, 1 × 106 cells (whenever possible) were preincubated for 20 min with unlabelled mAb to the Fc-γ receptor (clone 2.