PMID- 20625918 OWN - NLM STAT- MEDLINE DCOM- 20110429 LR - 20211020 IS - 1420-908X (Electronic) IS - 1023-3830 (Linking) VI - 60 IP - 1 DP - 2011 Jan TI - IgE-dependent sensitization increases responsiveness to LPS but does not modify development of endotoxin tolerance in mast cells. PG - 19-27 LID - 10.1007/s00011-010-0230-4 [doi] AB - OBJECTIVE: Effects of immunoglobulin E (IgE)-dependent sensitization on the response to bacterial lipopolysaccharide (LPS) were analyzed in mast cells. METHODS: Murine bone marrow-derived mast cells (BMMCs) were sensitized or not with IgE before stimulation with LPS. TLR4 and co-receptors expression was analyzed by flow cytometry and RT-PCR, TNF-alpha production by ELISA, IKK and IkappaB activation by western blot or immunoprecipitation. NFkappaB nuclear translocation was determined by EMSA. RESULTS: IgE-sensitized BMMCs secreted larger amounts of TNF-alpha than non-sensitized cells shortly after LPS challenge. No change in TLR4, CD14 or MD-2 expression was detected after the IgE-dependent sensitization process, whereas TLR4-dependent phosphorylation of IKK and IkappaB was augmented. IgE-dependent sensitization increased basal NFkappaB activity. Endotoxin tolerance was not affected by the IgE-dependent sensitization process. CONCLUSIONS: IgE-induced sensitization primes mast cells for higher response to LPS through pre-activation of NFkappaB transcription factor. IgE-dependent sensitization does not modify events leading to endotoxin tolerance. FAU - Medina-Tamayo, Jaciel AU - Medina-Tamayo J AD - Departamento de Farmacobiologia, Centro de Investigacion y de Estudios Avanzados del IPN, Sede Sur, Calzada de los Tenorios No 235, Col Granjas Coapa, Tlalpan, Mexico, DF, Mexico. FAU - Ibarra-Sanchez, Alfredo AU - Ibarra-Sanchez A FAU - Padilla-Trejo, Alejandro AU - Padilla-Trejo A FAU - Gonzalez-Espinosa, Claudia AU - Gonzalez-Espinosa C LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100713 PL - Switzerland TA - Inflamm Res JT - Inflammation research : official journal of the European Histamine Research Society ... [et al.] JID - 9508160 RN - 0 (BAY 11-7085) RN - 0 (Lipopolysaccharides) RN - 0 (NF-kappa B) RN - 0 (Nitriles) RN - 0 (Sulfones) RN - 0 (Toll-Like Receptor 4) RN - 0 (Tumor Necrosis Factor-alpha) RN - 37341-29-0 (Immunoglobulin E) RN - EC 2.7.11.10 (I-kappa B Kinase) SB - IM MH - Active Transport, Cell Nucleus MH - Animals MH - Bone Marrow Cells/cytology/immunology MH - Cells, Cultured MH - I-kappa B Kinase/metabolism MH - Immune Tolerance/*immunology MH - Immunoglobulin E/*immunology MH - Lipopolysaccharides/*immunology/pharmacology MH - Mast Cells/cytology/drug effects/*immunology MH - Mice MH - NF-kappa B/antagonists & inhibitors/metabolism MH - Nitriles MH - Sulfones MH - Toll-Like Receptor 4/genetics/metabolism MH - Tumor Necrosis Factor-alpha/genetics/immunology EDAT- 2010/07/14 06:00 MHDA- 2011/04/30 06:00 CRDT- 2010/07/14 06:00 PHST- 2010/04/06 00:00 [received] PHST- 2010/06/23 00:00 [accepted] PHST- 2010/06/08 00:00 [revised] PHST- 2010/07/14 06:00 [entrez] PHST- 2010/07/14 06:00 [pubmed] PHST- 2011/04/30 06:00 [medline] AID - 10.1007/s00011-010-0230-4 [doi] PST - ppublish SO - Inflamm Res. 2011 Jan;60(1):19-27. doi: 10.1007/s00011-010-0230-4. Epub 2010 Jul 13.