PMID- 19494521 OWN - NLM STAT- MEDLINE DCOM- 20091229 LR - 20111117 IS - 1423-0097 (Electronic) IS - 1018-2438 (Linking) VI - 150 IP - 3 DP - 2009 TI - Differential protein expression by dendritic cells from atopic and non-atopic individuals after stimulation by the major house dust mite allergen Der p 1. PG - 237-51 LID - 10.1159/000222676 [doi] AB - BACKGROUND: Dendritic cells (DCs) are sentinels of the immune system and are known to play a key role in allergic responses. However, it is not clear how DCs that have been exposed to an allergen support Th2 type immune responses. It is possible that DCs from atopic individuals are inherently programmed to support allergic disease, or it is the exposure of dendritic cells to allergens that is key to the development of allergic sensitisation. METHODS: We used 2D gel electrophoresis and MALDI mass spectrometry to compare the proteome of DCs from atopic and non-atopic individuals in both the resting state and after stimulation with the major house dust mite allergen Der p 1. RESULTS: Our data show that unstimulated DCs from atopic and non-atopic individuals are very similar at the whole cell proteome level, showing few differentially expressed proteins. However, upon stimulation with Der p 1, a number of additional proteins are differentially expressed, and of these several were of potential relevance to Th2 cell differentiation and the allergic response, including GTP-binding regulatory protein Gi alpha-2, frabin and cathepsin D. CONCLUSION: Whilst there are inherent differences between DCs from atopic and non-atopic individuals, it seems that exposure to allergen plays a key role in differential expression of proteins by these key immune cells. Further studies should now focus on establishing the biological relevance of these proteins as biomarkers in house dust mite allergy and their role in allergen induced Th2 cell differentiation. CI - Copyright 2009 S. Karger AG, Basel. FAU - Horlock, C AU - Horlock C AD - Institute of Infection, Immunity and Inflammation, School of Molecular Medical Sciences and Biomedical Research Unit, University of Nottingham, Nottingham, UK. FAU - Shakib, F AU - Shakib F FAU - Jones, N S AU - Jones NS FAU - Sewell, H F AU - Sewell HF FAU - Ghaemmaghami, A M AU - Ghaemmaghami AM LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090604 PL - Switzerland TA - Int Arch Allergy Immunol JT - International archives of allergy and immunology JID - 9211652 RN - 0 (Allergens) RN - 0 (Antigens, Dermatophagoides) RN - 0 (Arthropod Proteins) RN - 0 (FGD4 protein, human) RN - 0 (Microfilament Proteins) RN - 0 (Proteome) RN - EC 3.4.22.- (Cysteine Endopeptidases) RN - EC 3.4.22.- (Dermatophagoides pteronyssinus antigen p 1) RN - EC 3.4.23.5 (Cathepsin D) RN - EC 3.6.5.1 (GTP-Binding Protein alpha Subunits, Gi-Go) SB - IM MH - Adult MH - Allergens/*immunology MH - Animals MH - Antigens, Dermatophagoides/*immunology MH - Arthropod Proteins MH - Cathepsin D/genetics/immunology/metabolism MH - Cells, Cultured MH - Cysteine Endopeptidases MH - Dendritic Cells/immunology/*metabolism/pathology MH - Electrophoresis, Gel, Two-Dimensional MH - Female MH - GTP-Binding Protein alpha Subunits, Gi-Go/genetics/immunology/metabolism MH - Gene Expression Profiling MH - Humans MH - Hypersensitivity, Immediate/genetics/*immunology/*metabolism/pathology MH - Male MH - Microfilament Proteins/genetics/immunology/metabolism MH - Middle Aged MH - Proteome MH - Pyroglyphidae/immunology MH - Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization MH - Th2 Cells/immunology EDAT- 2009/06/06 09:00 MHDA- 2009/12/30 06:00 CRDT- 2009/06/05 09:00 PHST- 2008/09/30 00:00 [received] PHST- 2009/02/16 00:00 [accepted] PHST- 2009/06/05 09:00 [entrez] PHST- 2009/06/06 09:00 [pubmed] PHST- 2009/12/30 06:00 [medline] AID - 000222676 [pii] AID - 10.1159/000222676 [doi] PST - ppublish SO - Int Arch Allergy Immunol. 2009;150(3):237-51. doi: 10.1159/000222676. Epub 2009 Jun 4.