-
Something wrong with this record ?
The Role of Alveolar Epithelial Type II-Like Cells in Uptake of Structurally Different Antigens and in Polarisation of Local Immune Responses
J. Akgün, I. Schabussova, M. Schwarzer, H. Kozakova, M. Kundi, U. Wiedermann,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 2006
Free Medical Journals
from 2006
Public Library of Science (PLoS)
from 2006
PubMed Central
from 2006
Europe PubMed Central
from 2006
ProQuest Central
from 2006-12-01
Open Access Digital Library
from 2006-10-01
Open Access Digital Library
from 2006-01-01
Open Access Digital Library
from 2006-01-01
Medline Complete (EBSCOhost)
from 2008-01-01
Nursing & Allied Health Database (ProQuest)
from 2006-12-01
Health & Medicine (ProQuest)
from 2006-12-01
Public Health Database (ProQuest)
from 2006-12-01
ROAD: Directory of Open Access Scholarly Resources
from 2006
- MeSH
- Allergens metabolism MeSH
- Hypersensitivity MeSH
- Antigens, Plant chemistry MeSH
- Antigens metabolism MeSH
- Cytokines metabolism MeSH
- Respiratory System immunology MeSH
- Epithelial Cells cytology MeSH
- Epitopes, T-Lymphocyte chemistry MeSH
- Epitopes chemistry MeSH
- Phenotype MeSH
- Fluoresceins chemistry MeSH
- Immune System MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Mice, Inbred BALB C MeSH
- Mice MeSH
- Pulmonary Alveoli cytology MeSH
- Flow Cytometry MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: Our previous studies on intranasal tolerance induction demonstrated reduction of allergic responses with different allergen constructs. The underlying mechanisms varied depending on their conformation or size. OBJECTIVE: The aim of the present study was to compare the uptake of two structurally different allergen molecules within the respiratory tract following intranasal application. METHODS: The three-dimensional Bet v 1 (Bv1-Protein) and the T cell epitope peptide of Bet v 1 (Bv1-Peptide) were labelled with 5,6-Carboxyfluorescein (FAM) and their uptake was investigated in lung cells and cells of the nasal associated lymphoid tissue from naive and sensitised BALB/c mice. Phenotypic characterisation of FAM+ lung cells after antigen incubation in vitro and after intranasal application was performed by flow cytometry. Impact of Bv1-Protein and Bv1-Peptide on cytokine profiles and gene expression in vivo or in an alveolar epithelial type II (ATII) cell line were assessed in mono- and co-cultures with monocytes using ELISA and quantitative real-time PCR. RESULTS: Both antigens were taken up preferably by ATII-like cells (ATII-LCs) in naive mice, and by macrophages in sensitised mice. After intranasal application, Bv1-Peptide was taken up faster and more efficiently than Bv1-Protein. In vivo and in vitro experiments revealed that Bv1-Protein induced the transcription of thymic stromal lymphopoietin mRNA while Bv1-Peptide induced the transcription of IL-10 and MCP1 mRNA in ATII-LCs. CONCLUSION AND CLINICAL RELEVANCE: Both tested antigens were taken up by ATII-LCs under steady state conditions and induced different polarisation of the immune responses. These data may have an important impact for the generation of novel and more effective prophylactic or therapeutic tools targeting the respiratory mucosa.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16010298
- 003
- CZ-PrNML
- 005
- 20160408112313.0
- 007
- ta
- 008
- 160408s2015 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1371/journal.pone.0124777 $2 doi
- 024 7_
- $a 10.1371/journal.pone.0124777 $2 doi
- 035 __
- $a (PubMed)25894334
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Akgün, Johnnie $u Institute of Specific Prophylaxis and Tropical Medicine, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria. $7 gn_A_00002884
- 245 14
- $a The Role of Alveolar Epithelial Type II-Like Cells in Uptake of Structurally Different Antigens and in Polarisation of Local Immune Responses / $c J. Akgün, I. Schabussova, M. Schwarzer, H. Kozakova, M. Kundi, U. Wiedermann,
- 520 9_
- $a BACKGROUND: Our previous studies on intranasal tolerance induction demonstrated reduction of allergic responses with different allergen constructs. The underlying mechanisms varied depending on their conformation or size. OBJECTIVE: The aim of the present study was to compare the uptake of two structurally different allergen molecules within the respiratory tract following intranasal application. METHODS: The three-dimensional Bet v 1 (Bv1-Protein) and the T cell epitope peptide of Bet v 1 (Bv1-Peptide) were labelled with 5,6-Carboxyfluorescein (FAM) and their uptake was investigated in lung cells and cells of the nasal associated lymphoid tissue from naive and sensitised BALB/c mice. Phenotypic characterisation of FAM+ lung cells after antigen incubation in vitro and after intranasal application was performed by flow cytometry. Impact of Bv1-Protein and Bv1-Peptide on cytokine profiles and gene expression in vivo or in an alveolar epithelial type II (ATII) cell line were assessed in mono- and co-cultures with monocytes using ELISA and quantitative real-time PCR. RESULTS: Both antigens were taken up preferably by ATII-like cells (ATII-LCs) in naive mice, and by macrophages in sensitised mice. After intranasal application, Bv1-Peptide was taken up faster and more efficiently than Bv1-Protein. In vivo and in vitro experiments revealed that Bv1-Protein induced the transcription of thymic stromal lymphopoietin mRNA while Bv1-Peptide induced the transcription of IL-10 and MCP1 mRNA in ATII-LCs. CONCLUSION AND CLINICAL RELEVANCE: Both tested antigens were taken up by ATII-LCs under steady state conditions and induced different polarisation of the immune responses. These data may have an important impact for the generation of novel and more effective prophylactic or therapeutic tools targeting the respiratory mucosa.
- 650 _2
- $a alergeny $x metabolismus $7 D000485
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a antigeny $x metabolismus $7 D000941
- 650 _2
- $a antigeny rostlinné $x chemie $7 D052179
- 650 _2
- $a cytokiny $x metabolismus $7 D016207
- 650 _2
- $a epitelové buňky $x cytologie $7 D004847
- 650 _2
- $a epitopy $x chemie $7 D000939
- 650 _2
- $a epitopy T-lymfocytární $x chemie $7 D018984
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a fluoresceiny $x chemie $7 D005452
- 650 _2
- $a alergie $7 D006967
- 650 _2
- $a imunitní systém $7 D007107
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední BALB C $7 D008807
- 650 _2
- $a fenotyp $7 D010641
- 650 _2
- $a plicní alveoly $x cytologie $7 D011650
- 650 _2
- $a kvantitativní polymerázová řetězová reakce $7 D060888
- 650 _2
- $a dýchací soustava $x imunologie $7 D012137
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Schabussova, Irma $u Institute of Specific Prophylaxis and Tropical Medicine, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Schwarzer, Martin $u Laboratory of Gnotobiology, Institute of Microbiology, v.v.i., Academy of Sciences of the Czech Republic, Novy Hradek, Czech Republic.
- 700 1_
- $a Kozakova, Hana $u Laboratory of Gnotobiology, Institute of Microbiology, v.v.i., Academy of Sciences of the Czech Republic, Novy Hradek, Czech Republic.
- 700 1_
- $a Kundi, Michael $u Institute of Environmental Health, Medical University of Vienna, Vienna, Austria.
- 700 1_
- $a Wiedermann, Ursula $u Institute of Specific Prophylaxis and Tropical Medicine, Centre for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria; Department of Rheumatology and Inflammation Research, Institute of Medicine, University of Göteborg, Göteborg, Sweden.
- 773 0_
- $w MED00180950 $t PloS one $x 1932-6203 $g Roč. 10, č. 4 (2015), s. e0124777
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25894334 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20160408 $b ABA008
- 991 __
- $a 20160408112352 $b ABA008
- 999 __
- $a ok $b bmc $g 1113727 $s 934666
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 10 $c 4 $d e0124777 $e 20150420 $i 1932-6203 $m PLoS One $n PLoS One $x MED00180950
- LZP __
- $a Pubmed-20160408