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Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens
BACKGROUND: Food allergy is a serious health concern among infants and young children. Although immunological mechanism of food allergy is well documented, the molecular mechanism(s) involved in food allergen sensitization have not been well characterized. Therefore, the present study analyzed the m...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023748/ https://www.ncbi.nlm.nih.gov/pubmed/21211037 http://dx.doi.org/10.1186/1471-2164-12-12 |
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author | Husain, Mainul Boermans, Herman J Karrow, Niel A |
author_facet | Husain, Mainul Boermans, Herman J Karrow, Niel A |
author_sort | Husain, Mainul |
collection | PubMed |
description | BACKGROUND: Food allergy is a serious health concern among infants and young children. Although immunological mechanism of food allergy is well documented, the molecular mechanism(s) involved in food allergen sensitization have not been well characterized. Therefore, the present study analyzed the mesenteric lymph node (MLN) transcriptome profiles of BALB/c mice in response to three common food allergens. RESULTS: Microarray analysis identified a total of 1361, 533 and 488 differentially expressed genes in response to β-lactoglobulin (BLG) from cow's milk, ovalbumin (OVA) from hen's egg white and peanut agglutinin (PNA) sensitizations, respectively (p < 0.05). A total of 150 genes were commonly expressed in all antigen sensitized groups. The expression of seven representative genes from microarray experiment was validated by real-time RT-PCR. All allergens induced significant ear swelling and serum IgG1 concentrations, whereas IgE concentrations were increased in BLG- and PNA-treated mice (p < 0.05). Treatment with OVA and PNA significantly induced plasma histamine concentrations (p < 0.05). The PCA demonstrated the presence of allergen-specific IgE in the serum of previously sensitized and challenged mice. CONCLUSIONS: Immunological profiles indicate that the allergen dosages used are sufficient to sensitize the BALB/c mice and to conduct transcriptome profiling. Microarray studies identified several differentially expressed genes in the sensitization phase of the food allergy. These findings will help to better understand the underlying molecular mechanism(s) of food allergen sensitizations and may be useful in identifying the potential biomarkers of food allergy. |
format | Text |
id | pubmed-3023748 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30237482011-01-20 Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens Husain, Mainul Boermans, Herman J Karrow, Niel A BMC Genomics Research Article BACKGROUND: Food allergy is a serious health concern among infants and young children. Although immunological mechanism of food allergy is well documented, the molecular mechanism(s) involved in food allergen sensitization have not been well characterized. Therefore, the present study analyzed the mesenteric lymph node (MLN) transcriptome profiles of BALB/c mice in response to three common food allergens. RESULTS: Microarray analysis identified a total of 1361, 533 and 488 differentially expressed genes in response to β-lactoglobulin (BLG) from cow's milk, ovalbumin (OVA) from hen's egg white and peanut agglutinin (PNA) sensitizations, respectively (p < 0.05). A total of 150 genes were commonly expressed in all antigen sensitized groups. The expression of seven representative genes from microarray experiment was validated by real-time RT-PCR. All allergens induced significant ear swelling and serum IgG1 concentrations, whereas IgE concentrations were increased in BLG- and PNA-treated mice (p < 0.05). Treatment with OVA and PNA significantly induced plasma histamine concentrations (p < 0.05). The PCA demonstrated the presence of allergen-specific IgE in the serum of previously sensitized and challenged mice. CONCLUSIONS: Immunological profiles indicate that the allergen dosages used are sufficient to sensitize the BALB/c mice and to conduct transcriptome profiling. Microarray studies identified several differentially expressed genes in the sensitization phase of the food allergy. These findings will help to better understand the underlying molecular mechanism(s) of food allergen sensitizations and may be useful in identifying the potential biomarkers of food allergy. BioMed Central 2011-01-06 /pmc/articles/PMC3023748/ /pubmed/21211037 http://dx.doi.org/10.1186/1471-2164-12-12 Text en Copyright ©2011 Husain et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Husain, Mainul Boermans, Herman J Karrow, Niel A Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title | Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title_full | Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title_fullStr | Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title_full_unstemmed | Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title_short | Mesenteric lymph node transcriptome profiles in BALB/c mice sensitized to three common food allergens |
title_sort | mesenteric lymph node transcriptome profiles in balb/c mice sensitized to three common food allergens |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3023748/ https://www.ncbi.nlm.nih.gov/pubmed/21211037 http://dx.doi.org/10.1186/1471-2164-12-12 |
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