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Differential Expression of Inflammation-Related Genes in Children with Down Syndrome
Objective. The aim of the study was to investigate the expression patterns of a specific set of genes involved in the inflammation process in children with Down Syndrome (DS) and children without the syndrome (control group) to identify differences that may be related to the immune abnormalities obs...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879265/ https://www.ncbi.nlm.nih.gov/pubmed/27293319 http://dx.doi.org/10.1155/2016/6985903 |
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author | Silva, Cláudia Regina Santos Biselli-Périco, Joice Matos Zampieri, Bruna Lancia Silva, Wilson Araujo de Souza, Jorge Estefano Santana Bürger, Matheus Carvalho Goloni-Bertollo, Eny Maria Pavarino, Érika Cristina |
author_facet | Silva, Cláudia Regina Santos Biselli-Périco, Joice Matos Zampieri, Bruna Lancia Silva, Wilson Araujo de Souza, Jorge Estefano Santana Bürger, Matheus Carvalho Goloni-Bertollo, Eny Maria Pavarino, Érika Cristina |
author_sort | Silva, Cláudia Regina Santos |
collection | PubMed |
description | Objective. The aim of the study was to investigate the expression patterns of a specific set of genes involved in the inflammation process in children with Down Syndrome (DS) and children without the syndrome (control group) to identify differences that may be related to the immune abnormalities observed in DS individuals. Method. RNA samples were obtained from peripheral blood, and gene expression was quantified using the TaqMan® Array Plate Human Inflammation Kit, which facilitated the investigation into 92 inflammation-related genes and four reference genes using real-time polymerase chain reaction (qPCR). Results. Twenty genes showed differential expression in children with DS; 12 were overexpressed (PLA2G2D, CACNA1D, ALOX12, VCAM1, ICAM1, PLCD1, ADRB1, HTR3A, PDE4C, CASP1, PLA2G5, and PLCB4), and eight were underexpressed (LTA4H, BDKRB1, ADRB2, CD40LG, ITGAM, TNFRSF1B, ITGB1, and TBXAS1). After statistically correcting for the false discovery rate, only the genes BDKRB1 and LTA4H showed differential expression, and both were underexpressed within the DS group. Conclusion. DS children showed differential expression of inflammation-related genes that were not located on chromosome 21 compared with children without DS. The BDKRB1 and LTA4H genes may differentiate the case and control groups based on the inflammatory response, which plays an important role in DS pathogenesis. |
format | Online Article Text |
id | pubmed-4879265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-48792652016-06-12 Differential Expression of Inflammation-Related Genes in Children with Down Syndrome Silva, Cláudia Regina Santos Biselli-Périco, Joice Matos Zampieri, Bruna Lancia Silva, Wilson Araujo de Souza, Jorge Estefano Santana Bürger, Matheus Carvalho Goloni-Bertollo, Eny Maria Pavarino, Érika Cristina Mediators Inflamm Research Article Objective. The aim of the study was to investigate the expression patterns of a specific set of genes involved in the inflammation process in children with Down Syndrome (DS) and children without the syndrome (control group) to identify differences that may be related to the immune abnormalities observed in DS individuals. Method. RNA samples were obtained from peripheral blood, and gene expression was quantified using the TaqMan® Array Plate Human Inflammation Kit, which facilitated the investigation into 92 inflammation-related genes and four reference genes using real-time polymerase chain reaction (qPCR). Results. Twenty genes showed differential expression in children with DS; 12 were overexpressed (PLA2G2D, CACNA1D, ALOX12, VCAM1, ICAM1, PLCD1, ADRB1, HTR3A, PDE4C, CASP1, PLA2G5, and PLCB4), and eight were underexpressed (LTA4H, BDKRB1, ADRB2, CD40LG, ITGAM, TNFRSF1B, ITGB1, and TBXAS1). After statistically correcting for the false discovery rate, only the genes BDKRB1 and LTA4H showed differential expression, and both were underexpressed within the DS group. Conclusion. DS children showed differential expression of inflammation-related genes that were not located on chromosome 21 compared with children without DS. The BDKRB1 and LTA4H genes may differentiate the case and control groups based on the inflammatory response, which plays an important role in DS pathogenesis. Hindawi Publishing Corporation 2016 2016-05-11 /pmc/articles/PMC4879265/ /pubmed/27293319 http://dx.doi.org/10.1155/2016/6985903 Text en Copyright © 2016 Cláudia Regina Santos Silva et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Silva, Cláudia Regina Santos Biselli-Périco, Joice Matos Zampieri, Bruna Lancia Silva, Wilson Araujo de Souza, Jorge Estefano Santana Bürger, Matheus Carvalho Goloni-Bertollo, Eny Maria Pavarino, Érika Cristina Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title | Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title_full | Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title_fullStr | Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title_full_unstemmed | Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title_short | Differential Expression of Inflammation-Related Genes in Children with Down Syndrome |
title_sort | differential expression of inflammation-related genes in children with down syndrome |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879265/ https://www.ncbi.nlm.nih.gov/pubmed/27293319 http://dx.doi.org/10.1155/2016/6985903 |
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