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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
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.
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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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