Differential Expression of Inflammation-Related Genes in Children with Down Syndrome

Author:

Silva Cláudia Regina Santos1,Biselli-Périco Joice Matos1,Zampieri Bruna Lancia1,Silva Wilson Araujo234,de Souza Jorge Estefano Santana56,Bürger Matheus Carvalho5,Goloni-Bertollo Eny Maria1,Pavarino Érika Cristina1

Affiliation:

1. Unit of Research in Genetics and Molecular Biology (UPGEM), Department of Molecular Biology, Medical School of São José do Rio Preto (FAMERP), 15090-000 São José do Rio Preto, SP, Brazil

2. Department of Genetics, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, SP, Brazil

3. Center for Medical Genomics at HCFMRP/USP, Ribeirão Preto, SP, Brazil

4. Regional Blood of Ribeirão Preto at HCFMRP/USP, Ribeirão Preto, SP, Brazil

5. Institute of Bioinformatics and Biotechnology (2bio), Ribeirão Preto, SP, Brazil

6. Metrópole Digital Institute (IMD), UFRN, Natal, RN, Brazil

Abstract

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,andPLCB4), and eight were underexpressed (LTA4H,BDKRB1,ADRB2,CD40LG,ITGAM,TNFRSF1B,ITGB1,andTBXAS1). After statistically correcting for the false discovery rate, only the genesBDKRB1andLTA4Hshowed 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. TheBDKRB1andLTA4Hgenes may differentiate the case and control groups based on the inflammatory response, which plays an important role in DS pathogenesis.

Funder

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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