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

Mediators Inflamm. 2016:2016:6985903. doi: 10.1155/2016/6985903. Epub 2016 May 11.

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, 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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • CD11b Antigen / genetics
  • Calcium Channels, L-Type / genetics
  • Caspase 1 / genetics
  • Child
  • Child, Preschool
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / genetics
  • Down Syndrome / genetics*
  • Down Syndrome / immunology
  • Female
  • Gene Expression Profiling
  • Group II Phospholipases A2 / genetics
  • Group V Phospholipases A2 / genetics
  • Humans
  • Inflammation / genetics*
  • Inflammation / immunology
  • Intercellular Adhesion Molecule-1 / genetics
  • Intracellular Signaling Peptides and Proteins / genetics
  • Male
  • Membrane Proteins / genetics
  • Phospholipase C beta / genetics
  • Phospholipase C delta / genetics
  • Real-Time Polymerase Chain Reaction
  • Receptors, Adrenergic, beta-1 / genetics
  • Receptors, Adrenergic, beta-2 / genetics
  • Receptors, Serotonin, 5-HT3 / genetics
  • Receptors, Tumor Necrosis Factor, Type II / genetics
  • Recombinant Fusion Proteins / genetics
  • Vascular Cell Adhesion Molecule-1 / genetics

Substances

  • ADRB1 protein, human
  • ADRB2 protein, human
  • Adaptor Proteins, Signal Transducing
  • CACNA1D protein, human
  • CD11b Antigen
  • CD40Ig protein, recombinant
  • Calcium Channels, L-Type
  • HTR3A protein, human
  • ICAM1 protein, human
  • ITGAM protein, human
  • ITGB1BP1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Receptors, Adrenergic, beta-1
  • Receptors, Adrenergic, beta-2
  • Receptors, Serotonin, 5-HT3
  • Receptors, Tumor Necrosis Factor, Type II
  • Recombinant Fusion Proteins
  • TNFRSF1B protein, human
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1
  • Group II Phospholipases A2
  • Group V Phospholipases A2
  • PLA2G2D protein, human
  • PLA2G5 protein, human
  • PLCB4 protein, human
  • PLCD1 protein, human
  • Phospholipase C beta
  • Phospholipase C delta
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • PDE4C protein, human
  • Caspase 1