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E-GEOD-23910 - AIRE hypoexpression and transcriptome profiles correlate with thymic impairment in Down syndrome

Status
Released on 28 November 2011, last updated on 26 June 2012
Organism
Homo sapiens
Samples (8)
Array (1)
Protocols (6)
Description
Down syndrome (DS) patients frequently develop organ-specific autoimmune disorders, particularly endocrinopathies and coeliac disease, as well as an increased susceptibility to mucosal candidiasis. These clinical features resemble APECED (autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy), a monogenic condition due to mutations in the AIRE gene, located on 21q22.3 and already described as down-regulated in 21 trisomy. Here we investigated AIRE expression and global gene expression profiles in surgically removed thymuses from 14 DS infants and children with congenital heart defects and from 42 age-matched individuals with cardiac defect as an isolated malformation. Immunohistochemistry revealed significantly reduced AIRE expression in DS thymuses (70.48±49.59 positive cells/mm2 in DS X 154.70±61.16 in controls, p<0.0001). qPCR confirmed the lower expression of AIRE in DS thymuses. Global thymic RNA profiles from DS patients and controls revealed 407 genes significantly hypoexpressed in DS. Network transcriptional analysis showed that hypoexpressed genes are related to biological processes such as antigen processing and presentation of endogenous antigen (ERAP2, CD1D), negative (PRDX2) and positive (CD3D, CD74) thymic T-cell selection and homeostasis of number of cells (PRDX2). Altogether these findings may explain the high prevalence of autoimmune phenomena in DS patients. Moreover, our data are in accordance with previous findings of thymic abnormal development in DS patients, characterized by lymphocyte depletion, diminution of the cortex, and loss of corticomedullary demarcation. Global gene profiles indicate that in DS patients, the trisomic imbalance probably leads to thymic hypofunction. In conclusion, lower AIRE expression and the impairment of other crucial pathways for central tolerance could well explain the high prevalence of organ-specific autoimmune disorders in DS. Among the 14 DS infants and 42 age-matched individuals with cardiac defect, only 4 from each group provided enough biological material (thymus fragments) for isolation of high-quality RNA to perform array analysis. Eight thymic samples were analyzed: C1, C2, C3 and C4 are controls, and D1, D2, D3 and D4 are from patients with Down syndrome.
Experiment type
transcription profiling by array 
Contacts
Patricia Locosque Ramos <locosque@usp.br>, Antonio Coutinho, Beatriz A Aguiar, Carlos A Moreira-Filho, Flavia A Lima, Helena Brentani, Leandro A Lima, Luciana B Souza, Luiz B Souza, Magaly Arrais, Magda Carneiro-Sampaio, Maria S Duarte, Patricia L Ramos
Citation
Decreased AIRE expression and global thymic hypofunction in Down syndrome. Lima FA, Moreira-Filho CA, Ramos PL, Brentani H, Lima Lde A, Arrais M, Bento-de-Souza LC, Bento-de-Souza L, Duarte MI, Coutinho A, Carneiro-Sampaio M. , PMID:21856934
MIAME
PlatformsProtocolsVariablesProcessedRaw
Files
Investigation descriptionE-GEOD-23910.idf.txt
Sample and data relationshipE-GEOD-23910.sdrf.txt
Raw data (1)E-GEOD-23910.raw.1.zip
Processed data (1)E-GEOD-23910.processed.1.zip
Array designA-AGIL-28.adf.txt
Links