Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2004-5-18
pubmed:abstractText
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a systemic disease with autoimmune characteristics caused by mutations in a single gene called AIRE. Although a defect in negative selection has been emphasized for the pathogenesis of the autoimmune symptoms on the basis of studies of Aire-targeted mice, the function of the gene in the peripheral immune system and the cause of immunodeficiency noted in the disease have not been clarified yet. In this study, we demonstrated using murine Aire transfectants that Aire downregulates IL-1 receptor antagonist (IL-1Ra), which is important for immune suppression, and major histocompatibility complex (MHC) class II molecules, which are critical for acquired immunity. It was surprising to learn that Aire, which has been supposed to positively regulate transcription, downregulates multiple molecules. This downregulation of IL-1Ra and MHC class II molecules seems to be caused by the competition for transcriptional coactivator, CREB-binding protein (CBP), and may explain part of the contradictory (i.e., both autoimmune and immunodeficient) nature of APECED.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/APECED protein, http://linkedlifedata.com/resource/pubmed/chemical/CREB-Binding Protein, http://linkedlifedata.com/resource/pubmed/chemical/Crebbp protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II, http://linkedlifedata.com/resource/pubmed/chemical/Il1rn protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Immunologic Factors, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin 1 Receptor Antagonist..., http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Sialoglycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-291X
pubmed:author
pubmed:issnType
Print
pubmed:day
11
pubmed:volume
318
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
935-40
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:15147962-Animals, pubmed-meshheading:15147962-Base Sequence, pubmed-meshheading:15147962-CREB-Binding Protein, pubmed-meshheading:15147962-Cytokines, pubmed-meshheading:15147962-Down-Regulation, pubmed-meshheading:15147962-Histocompatibility Antigens Class II, pubmed-meshheading:15147962-Immunologic Factors, pubmed-meshheading:15147962-Interleukin 1 Receptor Antagonist Protein, pubmed-meshheading:15147962-Lipopolysaccharides, pubmed-meshheading:15147962-Mice, pubmed-meshheading:15147962-Molecular Sequence Data, pubmed-meshheading:15147962-Nuclear Proteins, pubmed-meshheading:15147962-Polyendocrinopathies, Autoimmune, pubmed-meshheading:15147962-Promoter Regions, Genetic, pubmed-meshheading:15147962-RNA, Messenger, pubmed-meshheading:15147962-Receptors, Interleukin-1, pubmed-meshheading:15147962-Recombinant Proteins, pubmed-meshheading:15147962-Sialoglycoproteins, pubmed-meshheading:15147962-Trans-Activators, pubmed-meshheading:15147962-Transcription Factors, pubmed-meshheading:15147962-Transfection
pubmed:year
2004
pubmed:articleTitle
Aire downregulates multiple molecules that have contradicting immune-enhancing and immune-suppressive functions.
pubmed:affiliation
Department of Allergy and Rheumatology, Graduate School of Medicine and Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-8655, Japan. satok.cell@tmd.ac.jp
pubmed:publicationType
Journal Article