Subcellular Location and Expression Pattern of Autoimmune Regulator (Aire), the Mouse Orthologue for Human Gene Defective in Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED)
Субклеточная локализация и характер экспрессии аутоиммунного регулятора (Aire) — мышиного ортолога человеческого гена, дефектного при аутоиммунном полиэндокринном кандидозе и эктодермальной дистрофии (APECED)
2001-02-01
SCID: 54.1/urt6mvpz
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APECEDAutoimmune polyendocrinopathyAutoimmune regulator (Aire)Mouse tissuesSubcellular localization
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Abstract (AI)
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED), also known as autoimmune polyglandular syndrome Type I (APS1), is an autosomal recessive autoimmune disease caused by mutations in a gene designated as AIRE (autoimmune regulator). Here we have studied the expression of Aire in transfected cell lines and in adult mouse tissues. Our results show that Aire has a dual subcellular location and that it is expressed in multiple immunologically relevant tissues such as the thymus, spleen, lymph nodes, and bone marrow. In addition, Aire expression was detected in various other tissues such as kidney, testis, adrenal glands, liver, and ovary. These findings suggest that APECED protein might also have a function(s) outside the immune system.(J Histochem Cytochem 49:197-208, 2001)
Key Findings
1
Aire exhibits a dual subcellular localization in transfected cell lines.
2
Aire expression is also detected in kidney, testis, adrenal glands, liver, and ovary.
3
Aire is expressed in multiple immunologically relevant mouse tissues, including thymus, spleen, lymph nodes, and bone marrow.
4
Aire’s broad tissue distribution suggests that the APECED protein may have functions beyond the immune system.
Research Object
Aire (autoimmune regulator) in transfected cell lines and adult mouse tissues
Research Subject
Aire subcellular localization and tissue-specific expression pattern, including its distribution in immunologically relevant and nonimmune tissues
Publication Details
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2001-02-01
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