Source:http://linkedlifedata.com/resource/pubmed/id/17947713
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2007-10-19
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pubmed:abstractText |
Why systemic lupus erythematosus primarily affects women is unknown. Recent evidence indicates that human lupus is an epigenetic disease characterized by impaired T cell DNA methylation. Women have two X chromosomes; one is inactivated by mechanisms including DNA methylation. We hypothesized that demethylation of sequences on the inactive X may cause gene overexpression uniquely in women, predisposing them to lupus. We therefore compared expression and methylation of CD40LG, a B cell costimulatory molecule encoded on the X chromosome, in experimentally demethylated T cells from men and women and in men and women with lupus. Controls included TNFSF7, a methylation-sensitive autosomal B cell costimulatory molecule known to be demethylated and overexpressed in lupus. Bisulfite sequencing revealed that CD40LG is unmethylated in men, while women have one methylated and one unmethylated gene. 5-Azacytidine, a DNA methyltransferase inhibitor, demethylated CD40LG and doubled its expression on CD4(+) T cells from women but not men, while increasing TNFSF7 expression equally between sexes. Similar studies demonstrated that CD40LG demethylates in CD4(+) T cells from women with lupus, and that women but not men with lupus overexpress CD40LG on CD4(+) T cells, while both overexpress TNFSF7. These studies demonstrate that regulatory sequences on the inactive X chromosome demethylate in T cells from women with lupus, contributing to CD40LG overexpression uniquely in women. Demethylation of CD40LG and perhaps other genes on the inactive X may contribute to the striking female predilection of this disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD70,
http://linkedlifedata.com/resource/pubmed/chemical/CD40 Ligand,
http://linkedlifedata.com/resource/pubmed/chemical/CD70 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
179
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6352-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17947713-Adult,
pubmed-meshheading:17947713-Antigens, CD70,
pubmed-meshheading:17947713-CD40 Ligand,
pubmed-meshheading:17947713-DNA,
pubmed-meshheading:17947713-Female,
pubmed-meshheading:17947713-Gene Expression Regulation,
pubmed-meshheading:17947713-Humans,
pubmed-meshheading:17947713-Lupus Erythematosus, Systemic,
pubmed-meshheading:17947713-Male,
pubmed-meshheading:17947713-Methylation,
pubmed-meshheading:17947713-Middle Aged,
pubmed-meshheading:17947713-Promoter Regions, Genetic,
pubmed-meshheading:17947713-RNA, Messenger,
pubmed-meshheading:17947713-Sex Characteristics,
pubmed-meshheading:17947713-T-Lymphocytes,
pubmed-meshheading:17947713-X Chromosome Inactivation
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pubmed:year |
2007
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pubmed:articleTitle |
Demethylation of CD40LG on the inactive X in T cells from women with lupus.
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pubmed:affiliation |
Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, 41011 Hunan, China.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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