suck pdf from google scholar
unlimited free pdf from europmc19641188    free
PDF from PMC    free
html from PMC    free
PDF vom PMID19641188  :  Publisher
suck pdf from library genesis
English Wikipedia

Nephropedia Template TP (

Twit Text

  • DeepDyve
  • Pubget Overpricing

  • lüll
  • Epigenetic mechanisms of regulation of Foxp3 expression
  • Lal G; Bromberg JS
  • Blood 2009[Oct]; 114 (18): 3727-35
  • Regulatory T cells play important roles in the control of autoimmunity and maintenance of transplantation tolerance. Foxp3, a member of the forkhead/winged-helix family of transcription factors, acts as the master regulator for regulatory T-cell (Treg) development and function. Mutation of the Foxp3 gene causes the scurfy phenotype in mouse and IPEX syndrome (immune dysfunction, polyendocrinopathy, enteropathy, X-linked syndrome) in humans. Epigenetics is defined by regulation of gene expression without altering nucleotide sequence in the genome. Several epigenetic markers, such as histone acetylation and methylation, and cytosine residue methylation in CpG dinucleotides, have been reported at the Foxp3 locus. In particular, CpG dinucleotides at the Foxp3 locus are methylated in naive CD4+CD25- T cells, activated CD4+ T cells, and TGF-beta-induced adaptive Tregs, whereas they are completely demethylated in natural Tregs. The DNA methyltransferases DNMT1 and DNMT3b are associated with the Foxp3 locus in CD4+ T cells. Methylation of CpG residues represses Foxp3 expression, whereas complete demethylation is required for stable Foxp3 expression. In this review, we discuss how different cis-regulatory elements at the Foxp3 locus are subjected to epigenetic modification in different subsets of CD4+ T cells and regulate Foxp3 expression, and how these mechanisms can be exploited to generate efficiently large numbers of suppressive Tregs for therapeutic purposes.
  • |*Epigenesis, Genetic[MESH]
  • |Animals[MESH]
  • |Autoimmunity/genetics[MESH]
  • |CpG Islands/genetics/immunology[MESH]
  • |DNA (Cytosine-5-)-Methyltransferase 1[MESH]
  • |DNA (Cytosine-5-)-Methyltransferases/genetics/immunology/metabolism[MESH]
  • |DNA Methylation/genetics/immunology[MESH]
  • |Forkhead Transcription Factors/*biosynthesis/genetics/immunology[MESH]
  • |Genetic Diseases, X-Linked/genetics/immunology/metabolism[MESH]
  • |Humans[MESH]
  • |Immune Tolerance/genetics[MESH]
  • |Lymphocyte Activation/genetics/immunology[MESH]
  • |Mice[MESH]
  • |Mutation[MESH]
  • |Polyendocrinopathies, Autoimmune/genetics/immunology/metabolism[MESH]
  • |T-Lymphocyte Subsets/immunology/*metabolism[MESH]
  • |T-Lymphocytes, Regulatory/immunology/*metabolism[MESH]
  • |Transforming Growth Factor beta/genetics/immunology/metabolism[MESH]

  • *{{pmid19641188}}
    *<b>[ Epigenetic mechanisms of regulation of Foxp3 expression ]</b> Blood 2009; 114(18) ; 3727-35 Lal G; Bromberg JS


    Nephropedia PMID record

    Deutsche Wikipedia - im Artikel

    Hier den unten stehenden Textblock hineinkopieren


    3727 18.114 2009