Effects of Demethylation on the Expression of Foxp3 in T-reg Cells | An investigation on how epigenetic regulation of Foxp3 may influence the stability of regulatory T cell function

Edmund Yao

ISBN 10: 3659495093 / ISBN 13: 9783659495090

Published by LAP LAMBERT Academic Publishing, 2014

About this Item

Effects of Demethylation on the Expression of Foxp3 in T-reg Cells | An investigation on how epigenetic regulation of Foxp3 may influence the stability of regulatory T cell function | Edmund Yao | Taschenbuch | 92 S. | Englisch | 2014 | LAP LAMBERT Academic Publishing | EAN 9783659495090 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.

Seller Inventory # 105457019

Bibliographic Details

• Title: Effects of Demethylation on the Expression of Foxp3 in T-reg Cells | An investigation on how epigenetic regulation of Foxp3 may influence the stability of regulatory T cell function
• Publisher: LAP LAMBERT Academic Publishing
• Publication Date: 2014
• Language: English
• ISBN 10: 3659495093
• ISBN 13: 9783659495090
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 220W x 150H x 7D millimeters 220 millimeters width by 150 millimeters height by 7 millimeters depth
• Weight: 155 grams
• Seller catalogs:
  • Bücher

About this title

Synopsis

CD4+Foxp3+ regulatory T cells (TREG) are pivotal in the maintenance of immune tolerance to self-antigens and act as regulators of autoimmune reactions. There are two subsets of TREG: naturally occurring (nTREG) which develop in the thymus and inducible (iTREG) which are generated from conventional Foxp3- effector T cells (TCONV) in the periphery or in vitro. While both subsets require Foxp3 expression to function, iTREG cells gradually downregulate Foxp3 in vitro and lose their suppressive capabilities. In contrast, nTREG cells show constitutive Foxp3 expression and demonstrate stable suppressive function in vitro. Recent studies reveal a region of the Foxp3 locus that is differentially methylated between nTREG and iTREG. The methylation-sensitive region, known as the TREG-specific demethylated region (TSDR), is completely unmethylated in nTREG, partially methylated in iTREG, and heavily methylated in TCONV, suggesting that differential methylation patterns of the TSDR may account for unstable Foxp3 expression in iTREG. In this study, we investigate whether inhibition of DNMTs and thus methylation, impacts the stability of Foxp3 expression in cultured iTREG.

About the Author

Edmund Yao obtained his B.Sc. and M.Sc. in Immunology at McGill University under the supervision of Dr. Ciriaco Piccirillo. Initially drawn towards the field of immunology because of his food allergy to milk, Edmund now focusses on regulatory CD4+ T cells as his primary area of study.