Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice

<p>Abstract</p> <p>Scurfy mice display the most severe form of multi-organ inflammation due to total lack of the CD4<sup>+</sup>Foxp3<sup>+ </sup>regulatory T cells (Treg) resulted from a mutation of the X-linked transcription factor Foxp3. A large repertoir...

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Main Authors: Ju Shyr-Te, Fu Shu Man, Sung Sun-sang, Sharma Rahul
Format: Article
Language:English
Published: BMC 2009-02-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/16/1/20
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spelling doaj-a984c42f32a24458805ad0fcf8e598c92020-11-24T23:06:48ZengBMCJournal of Biomedical Science1021-77701423-01272009-02-011612010.1186/1423-0127-16-20Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy miceJu Shyr-TeFu Shu ManSung Sun-sangSharma Rahul<p>Abstract</p> <p>Scurfy mice display the most severe form of multi-organ inflammation due to total lack of the CD4<sup>+</sup>Foxp3<sup>+ </sup>regulatory T cells (Treg) resulted from a mutation of the X-linked transcription factor Foxp3. A large repertoire of Treg-suppressible, inflammation-inducing T cells was demonstrated by adoptive transfer experiments using <it>Rag1</it><sup>-/- </sup>mice as recipients and by prolongation of lifespan through breeding with <it>Fas</it><sup><it>lpr</it>/<it>lpr </it></sup>mutant. Inflammation in the ear, eyes, skin, tail, salivary glands, lungs, stomach, pancreas, liver, small intestine, colon, skeletal muscle, and accessory reproductive organs are identified. Genetic and cellular regulations of specific organ inflammation are described. Sf mice may be useful for the identification of organ-specific antigens and Treg capable of suppressing inflammation in an organ-specific manner. Sf mice are also useful to determine the important inflammation process at the checkpoint after Treg regulation using genetic analysis through breeding.</p> http://www.jbiomedsci.com/content/16/1/20
collection DOAJ
language English
format Article
sources DOAJ
author Ju Shyr-Te
Fu Shu Man
Sung Sun-sang
Sharma Rahul
spellingShingle Ju Shyr-Te
Fu Shu Man
Sung Sun-sang
Sharma Rahul
Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
Journal of Biomedical Science
author_facet Ju Shyr-Te
Fu Shu Man
Sung Sun-sang
Sharma Rahul
author_sort Ju Shyr-Te
title Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
title_short Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
title_full Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
title_fullStr Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
title_full_unstemmed Regulation of multi-organ inflammation in the regulatory T cell-deficient scurfy mice
title_sort regulation of multi-organ inflammation in the regulatory t cell-deficient scurfy mice
publisher BMC
series Journal of Biomedical Science
issn 1021-7770
1423-0127
publishDate 2009-02-01
description <p>Abstract</p> <p>Scurfy mice display the most severe form of multi-organ inflammation due to total lack of the CD4<sup>+</sup>Foxp3<sup>+ </sup>regulatory T cells (Treg) resulted from a mutation of the X-linked transcription factor Foxp3. A large repertoire of Treg-suppressible, inflammation-inducing T cells was demonstrated by adoptive transfer experiments using <it>Rag1</it><sup>-/- </sup>mice as recipients and by prolongation of lifespan through breeding with <it>Fas</it><sup><it>lpr</it>/<it>lpr </it></sup>mutant. Inflammation in the ear, eyes, skin, tail, salivary glands, lungs, stomach, pancreas, liver, small intestine, colon, skeletal muscle, and accessory reproductive organs are identified. Genetic and cellular regulations of specific organ inflammation are described. Sf mice may be useful for the identification of organ-specific antigens and Treg capable of suppressing inflammation in an organ-specific manner. Sf mice are also useful to determine the important inflammation process at the checkpoint after Treg regulation using genetic analysis through breeding.</p>
url http://www.jbiomedsci.com/content/16/1/20
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