Intrathymic Expression of Genes Involved in Organ Specific Autoimmune Disease
Insulin, thyroglobulin and myelin basic protein (MBP) are implicated as autoantigens in the autoimmune diseases, insulin-dependent diabetes mellitus (IDDM), autoimmune thyroid-disease and multiple sclerosis. Self tolerance to these antigens, until recently only thought to be present extrathymically,...
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Published in: | Journal of autoimmunity Vol. 11; no. 4; pp. 309 - 318 |
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Format: | Journal Article |
Language: | English |
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01-08-1998
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Abstract | Insulin, thyroglobulin and myelin basic protein (MBP) are implicated as autoantigens in the autoimmune diseases, insulin-dependent diabetes mellitus (IDDM), autoimmune thyroid-disease and multiple sclerosis. Self tolerance to these antigens, until recently only thought to be present extrathymically, is generally considered to be maintained by ‘peripheral’ mechanisms, such as clonal anergy or clonal ignorance. The techniques of reverse transcription and polymerase chain reaction (RT-PCR) were used to investigate the intrathymic expression of these genes. Expression was examined in mRNA isolated from complete adult rat thymus, various mouse thymic cell-types isolated from fetal thymic-organ cultures and from neonatal-mouse thymocyte subsets. mRNA for insulin, thyroglobulin and MBP were detected in unfractionated adult rat and embryonic mouse thymus. Rat thymus expressed both insulin I and II, while mouse thymus only expressed insulin II. Thyroglobulin and MBP, but not insulin mRNA were detected in mouse MHC class II+thymic epthelial cells and class II+dendritic cells and in certain thymocyte subsets. The presence of insulin, thyroglobubin and MBP mRNA in the thymus has important implications for the development of the T-cell repertoire, particularly for the mechanisms of tolerance that prevent autoreactivity to these antigens in healthy individuals. |
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AbstractList | Insulin, thyroglobulin and myelin basic protein (MBP) are implicated as autoantigens in the autoimmune diseases, insulin-dependent diabetes mellitus (IDDM), autoimmune thyroid-disease and multiple sclerosis. Self tolerance to these antigens, until recently only thought to be present extrathymically, is generally considered to be maintained by ‘peripheral’ mechanisms, such as clonal anergy or clonal ignorance. The techniques of reverse transcription and polymerase chain reaction (RT-PCR) were used to investigate the intrathymic expression of these genes. Expression was examined in mRNA isolated from complete adult rat thymus, various mouse thymic cell-types isolated from fetal thymic-organ cultures and from neonatal-mouse thymocyte subsets. mRNA for insulin, thyroglobulin and MBP were detected in unfractionated adult rat and embryonic mouse thymus. Rat thymus expressed both insulin I and II, while mouse thymus only expressed insulin II. Thyroglobulin and MBP, but not insulin mRNA were detected in mouse MHC class II+thymic epthelial cells and class II+dendritic cells and in certain thymocyte subsets. The presence of insulin, thyroglobubin and MBP mRNA in the thymus has important implications for the development of the T-cell repertoire, particularly for the mechanisms of tolerance that prevent autoreactivity to these antigens in healthy individuals. Insulin, thyroglobulin and myelin basic protein (MBP) are implicated as autoantigens in the autoimmune diseases, insulin-dependent diabetes mellitus (IDDM), autoimmune thyroid-disease and multiple sclerosis. Self tolerance to these antigens, until recently only thought to be present extrathymically, is generally considered to be maintained by 'peripheral' mechanisms, such as clonal anergy or clonal ignorance. The techniques of reverse transcription and polymerase chain reaction (RT-PCR) were used to investigate the intrathymic expression of these genes. Expression was examined in mRNA isolated from complete adult rat thymus, various mouse thymic cell-types isolated from fetal thymic-organ cultures and from neonatal-mouse thymocyte subsets. mRNA for insulin, thyroglobulin and MBP were detected in unfractionated adult rat and embryonic mouse thymus. Rat thymus expressed both insulin I and II, while mouse thymus only expressed insulin II. Thyroglobulin and MBP, but not insulin mRNA were detected in mouse MHC class II super(+) thymic epithelial cells and class II super(+) dendritic cells and in certain thymocyte subsets. The presence of insulin, thyroglobubin and MBP mRNA in the thymus has important implications for the development of the T-cell repertoire, particularly for the mechanisms of tolerance that prevent autoreactivity to these antigens in healthy individuals. |
Author | Mason, Don W Heath, Victoria L Moore, Nel C Parnell, Sonia M |
Author_xml | – sequence: 1 givenname: Victoria L surname: Heath fullname: Heath, Victoria L organization: The Cellular Immunology Unit, Sir William Dunn School of Pathology, Oxford, OX1 3RE, UK – sequence: 2 givenname: Nel C surname: Moore fullname: Moore, Nel C organization: CCRIS, The Medical School, University of Birmingham, Birmingham, B15 2TT, UK – sequence: 3 givenname: Sonia M surname: Parnell fullname: Parnell, Sonia M organization: CCRIS, The Medical School, University of Birmingham, Birmingham, B15 2TT, UK – sequence: 4 givenname: Don W surname: Mason fullname: Mason, Don W organization: The Cellular Immunology Unit, Sir William Dunn School of Pathology, Oxford, OX1 3RE, UK |
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ContentType | Journal Article |
Copyright | 1998 Academic Press 1998 INIST-CNRS Copyright 1998 Academic Press |
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Keywords | thymus central tolerance myelin basic protein insulin thyroglobulin Endocrinopathy Human Thyroiditis Immunopathology Nervous system diseases Multiple sclerosis Thymus gland Thyroid diseases Exploration Autoimmune disease Gene expression Inflammatory disease Autoantigen Messenger RNA Central nervous system disease Insulin dependent diabetes Molecular biology |
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SubjectTerms | Animals Autoantigens - genetics Autoantigens - immunology Autoimmune Diseases - genetics Autoimmune Diseases - metabolism Biological and medical sciences central tolerance DNA, Complementary - genetics DNA, Complementary - metabolism General aspects Immunopathology insulin Insulin - biosynthesis Insulin - genetics Male Medical sciences Mice myelin basic protein Myelin Basic Protein - biosynthesis Myelin Basic Protein - genetics Organ Culture Techniques Organ Specificity Rats Rats, Inbred Strains Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - metabolism thymus Thymus Gland - immunology Thymus Gland - metabolism thyroglobulin Thyroglobulin - biosynthesis Thyroglobulin - genetics |
Title | Intrathymic Expression of Genes Involved in Organ Specific Autoimmune Disease |
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