Transcriptional regulation of T cell tolerance

التفاصيل البيبلوغرافية
العنوان: Transcriptional regulation of T cell tolerance
المؤلفون: Noemi Soto-Nieves, Sanmay Bandyopadhyay, Fernando Macian
المصدر: The Epigenetics of Autoimmune Diseases
بيانات النشر: Elsevier BV, 2007.
سنة النشر: 2007
مصطلحات موضوعية: Clonal Anergy, Transcription, Genetic, Clonal anergy, T-Lymphocytes, ZAP70, T cell, Immunology, Peripheral tolerance, CD28, Biology, Article, Cell biology, Interleukin 21, medicine.anatomical_structure, Gene Expression Regulation, Immune Tolerance, medicine, Animals, Humans, Immunology and Allergy, Cytotoxic T cell, IL-2 receptor
الوصف: Self-reactive T cells that escape negative selection in the thymus must be kept under control in the periphery. Mechanisms of peripheral tolerance include deletion or functional inactivation of self-reactive T cells and mechanisms of dominant tolerance mediated by regulatory T cells. In the absence of costimulation, T cell receptor (TCR) engagement results in unopposed calcium signaling that leads to the activation of a cell-intrinsic program of inactivation, which makes T cells hyporesponsive to subsequent stimulations. The activation of this program in anergic T cells is a consequence of the induction of a nuclear factor of activated T cells (NFAT)-dependent program of gene expression. Recent studies have offered new insights into the mechanisms responsible for the implementation and maintenance of T cell anergy and have provided evidence that the proteins encoded by the genes upregulated in anergic T cells are responsible for the implementation of anergy by interfering with TCR signaling or directly inhibiting cytokine gene transcription.
تدمد: 1044-5323
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d5a4509b259908d7a7911b4539757cdTest
https://doi.org/10.1016/j.smim.2007.02.006Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....2d5a4509b259908d7a7911b4539757cd
قاعدة البيانات: OpenAIRE
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