دورية أكاديمية

Molecules that inhibit T-cell functions: cytochemical localization and shuttling

التفاصيل البيبلوغرافية
العنوان: Molecules that inhibit T-cell functions: cytochemical localization and shuttling
المؤلفون: CE Grossi, E Ciccone, D Zarcone, C Tacchetti, C Puri, D Saverino, G Anastasi, G Santoro
المصدر: European Journal of Histochemistry, Vol 44, Iss 1, Pp 89-100 (2009)
بيانات النشر: PAGEPress Publications, 2009.
سنة النشر: 2009
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: Biology (General), QH301-705.5
الوصف: Adaptive immune responses to antigens are mediated by specific receptors expressed on B cells (BCR’s) and T cells (TCR’s). Effector cells and memory cells are produced following a proliferative wave that accounts for clonal expansion. If not down-regulated, clonal expansion might lead to uncontrolled lymphoproliferation that would be harmful for the organism. Several mechanisms that account for the down-sizing of activated lymphocyte clones are briefly reviewed here. We next consider in detail one such mechanism that deals with the functional characterization and the immunocytochemical localization of two T-cell inhibitory molecules, namely the Cytotoxic T Lymphocyte Antigen-4 (CTLA-4) and the HP-F1 antigen, both present in all T lymphocytes . CTLA-4 and HP-F1 inhibit CD4+ T-helper cell proliferation and the lytic ability of CD8+ T-cytotoxic cells in non-specific and in antigen-specific cytolytic assays. Interestingly, a clonal distribution exists as for the ability of CTLA-4 and HP-F1 to inhibit T-cell functions. In resting and activated T cells, both molecules are largely confined in the endosomal compartment, as shown by immunofluorescence analyses. However, upon interaction of T cells with Antigen-Presenting Cells (APC’s) or with target cells that must be killed, CTLA-4 molecules are transported to the plasma membrane, at the site of cell-to-cell contact where, following interaction with ligands, they trigger inhibitory signals.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1121-760X
2038-8306
Relation: http://ejh.pagepress.org/index.php/ejh/article/view/1583; https://doaj.org/toc/1121-760X; https://doaj.org/toc/2038-8306
DOI: 10.4081/ejh.2000.89
URL الوصول: https://doaj.org/article/85f809abbe5e455b9dfe71e3dac91c4e
رقم الأكسشن: edsdoj.85f809abbe5e455b9dfe71e3dac91c4e
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1121760X
20388306
DOI:10.4081/ejh.2000.89