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Creado por gina_evans0312
hace más de 12 años
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| Pregunta | Respuesta |
| T-Cells Before Development | Immature, 'double negative' cells |
| +ve Selection- Location | Done in the cortex of the thymus |
| +ve Selection- Role | Removal of weakly binding/non functional T-cells |
| +ve Selection- Thymic Epithelial Cells | Express both MCHI & MCHII, essentially functioning as antigen presenting cells |
| +ve Selection- TCR Binding | Binding causes the switching off of aptotic genes- T cells that can bind do not apoptose |
| +ve Selection- No TCR Binding | Aptotic genes remain functional and weakly/non binding cells apoptose |
| +ve Selection- T Cells After Selection | Immature 'double +ve' T cells that express both CD4 & CD8 |
| -ve Selection- Location | Corto-medullary junction |
| -ve Selection- Cells Used | Interdigitating Dendritic Cells |
| -ve Selection- Antigen Presentation | Interdigitating cells present self antigens to 'double positive' T cells |
| -ve Selection- Overly Strong Binding | T-cell is actively apoptosed to prevent auto-immune disorders |
| -ve Selection- Thymic Macrophages | Destroy T-cells that bind too strongly to the 'self' antigens |
| -ve Selection- Promiscuous Gene Expression | Allows thymic cells to present ALL antigens (even those on other organs or those only expressed at certain times) so the T cell can be tested against the whole body |
| -ve Selection- End Cells | 'Single +ve' cells that only express CD4 or CD8 |
| Creation of Single +ve Cells | Either double +ve cell binds to MCHI by chance and becomes CD4 (or vice versa) or randomly, TCR will upregulate production of one and downregulate other |
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