Abstract
The mechanism of CD4-CD8 lineage commitment, which ensures the correlation between T cell receptor specificity and adoption of the T killer or T helper phenotype, has long been the subject of intense debate. Various approaches are slowly elucidating the underlying molecular pathways. Analysis of the function of T cell receptor signaling (the 'top-down' approach) supports the view that differences in signal strength and/or duration 'instruct' alternative commitment. Analysis of the transcriptional regulation of the genes encoding CD4 and CD8 (the 'bottom-up' approach) has identified critical cis-acting elements and their interacting factors. Finally, identification of the transcription factor Th-POK as a central component of the CD4 lineage - determining pathway has provided a new starting point from which to unravel this intriguing process 'from the inside out'.
Original language | English |
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Pages (from-to) | 761-767 |
Number of pages | 6 |
Journal | Nature Immunology |
Volume | 6 |
Issue number | 8 |
DOIs | |
State | Published - Aug 2005 |
Keywords
- Animals
- CD4-Positive T-Lymphocytes/cytology
- CD8-Positive T-Lymphocytes/cytology
- Cell Differentiation
- Cell Lineage
- Chromatin/metabolism
- Gene Silencing
- Humans
- Killer Cells, Natural/cytology
- Models, Biological
- Models, Immunological
- Phenotype
- Signal Transduction
- T-Lymphocytes, Helper-Inducer/cytology
- Transcription Factors/metabolism
- Transcription, Genetic