Abstract
The thymus is central to the establishment of a functioning immune system. Here is the place where T cells mature from hematopoietic progenitors, driven by mutual interactions of stromal cells and the developing thymocytes. As a result, different types of T cells are generated, all of which have been carefully selected for the ability to act in host defense towards non-self and against the potential to mount pathogenic self-reactive autoimmune responses. In this review we summarize our present knowledge on the lineage decisions taking place during this development, the selection processes responsible for shaping the T cell antigen-receptor repertoire, the interactions with the stromal components and the signal transduction pathways which transform the interactions with the thymic microenvironment into cellular responses of survival, proliferation, differentiation and, importantly, also of cell death.
MeSH Terms
Adaptor Proteins, Signal Transducing
Animals
Antigens, CD/metabolism
Carrier Proteins/metabolism
Cell Differentiation/physiology
Cell Lineage
Glucocorticoids/metabolism
Hematopoietic Stem Cells/physiology
Membrane Proteins/metabolism
Mitogen-Activated Protein Kinases/metabolism
Receptors, Antigen, T-Cell/metabolism
Receptors, Notch
Signal Transduction/physiology
T-Lymphocytes/physiology
Thymus Gland/cytology,physiology
Chemicals
Adaptor Proteins, Signal Transducing
Antigens, CD
Carrier Proteins
Glucocorticoids
Membrane Proteins
Receptors, Antigen, T-Cell
Receptors, Notch
Sh2d2a protein, mouse
Mitogen-Activated Protein Kinases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bommhardt U
Institute of Virology and Immunobiology, University of Würzburg, Versbacher Strasse 7, 97078 Würzburg, Germany.
Beyer M
Hünig T
Reichardt H M
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