Abstract
The population size of the T cells is tightly regulated. The T cell number drastically increases in response to their specific antigens. Upon antigen clearance, the T cell number decreases over time. Apoptosis, also called type I programmed cell death, plays an important role in eliminating T cells. The role of autophagic cell death, also called type II programmed cell death, is unclear in T cells. Our recent work demonstrated that autophagy is induced in both Th1 and Th2 cells. Both TCR signaling and IL-2 increase autophagy in T cells, and JNK MAP kinases are required for the induction of autophagy in T cells, whereas caspases and mTOR inhibit autophagy in T cells. Autophagy is required for mediating growth factor withdrawal-dependent cell death in T cells. Here, we hypothesize that autophagic cell death plays an important role in T cell homeostasis.
| Original language | English |
|---|---|
| Pages (from-to) | 158-159 |
| Number of pages | 2 |
| Journal | Autophagy |
| Volume | 3 |
| Issue number | 2 |
| DOIs | |
| State | Published - 2007 |
Keywords
- Apoptosis
- Autophagy
- Effector T cell
- Homeostasis
- Programmed cell death
- Th1
- Th2
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