Projects per year
The physiological role of the pro-survival BCL-2 family member A1 has been debated for a long time. Strong mRNA induction in T cells on T cell receptor (TCR)-engagement suggested a major role of A1 in the survival of activated T cells. However, the investigation of the physiological roles of A1 was complicated by the quadruplication of the A1 gene locus in mice, making A1 gene targeting very difficult. Here, we used the recently generated A1-/- mouse model to examine the role of A1 in T cell immunity. We confirmed rapid and strong induction of A1 protein in response to TCR/CD3 stimulation in CD4+ as well as CD8+ T cells. Surprisingly, on infection with the acute influenza HKx31 or the lymphocytic choriomeningitis virus docile strains mice lacking A1 did not show any impairment in the expansion, survival, or effector function of cytotoxic T cells. Furthermore, the ability of A1-/- mice to generate antigen-specific memory T cells or to provide adequate CD4-dependent help to B cells was not impaired. These results suggest functional redundancy of A1 with other pro-survival BCL-2 family members in the control of T cell-dependent immune responses.
|Number of pages||11|
|Journal||Cell Death and Differentiation|
|Publication status||Published - Mar 2017|
- 1 Finished
Apoptosis and stem cells in cancer development and therapy
Gerondakis, S., Adams, J. M., Bouillet, P., Colman, P., Cory, S., Huang, D., Kluck, R., Lindeman, G., Strasser, A., Vaux, D. & Visvader, J.
National Health and Medical Research Council (NHMRC) (Australia)
1/01/12 → 31/12/16