کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1929104 | 1050444 | 2012 | 6 صفحه PDF | دانلود رایگان |

ZFAT, originally identified as a candidate susceptibility gene for autoimmune thyroid disease, has been reported to be involved in apoptosis, development and primitive hematopoiesis. Zfat is highly expressed in T- and B-cells in the lymphoid tissues, however, its physiological function in the immune system remains totally unknown. Here, we generated the T cell-specific Zfat-deficient mice and demonstrated that Zfat-deficiency leads to a remarkable reduction in the number of the peripheral T cells. Intriguingly, a reduced expression of IL-7Rα and the impaired responsiveness to IL-7 for the survival were observed in the Zfat-deficient T cells. Furthermore, a severe defect in proliferation and increased apoptosis in the Zfat-deficient T cells following T cell receptor (TCR) stimulation was observed with a reduced IL-2Rα expression as well as a reduced IL-2 production. Thus, our findings reveal that Zfat is a critical regulator in peripheral T cell homeostasis and its TCR-mediated response.
► We generated Cd4-Cre-mediated T cell-specific Zfat-deficient mice.
► Zfat-deficiency leads to reduction in the number of the peripheral T cells.
► Impaired T cell receptor-mediated response in Zfat-deficient peripheral T cells.
► Decreased expression of IL-7Rα, IL-2Rα and IL-2 in Zfat-deficient peripheral T cells.
► Zfat plays critical roles in peripheral T cell homeostasis.
Journal: Biochemical and Biophysical Research Communications - Volume 425, Issue 1, 17 August 2012, Pages 107–112