| First Author | Zhu Y | Year | 2020 |
| Journal | Int Immunol | Volume | 32 |
| Issue | 5 | Pages | 307-319 |
| PubMed ID | 31875880 | Mgi Jnum | J:299923 |
| Mgi Id | MGI:6490828 | Doi | 10.1093/intimm/dxz082 |
| Citation | Zhu Y, et al. (2020) Intestinal epithelial cell-derived IL-15 determines local maintenance and maturation of intra-epithelial lymphocytes in the intestine. Int Immunol 32(5):307-319 |
| abstractText | Interleukin-15 (IL-15) is a cytokine critical for maintenance of intestinal intra-epithelial lymphocytes (IELs), especially CD8alphaalpha + IELs (CD8alphaalpha IELs). In the intestine, IL-15 is produced by intestinal epithelial cells (IECs), blood vascular endothelial cells (BECs) and hematopoietic cells. However, the precise role of intestinal IL-15 on IELs is still unknown. To address the question, we generated two kinds of IL-15 conditional knockout (IL-15cKO) mice: villin-Cre (Vil-Cre) and Tie2-Cre IL-15cKO mice. IEC-derived IL-15 was specifically deleted in Vil-Cre IL-15cKO mice, whereas IL-15 produced by BECs and hematopoietic cells was deleted in Tie2-Cre IL-15cKO mice. The cell number and frequency of CD8alphaalpha IELs and NK IELs were significantly reduced in Vil-Cre IL-15cKO mice. By contrast, CD8alphaalpha IELs were unchanged in Tie2-Cre IL-15cKO mice, indicating that IL-15 produced by BECs and hematopoietic cells is dispensable for CD8alphaalpha IELs. Expression of an anti-apoptotic factor, Bcl-2, was decreased, whereas Fas expression was increased in CD8alphaalpha IELs of Vil-Cre IL-15cKO mice. Forced expression of Bcl-2 by a Bcl-2 transgene partially restored CD8alphaalpha IELs in Vil-Cre IL-15cKO mice, suggesting that some IL-15 signal other than Bcl-2 is required for maintenance of CD8alphaalpha IELs. Furthermore, granzyme B production was reduced, whereas PD-1 expression was increased in CD8alphaalpha IELs of Vil-Cre IL-15cKO mice. These results collectively suggested that IEC-derived IL-15 is essential for homeostasis of IELs by promoting their survival and functional maturation. |
