| First Author | Klibi J | Year | 2020 |
| Journal | Front Immunol | Volume | 11 |
| Pages | 815 | PubMed ID | 32457751 |
| Mgi Jnum | J:312577 | Mgi Id | MGI:6728957 |
| Doi | 10.3389/fimmu.2020.00815 | Citation | Klibi J, et al. (2020) Cortical Thymocytes Along With Their Selecting Ligands Are Required for the Further Thymic Maturation of NKT Cells in Mice. Front Immunol 11:815 |
| abstractText | Following positive selection, NKT cell precursors enter an "NK-like" program and progress from an NK(-) to an NK(+) maturational stage to give rise to NKT1 cells. Maturation takes place in the thymus or after emigration of NK(-) NKT cells to the periphery. In this study, we followed the fate of injected NKT cells at the NK(-) stage of their development in the thymus of a series of mice with differential CD1d expression. Our results indicate that CD1d-expressing cortical thymocytes, and not epithelial cells, macrophages, or dendritic cells, are necessary and sufficient to promote the maturation of thymic NKT1 cells. Migration out of the thymus of NK(-) NKT cells occurred in the absence of CD1d expression, however, CD1d expression is required for maturation in peripheral organs. We also found that the natural ligand Isoglobotriosylceramide (iGb3), and the cysteine protease Cathepsin L, both localizing with CD1d in the endosomal compartment and crucial for NKT cell positive selection, are also required for NK(-) to NK(+) NKT cell transition. Overall, our study indicates that the maturational transition of NKT cells require continuous TCR/CD1d interactions and suggest that these interactions occur in the thymic cortex where DP cortical thymocytes are located. We thus concluded that key components necessary for positive selection of NKT cells are also required for subsequent maturation. |
