The thymus is an organ in which T cells develop and their antigen recognition repertoire is established. 1 In the three-dimensional microenvironment composed of thymic stromal cells, immature T cells (called thymocytes) undergo stepwise developmental processes, including differentiation, proliferation, and cell fate determination in order to give rise to mature T cells expressing a diverse T cell receptor (TCR) repertoire. 2 The thymus parenchyma is subdivided into two regions, the cortex and medulla, wherein distinct subsets of thymic epithelial cells (TECs) form a reticular meshwork that houses developing thymocytes. 3,4 The cortex is the outer region with cortical TECs (cTECs) and thymocytes of immature stages, while the medulla is the inner region and is characterized by medullary TECs (mTECs) and mature thymocytes (Figure 1A). TECs play an essential role in T cell development, providing various signals in support of the survival, proliferation, migration, differentiation, and repertoire selection of thymocytes.Early T-cell progenitors (ETPs) from the fetal liver or adult bone marrow differentiate into CD4 − CD8 − (double negative, DN) thymocytes in the thymic cortex. Guided by cTECs, DN thymocytes are committed to the T-cell lineage and undergo rearrangements of the genes encoding the TCR. [3][4][5] In the adult thymus, ETPs arrive at the cortico-medullary junction (CMJ) where blood vessels are enriched, and developing DN thymocytes migrate through the cortex toward