TY - JOUR
T1 - Notch activation in thymic epithelial cells induces development of thymic microenvironments
AU - Masuda, Kyoko
AU - Germeraad, Wilfred T.V.
AU - Satoh, Rumi
AU - Itoi, Manami
AU - Ikawa, Tomokatsu
AU - Minato, Nagahiro
AU - Katsura, Yoshimoto
AU - van Ewijk, Willem
AU - Kawamoto, Hiroshi
N1 - Funding Information:
This work was supported by the Special Coordination Funds for Promoting Science and Technology from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2009/5
Y1 - 2009/5
N2 - The development and maintenance of thymic microenvironments depends on sustained crosstalk signals derived from developing thymocytes. However, the molecular basis for the initial phase in the lymphoid dependent development of thymic epithelial cells (TECs) remains unclear. Here we show that similarly to regular thymocytes, developing B cells enforced to express the Notch ligand Delta-like-1 (DLL1) efficiently induce the non-polarized, three-dimensional (3D) meshwork architecture of cortical TECs in fetal thymic organ culture. Moreover, the DLL1-overexpressing B cells induce well-developed distinct medullae. Such medullae also arose in lobes reconstituted with Rag2-/- thymocytes overexpressing DLL1. Our present findings thus strongly suggest that Notch signaling from thymocytes to TECs induces TEC development at an early phase of thymic organogenesis. The present approach using non-T lineage cells for the in vitro construction of thymic environments may also provide a novel tool for thymus regeneration and T cell production in immunocompromised individuals.
AB - The development and maintenance of thymic microenvironments depends on sustained crosstalk signals derived from developing thymocytes. However, the molecular basis for the initial phase in the lymphoid dependent development of thymic epithelial cells (TECs) remains unclear. Here we show that similarly to regular thymocytes, developing B cells enforced to express the Notch ligand Delta-like-1 (DLL1) efficiently induce the non-polarized, three-dimensional (3D) meshwork architecture of cortical TECs in fetal thymic organ culture. Moreover, the DLL1-overexpressing B cells induce well-developed distinct medullae. Such medullae also arose in lobes reconstituted with Rag2-/- thymocytes overexpressing DLL1. Our present findings thus strongly suggest that Notch signaling from thymocytes to TECs induces TEC development at an early phase of thymic organogenesis. The present approach using non-T lineage cells for the in vitro construction of thymic environments may also provide a novel tool for thymus regeneration and T cell production in immunocompromised individuals.
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U2 - 10.1016/j.molimm.2009.01.015
DO - 10.1016/j.molimm.2009.01.015
M3 - Article
C2 - 19250680
AN - SCOPUS:64149093045
SN - 0161-5890
VL - 46
SP - 1756
EP - 1767
JO - Molecular Immunology
JF - Molecular Immunology
IS - 8-9
ER -