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A timeline demarcating two waves of clonal deletion and Foxp3 upregulation during thymocyte development

Authors :
Hu, Daniel Y.
Yap, Jin Y.
Wirasinha, R.C.
Howard, Debbie R.
Goodnow, C.C.
Daley, S.R.
Hu, Daniel Y.
Yap, Jin Y.
Wirasinha, R.C.
Howard, Debbie R.
Goodnow, C.C.
Daley, S.R.
Source :
Immunology and Cell Biology
Publication Year :
2016

Abstract

Thymocytes that bind strongly to self‐antigens are prevented from becoming naive T cells by several mechanisms. They undergo clonal deletion at two stages of development; wave 1 in immature thymocytes lacking the medulla‐homing chemokine receptor, CCR7, or wave 2 in more mature CCR7+ thymocytes. Alternatively, self‐reactive thymocytes upregulate Foxp3 to become T‐regulatory cells. Here, we describe the differential timing of the two waves of deletion and Foxp3 upregulation relative to the immature proliferating stage. Proliferating thymocytes were pulse‐labeled in normal C57BL/6 mice with 5‐ethynyl‐2'‐deoxyuridine (EdU). Thymocytes progressed into wave 1 (CCR7−) and wave 2 (CCR7+) of clonal deletion ~2 and 5 days after proliferation, respectively. Foxp3 upregulation occurred between 4 and 8 days after proliferation, predominantly in thymocytes with a Helios+ CCR7+ phenotype. These findings establish a timeline that suggests that wave 1 of clonal deletion occurs in the thymic cortex, whereas wave 2 and Foxp3 upregulation both occur in the thymic medulla.

Details

Database :
OAIster
Journal :
Immunology and Cell Biology
Publication Type :
Electronic Resource
Accession number :
edsoai.on1255559111
Document Type :
Electronic Resource