| Literature DB >> 31019259 |
Rushika C Wirasinha1, Anna Chan1, Jin Yan Yap2, Daniel Y Hu2, Charis E Teh3,4, Daniel H D Gray3,4, Christopher C Goodnow5,6, Stephen R Daley7.
Abstract
The selection of αβ T cells in the thymus is punctuated by checkpoints at which thymocytes differentiate or undergo apoptosis. Wave 1 deletion is defined as apoptosis within nascent αβ T-cell antigen receptor (TCR)-signalled thymocytes that lack CCR7 expression. The antigen-presenting cell (APC) types that mediate wave 1 deletion are unclear. To measure wave 1 deletion, we compared the frequencies of TCRβ + CD5 + Helios + CCR7- cells in nascent thymocyte cohorts in mice with normal or defective apoptosis. This thymocyte population is small in mice lacking major histocompatibility complex (MHC) expression. The scale of wave 1 deletion was increased by transgenic expression of the self-reactive Yae62 TCRβ chain, was almost halved when haemopoietic APCs lacked MHC expression and, surprisingly, was unchanged when epithelial cells lacked MHC expression. These findings demonstrate efficiency, and some redundancy, in the APC types that mediate wave 1 deletion in the normal mouse thymus.Entities:
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Year: 2019 PMID: 31019259 PMCID: PMC7224288 DOI: 10.1038/s41418-019-0331-8
Source DB: PubMed Journal: Cell Death Differ ISSN: 1350-9047 Impact factor: 15.828