AI Article Synopsis

  • Mature single positive (SP) thymocytes exit the thymus as recent thymic emigrants (RTEs), which are initially phenotypically and functionally immature, and they undergo further maturation in peripheral lymphoid organs before becoming resident naïve T cells.
  • Researchers identified CD4(+) pre-RTEs, a subset of SP thymocytes poised for egress, showing better survival and faster proliferation compared to peripheral naïve T cells, possibly due to differences in Bcl2/Bim expression and enhanced IL-7 signaling.
  • Upregulation of the Qa2 molecule in CD4(+) pre-RTEs, indicating their maturation, relies on the influence of migratory dendritic cells in the thymic perivascular space,

Article Abstract

After a tightly regulated developmental program in the thymus, "mature" single positive (SP) thymocytes leave the thymus and enter the periphery. These newly arrived recent thymic emigrants (RTEs) are phenotypically and functionally immature, and will complete a dynamic maturation in the peripheral lymphoid organs before being licensed to be resident naïve T cells. To study the early events occurring in the RTE maturation process, we identified the phenotype of CD4(+) pre-RTEs, a population of CD4(+) SP thymocytes that have acquired the thymus egress capability. Compared to peripheral naïve T cells, CD4(+) pre-RTEs displayed superior survival capability in lymphoreplete mice and faster proliferation under lymphopenic condition. The differences in Bcl2/Bim expression and/or heightened IL-7 signaling pathway may account for the pre-RTEs' better responsiveness to homeostatic signals. Qa2, the expression of which indicates the phenotypic maturation of SPs and RTEs, was found to be upregulated in CD4(+) pre-RTEs in thymic perivascular space. Migratory dendritic cells that surround this region contribute to Qa2 expression in pre-RTEs. The dendritic cell-driven Qa2 induction of CD4(+) pre-RTEs is independent of MHC class II and Aire molecules.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569422PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0056378PLOS

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