Notch1 deficiency alters the migratory behavior of developing T cells and calcium signaling in the thymus of medaka

被引:1
作者
Aghaallaei, Narges [1 ,2 ]
Inoue, Daigo [2 ]
de Carvalho, Eva Hasel [3 ]
Dick, Advaita M. [1 ]
Wittbrodt, Joachim [2 ]
Leptin, Maria [3 ,4 ]
Bajoghli, Baubak [1 ,3 ]
机构
[1] Univ Hosp Tubingen, Dept Hematol Oncol Immunol & Rheumatol, Tubingen, Germany
[2] Heidelberg Univ, Ctr Organismal Studies COS, Heidelberg, Germany
[3] European Mol Biol Lab EMBL, Heidelberg, Germany
[4] EMBO, Heidelberg, Germany
关键词
Thymus . Cell migration . Notch1 . Medaka . Chemokine receptors; POSITIVELY SELECTED THYMOCYTES; DELTA-LIKE; 4; ALPHA-BETA; EXPRESSION; SELECTION; TCR; SPECIFICATION; INACTIVATION; THYMOPOIESIS; MATURATION;
D O I
10.1002/eji.202149512
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The differentiation of T cells from lymphoid progenitors in the thymus follows sequential developmental stages that constantly require interaction with thymic epithelial cells. Several distinct aspects of early T cell development depend on the activation of Notch receptors on thymocytes, while the selection of thymocytes at later stages are believed to be Notch independent. Using reverse genetic approaches and whole-thymus live imaging in an in vivo teleost model, the medaka, we report that Notch1 signals is required for proliferation and specification of developing T cells as well as involved in their selection in the thymus. We reveal that Notch1 controls the migratory behavior of thymocytes through controlling the chemokine receptor Ccr9b and thereby influence the T cell receptor (TCR) activation. Hence, we propose that, in lower vertebrates, the function of Notch signaling extends to all stages of T cell development, except when thymocytes undergo TCR beta rearrangement.
引用
收藏
页码:261 / 269
页数:9
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