Scientific reports · 2016
An Essential Role for the Transcription Factor Runx1 in T Cell Maturation.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Hsu Fan-Chi, Shapiro Michael J, Dash Barsha, Chen Chien-Chang, Constans Megan M, Chung Ji Young, Romero Arocha Sinibaldo R, Belmonte Paul J, Chen Meibo W, McWilliams Douglas C, Shapiro Virginia Smith
Аннотация
The transcription factor Runx1 has essential roles throughout hematopoiesis. Here, we demonstrate that Runx1 is critical for T cell maturation. Peripheral naïve CD4(+) T cells from CD4-cre Runx1 cKO mice are phenotypically and functionally immature as shown by decreased production of TNF-α upon TCR stimulation. The loss of peripheral CD4(+) T cells in CD4-cre Runx1 cKO mice is not due to defects in homeostasis or decreased expression of IL-7Rα, as transgenic expression of IL-7Rα does not rescue the loss of CD4(+) T cells. Rather, immature Runx1-deficient CD4(+) T cells are eliminated in the periphery by the activation and fixation of the classical complement pathway. In the thymus, there is a severe block in all aspects of intrathymic T cell maturation, although both positive and negative selection are unaltered. Thus, loss of Runx1 leads to the earliest characterized block in post-positive selection intrathymic maturation of CD4 T cells.
Предметные рубрики MeSH
AnimalsCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedComplement Pathway, ClassicalComplement System ProteinsCore Binding Factor Alpha 2 SubunitFlow CytometryGlycosylationMice, Inbred C57BLMice, KnockoutMice, TransgenicN-Acetylneuraminic AcidReceptors, Interleukin-7Reverse Transcriptase Polymerase Chain ReactionT-Lymphocyte SubsetsThymocytesTumor Necrosis Factor-alpha