<i>In vivo</i> tracking of T cell development, ablation, and engraftment in transgenic zebrafish

David M. Langenau, Adolfo A. Ferrando, David Traver, Jeffery L. Kutok, John‐Paul D. Hezel, John P. Kanki, Leonard I. Zon, A. Thomas Look, Nikolaus S. Trede

Proceedings of the National Academy of Sciences · 2004 · 445 citations · 34 references

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Abstract

Transgenic zebrafish that express GFP under control of the T cell-specific tyrosine kinase (lck) promoter were used to analyze critical aspects of the immune system, including patterns of T cell development and T cell homing after transplant. GFP-labeled T cells could be ablated in larvae by either irradiation or dexamethasone added to the water, illustrating that T cells have evolutionarily conserved responses to chemical and radiation ablation. In transplant experiments, thymocytes from lck-GFP fish repopulated the thymus of irradiated wild-type fish only transiently, suggesting that the thymus contains only short-term thymic repopulating cells. By contrast, whole kidney marrow permanently reconstituted the T lymphoid compartment of irradiated wild-type fish, suggesting that long-term thymic repopulating cells reside in the kidney.

References

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