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Characterization of the thymic IL-7 niche in vivo.

Abstract : The thymus represents the "cradle" for T cell development, with thymic stroma providing multiple soluble and membrane cues to developing thymocytes. Although IL-7 is recognized as an essential factor for thymopoiesis, the "environmental niche" of thymic IL-7 activity remains poorly characterized in vivo. Using bacterial artificial chromosome transgenic mice in which YFP is under control of IL-7 promoter, we identify a subset of thymic epithelial cells (TECs) that co-express YFP and high levels of Il7 transcripts (IL-7(hi) cells). IL-7(hi) TECs arise during early fetal development, persist throughout life, and co-express homeostatic chemokines (Ccl19, Ccl25, Cxcl12) and cytokines (Il15) that are critical for normal thymopoiesis. In the adult thymus, IL-7(hi) cells localize to the cortico-medullary junction and display traits of both cortical and medullary TECs. Interestingly, the frequency of IL-7(hi) cells decreases with age, suggesting a mechanism for the age-related thymic involution that is associated with declining IL-7 levels. Our temporal-spatial analysis of IL-7-producing cells in the thymus in vivo suggests that thymic IL-7 levels are dynamically regulated under distinct physiological conditions. This IL-7 reporter mouse provides a valuable tool to further dissect the mechanisms that govern thymic IL-7 expression in vivo.
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https://hal-pasteur.archives-ouvertes.fr/pasteur-00428982
Contributor : Marie-Christine Vougny <>
Submitted on : Friday, October 30, 2009 - 11:22:52 AM
Last modification on : Thursday, June 18, 2020 - 5:38:02 PM

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Nuno L. Alves, Odile Richard-Le Goff, Nicholas D. Huntington, Ana Patricia Sousa, Vera S. G. Ribeiro, et al.. Characterization of the thymic IL-7 niche in vivo.. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2009, 106 (5), pp.1512-7. ⟨10.1073/pnas.0809559106⟩. ⟨pasteur-00428982⟩

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