IL-7 is a major regulator of lymphocyte homeostasis; however, little is known about the mechanisms that regulate IL-7 production. To study Il7 gene regulation in vivo, we generated a novel IL-7-reporter mouse, which allows the non-invasive quantification of Il7 gene activity in live mice and, additionally, the simultaneous activation/inactivation of target genes in IL-7-producing cells. With these IL-7-reporter mice, we identify thymus, skin and intestine as major sources of IL-7 in vivo. Importantly, we show that IFN-γ and the commensal microflora promote steady-state IL-7 production in the intestine. Furthermore, we demonstrate that the blockade of IFN-γ signaling in intestinal epithelial cells strongly reduces their IFN-γ-driven IL-7 production. In summary, our data suggest a feedback loop in which commensal bacteria drive IFN-γ production by lymphocytes, which in turn promotes epithelial cell IL-7 production and the survival of IL-7-dependent lymphocytes. © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
CITATION STYLE
Shalapour, S., Deiser, K., Sercan, Ö., Tuckermann, J., Minnich, K., Willimsky, G., … Schüler, T. (2010). Commensal microflora and interferon-γ promote steady-state interleukin-7 production in vivo. European Journal of Immunology, 40(9), 2391–2400. https://doi.org/10.1002/eji.201040441
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