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IL-7 production in murine lymphatic endothelial cells and induction in the setting of peripheral lymphopenia

机译:小鼠淋巴内皮细胞中IL-7的产生及周围淋巴细胞减少的诱导

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摘要

IL-7 is a required factor for T-cell homeostasis. Because of low expression levels and poor reagent availability, the cellular sources of IL-7 have proven challenging to characterize. In this study, we describe a reporter mouse in which enhanced GFP is expressed from the endogenous Il7 locus. We show that IL-7 is produced by lymphatic endothelial cells (LECs) distributed throughout the systemic lymphatic vasculature as well as by fibroblastic reticular cells, and that phosphorylation of STAT5 in lymphocytes is higher in lymphatics than in blood. Furthermore, in nodes depleted of lymphocytes, Il7 transcription is increased in stromal but not in myeloid subsets. These data support recent findings that lymphocyte homeostasis is influenced by access to secondary lymphoid organs and point to LECs as an important in vivo source of IL-7, bathing trafficking immune cells under both resting and lymphopenic conditions.
机译:IL-7是T细胞稳态的必需因子。由于低表达水平和较差的试剂利用率,IL-7的细胞来源已证明难以表征。在这项研究中,我们描述了一种记者小鼠,其中从内源性Il7基因座表达了增强的GFP。我们表明,IL-7是由分布在全身淋巴管系统中的淋巴管内皮细胞(LEC)以及由成纤维细胞网状细胞产生的,并且淋巴管中的STAT5磷酸化高于血液。此外,在淋巴结耗尽的淋巴结中,间质中Il7转录增加,而髓系亚群中则没有。这些数据支持了最近的发现,即淋巴细胞的稳态受到次生淋巴器官的进入的影响,并指向LECs作为IL-7的重要体内来源,在静息和淋巴细胞减少的条件下浸没运输的免疫细胞。

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