流感感染期间肺淋巴内皮细胞和淋巴反应的单细胞分析

Jian Ge, Hongxia Shao, Hongxu Ding, Yuefeng Huang, Xuebing Wu, Jie Sun, Jianwen Que
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引用次数: 0

摘要

组织淋巴管网在应对病原体入侵的免疫监视和组织稳态中发挥着关键作用,但人们对感染期间淋巴系统本身是如何重塑的却知之甚少。在这里,我们观察到流感感染会诱导肺部淋巴管数量显著增加,并伴随着淋巴内皮细胞(LECs)的广泛增殖。单细胞 RNA 测序显示了淋巴管内皮细胞的异质性,确定了一个新的 PD-L1+ 亚群,该亚群在病毒感染期间存在,但在稳态时并不存在。在 LECs 中特异性地删除 Pd-l1 可提高病毒感染期间淋巴管数量的扩张。这些发现共同阐明了肺淋巴管网在病毒感染时的急剧扩张,并揭示了一个可能调节淋巴管重塑的PD-L1+ LEC亚群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Single Cell Analysis of Lung Lymphatic Endothelial Cells and Lymphatic Responses during Influenza Infection.

Tissue lymphatic vessels network plays critical roles in immune surveillance and tissue homeostasis in response to pathogen invasion, but how lymphatic system per se is remolded during infection is less understood. Here, we observed that influenza infection induces a significant increase of lymphatic vessel numbers in the lung, accompanied with extensive proliferation of lymphatic endothelial cells (LECs). Single-cell RNA sequencing illustrated the heterogeneity of LECs, identifying a novel PD-L1+ subpopulation that is present during viral infection but not at steady state. Specific deletion of Pd-l1 in LECs elevated the expansion of lymphatic vessel numbers during viral infection. Together these findings elucidate a dramatic expansion of lung lymphatic network in response to viral infection, and reveal a PD-L1+ LEC subpopulation that potentially modulates lymphatic vessel remolding.

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