Ge Jian, Shao Hongxia, Ding Hongxu, Huang Yuefeng, Wu Xuebing, Sun Jie, Que Jianwen
Columbia Center for Human Development & Division of Digestive and Liver Diseases, Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.
Haihe Hospital, Tianjin University, Tianjin 300350, China.
J Respir Biol Transl Med. 2024 Mar;1(1). doi: 10.35534/jrbtm.2024.10003. Epub 2024 Feb 19.
Tissue lymphatic vessels network plays critical roles in immune surveillance and tissue homeostasis in response to pathogen invasion, but how lymphatic system 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 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.
组织淋巴管网络在应对病原体入侵时的免疫监视和组织稳态中发挥着关键作用,但对于感染期间淋巴系统如何重塑却知之甚少。在此,我们观察到流感感染会导致肺部淋巴管数量显著增加,并伴有淋巴管内皮细胞(LEC)的广泛增殖。单细胞RNA测序揭示了LEC的异质性,鉴定出一种新型的PD-L1亚群,该亚群在病毒感染期间存在,但在稳态时不存在。在LEC中特异性缺失[此处原文缺失具体基因或蛋白名称]会在病毒感染期间提高淋巴管数量的扩张。这些发现共同阐明了肺部淋巴网络在病毒感染时的显著扩张,并揭示了一个可能调节淋巴管重塑的PD-L1 LEC亚群。