先天性淋巴细胞
神经肽1
生物
免疫学
血管生成
淋巴系统
细胞生物学
免疫系统
血管内皮生长因子
癌症研究
先天免疫系统
血管内皮生长因子受体
作者
Medya Shikhagaie,Åsa K. Björklund,Jenny Mjösberg,Jonas S. Erjefält,Anne Cornelissen,Xavier Bofill-De Ros,Suzanne M. Bal,Jasper J. Koning,Reina E. Mebius,Michiko Mori,Mélanie Bruchard,Bianca Blom,Hergen Spits
出处
期刊:Cell Reports
[Elsevier]
日期:2017-02-14
卷期号:18 (7): 1761-1773
被引量:76
标识
DOI:10.1016/j.celrep.2017.01.063
摘要
Here, we characterize a subset of ILC3s that express Neuropilin1 (NRP1) and are present in lymphoid tissues, but not in the peripheral blood or skin. NRP1+ group 3 innate lymphoid cells (ILC3s) display in vitro lymphoid tissue inducer (LTi) activity. In agreement with this, NRP1+ ILC3s are mainly located in proximity to high endothelial venules (HEVs) and express cell surface molecules involved in lymphocyte migration in secondary lymphoid tissues via HEVs. NRP1 was also expressed on mouse fetal LTi cells, indicating that NRP1 is a conserved marker for LTi cells. Human NRP1+ ILC3s are primed cells because they express CD45RO and produce higher amounts of cytokines than NRP1- cells, which express CD45RA. The NRP1 ligand vascular endothelial growth factor A (VEGF-A) served as a chemotactic factor for NRP1+ ILC3s. NRP1+ ILC3s are present in lung tissues from smokers and patients with chronic obstructive pulmonary disease, suggesting a role in angiogenesis and/or the initiation of ectopic pulmonary lymphoid aggregates.
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