高内皮静脉
淋巴
网状细胞
化学
细胞迁移
淋巴结
CD11c公司
活体显微镜检查
细胞生物学
分子生物学
病理
生物
细胞
免疫学
医学
表型
微循环
内科学
基因
生物化学
脾脏
作者
Kibaek Choe,Jieun Moon,Soo Yun Lee,Eunjoo Song,Ju Hee Back,Joo‐Hye Song,Young‐Min Hyun,Kenji Uchimura,Pilhan Kim
出处
期刊:Life science alliance
[Life Science Alliance]
日期:2021-06-29
卷期号:4 (8): e202101086-e202101086
被引量:10
标识
DOI:10.26508/lsa.202101086
摘要
High endothelial venules (HEVs) effectively recruit circulating lymphocytes from the blood to lymph nodes. HEVs have endothelial cells (ECs) and perivascular sheaths consisting of fibroblastic reticular cells (FRCs). Yet, post-luminal lymphocyte migration steps are not well elucidated. Herein, we performed intravital imaging to investigate post-luminal T- and B-cell migration in popliteal lymph node, consisting of trans-EC migration, crawling in the perivascular channel (a narrow space between ECs and FRCs) and trans-FRC migration. The post-luminal migration of T cells occurred in a PNAd-dependent manner. Remarkably, we found hot spots for the trans-EC and trans-FRC migration of T- and B cells. Interestingly, T- and B cells preferentially shared trans-FRC migration hot spots but not trans-EC migration hot spots. Furthermore, the trans-FRC T-cell migration was confined to fewer sites than trans-EC T-cell migration, and trans-FRC migration of T- and B cells preferentially occurred at FRCs covered by CD11c+ dendritic cells in HEVs. These results suggest that HEV ECs and FRCs with perivascular DCs delicately regulate T- and B-cell entry into peripheral lymph nodes.
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