| Literature DB >> 31402260 |
Akira Takeda1, Maija Hollmén1, Denis Dermadi2, Junliang Pan3, Kevin Francis Brulois2, Riina Kaukonen4, Tapio Lönnberg4, Pia Boström5, Ilkka Koskivuo6, Heikki Irjala7, Masayuki Miyasaka8, Marko Salmi1, Eugene C Butcher3, Sirpa Jalkanen9.
Abstract
Lymphatic vessels form a critical component in the regulation of human health and disease. While their functional significance is increasingly being recognized, the comprehensive heterogeneity of lymphatics remains uncharacterized. Here, we report the profiling of 33,000 lymphatic endothelial cells (LECs) in human lymph nodes (LNs) by single-cell RNA sequencing. Unbiased clustering revealed six major types of human LECs. LECs lining the subcapsular sinus (SCS) of LNs abundantly expressed neutrophil chemoattractants, whereas LECs lining the medullary sinus (MS) expressed a C-type lectin CD209. Binding of a carbohydrate Lewis X (CD15) to CD209 mediated neutrophil binding to the MS. The neutrophil-selective homing by MS LECs may retain neutrophils in the LN medulla and allow lymph-borne pathogens to clear, preventing their spread through LNs in humans. Our study provides a comprehensive characterization of LEC heterogeneity and unveils a previously undefined role for medullary LECs in human immunity.Entities:
Keywords: cell adhesion; heterogeneity; human immunity; leukocyte trafficking; lymph nodes; lymphatic endothelial cells; lymphatic vessels; lymphatics; neutrophils; single-cell RNA-seq
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Year: 2019 PMID: 31402260 DOI: 10.1016/j.immuni.2019.06.027
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745