Single cell RNA sequencing of human liver reveals distinct intrahepatic macrophage populations

Sonya A. MacParland(University of Toronto), Jeff C. Liu(University of Toronto), Xue‐Zhong Ma(Toronto General Hospital), Brendan T. Innes(University of Toronto), Agata Bartczak(Toronto General Hospital), Blair K. Gage(University Health Network), Justin Manuel(Toronto General Hospital), Nicholas Khuu(University Health Network), Juan Echeverri(Toronto General Hospital), Ivan Linares(Toronto General Hospital), Rahul Gupta(Toronto General Hospital), Michael Cheng(University of Toronto), Lewis Liu(University of Toronto), Damra Camat(Toronto General Hospital), Sai Chung(University of Toronto), Rebecca K. Seliga(Toronto General Hospital), Zigong Shao(Toronto General Hospital), Elizabeth Lee(Toronto General Hospital), Shinichiro Ogawa(University Health Network), Mina Ogawa(University Health Network), Michael D. Wilson(University of Toronto), Jason E. Fish(University of Toronto), Markus Selzner(Toronto General Hospital), Anand Ghanekar(Toronto General Hospital), David Grant(Toronto General Hospital), Paul D. Greig(Toronto General Hospital), Gonzalo Sapisochín(Toronto General Hospital), Nazia Selzner(Toronto General Hospital), Neil Winegarden(University Health Network), Oyedele Adeyi(University Health Network), Gordon Keller(University Health Network), Gary D. Bader(University of Toronto), Ian D. McGilvray(Toronto General Hospital)
Nature Communications
October 16, 2018
Cited by 1,609Open Access
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Abstract

The liver is the largest solid organ in the body and is critical for metabolic and immune functions. However, little is known about the cells that make up the human liver and its immune microenvironment. Here we report a map of the cellular landscape of the human liver using single-cell RNA sequencing. We provide the transcriptional profiles of 8444 parenchymal and non-parenchymal cells obtained from the fractionation of fresh hepatic tissue from five human livers. Using gene expression patterns, flow cytometry, and immunohistochemical examinations, we identify 20 discrete cell populations of hepatocytes, endothelial cells, cholangiocytes, hepatic stellate cells, B cells, conventional and non-conventional T cells, NK-like cells, and distinct intrahepatic monocyte/macrophage populations. Together, our study presents a comprehensive view of the human liver at single-cell resolution that outlines the characteristics of resident cells in the liver, and in particular provides a map of the human hepatic immune microenvironment.


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