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

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作者
Sonya A. MacParland
Jeff C. Liu
Xue-Zhong Ma
Brendan T. Innes
Agata M. Bartczak
Blair K. Gage
Justin Manuel
Nicholas Khuu
Juan Echeverri
Ivan Linares
Rahul Gupta
Michael L. Cheng
Lewis Y. Liu
Damra Camat
Sai W. Chung
Rebecca K. Seliga
Zigong Shao
Elizabeth Lee
Shinichiro Ogawa
Mina Ogawa
Michael D. Wilson
Jason E. Fish
Markus Selzner
Anand Ghanekar
David Grant
Paul Greig
Gonzalo Sapisochin
Nazia Selzner
Neil Winegarden
Oyedele Adeyi
Gordon Keller
Gary D. Bader
Ian D. McGilvray
机构
[1] Toronto General Hospital Research Institute,Multi
[2] University of Toronto,Organ Transplant Program
[3] University of Toronto,Department of Immunology
[4] University of Toronto,Department of Laboratory Medicine and Pathobiology
[5] University of Toronto,The Donnelly Centre
[6] University Health Network,Department of Molecular Genetics
[7] University Health Network,McEwen Centre for Regenerative Medicine
[8] Hospital for Sick Children,Princess Margaret Genomics Centre
[9] Toronto General Hospital Research Institute,Genetics and Genome Biology
[10] University Health Network,Division of Advanced Diagnostics
[11] Toronto,Laboratory Medicine Program
[12] University Health Network,Princess Margaret Cancer Centre
[13] Toronto,Department of Medical Biophysics
[14] University of Toronto,undefined
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摘要
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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