A single-cell survey of the small intestinal epithelium
Name
nihms910777.pdf
Size
5.76 MB
Format
Adobe PDF
Checksum (MD5)
270b85e9730255f2acdc7c8b830dec7a
Author(s) • • • • • • • • •
Haber, Adam L.
Biton, Moshe
Rogel, Noga
Herbst, Rebecca H.
Shekhar, Karthik
Smillie, Christopher
Burgin, Grace
Delorey, Toni M.
Howitt, Michael R.
Katz, Yarden
Date Issued
November 2017
Journal
Nature
Publisher
Nature Publishing Group
Citation
Haber, Adam L. et al. “A Single-Cell Survey of the Small Intestinal Epithelium.” Nature 551, 7680 (November 2017): 333–339 © 2017 Macmillan Publishers Limited, part of Springer Nature
Version
Author's final manuscript
Abstract
Intestinal epithelial cells absorb nutrients, respond to microbes, function as a barrier and help to coordinate immune responses. Here we report profiling of 53,193 individual epithelial cells from the small intestine and organoids of mice, which enabled the identification and characterization of previously unknown subtypes of intestinal epithelial cell and their gene signatures. We found unexpected diversity in hormone-secreting enteroendocrine cells and constructed the taxonomy of newly identified subtypes, and distinguished between two subtypes of tuft cell, one of which expresses the epithelial cytokine Tslp and the pan-immune marker CD45, which was not previously associated with non-haematopoietic cells. We also characterized the ways in which cell-intrinsic states and the proportions of different cell types respond to bacterial and helminth infections: Salmonella infection caused an increase in the abundance of Paneth cells and enterocytes, and broad activation of an antimicrobial program; Heligmosomoides polygyrus caused an increase in the abundance of goblet and tuft cells. Our survey highlights previously unidentified markers and programs, associates sensory molecules with cell types, and uncovers principles of gut homeostasis and response to pathogens.
MIT Department
Massachusetts Institute of Technology. Department of Biology
Koch Institute for Integrative Cancer Research at MIT
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1038/NATURE24489