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author Elmentaite, Rasa
Kumasaka, Natsuhiko
Roberts, Kenny
Fleming, Aaron
Dann, Emma
King, Hamish W.
Kleshchevnikov, Vitalii
Dabrowska, Monika
Pritchard, Sophie
Bolt, Liam
Vieira, Sara F.
Mamanova, Lira
Huang, Ni
Perrone, Francesca
Goh Kai’En, Issac
Lisgo, Steven N.
Katan, Matilda
Leonard, Steven
Oliver, Thomas R. W.
Hook, C. Elizabeth
Nayak, Komal
Campos, Lia S.
Domínguez Conde, Cecilia
Stephenson, Emily
Engelbert, Justin
Botting, Rachel A.
Polanski, Krzysztof
van Dongen, Stijn
Patel, Minal
Morgan, Michael D.
Marioni, John C.
Bayraktar, Omer Ali
Meyer, Kerstin B.
He, Xiaoling
Barker, Roger A.
Uhlig, Holm H.
Mahbubani, Krishnaa T.
Saeb-Parsy, Kourosh
Zilbauer, Matthias
Clatworthy, Menna R.
Haniffa, Muzlifah
James, Kylie R.
Teichmann, Sarah A.
author_facet Elmentaite, Rasa
Kumasaka, Natsuhiko
Roberts, Kenny
Fleming, Aaron
Dann, Emma
King, Hamish W.
Kleshchevnikov, Vitalii
Dabrowska, Monika
Pritchard, Sophie
Bolt, Liam
Vieira, Sara F.
Mamanova, Lira
Huang, Ni
Perrone, Francesca
Goh Kai’En, Issac
Lisgo, Steven N.
Katan, Matilda
Leonard, Steven
Oliver, Thomas R. W.
Hook, C. Elizabeth
Nayak, Komal
Campos, Lia S.
Domínguez Conde, Cecilia
Stephenson, Emily
Engelbert, Justin
Botting, Rachel A.
Polanski, Krzysztof
van Dongen, Stijn
Patel, Minal
Morgan, Michael D.
Marioni, John C.
Bayraktar, Omer Ali
Meyer, Kerstin B.
He, Xiaoling
Barker, Roger A.
Uhlig, Holm H.
Mahbubani, Krishnaa T.
Saeb-Parsy, Kourosh
Zilbauer, Matthias
Clatworthy, Menna R.
Haniffa, Muzlifah
James, Kylie R.
Teichmann, Sarah A.
author_sort Elmentaite, Rasa
collection PubMed
description The cellular landscape of the human intestinal tract is dynamic throughout life, developing in utero and changing in response to functional requirements and environmental exposures. Here, to comprehensively map cell lineages, we use single-cell RNA sequencing and antigen receptor analysis of almost half a million cells from up to 5 anatomical regions in the developing and up to 11 distinct anatomical regions in the healthy paediatric and adult human gut. This reveals the existence of transcriptionally distinct BEST4 epithelial cells throughout the human intestinal tract. Furthermore, we implicate IgG sensing as a function of intestinal tuft cells. We describe neural cell populations in the developing enteric nervous system, and predict cell-type-specific expression of genes associated with Hirschsprung’s disease. Finally, using a systems approach, we identify key cell players that drive the formation of secondary lymphoid tissue in early human development. We show that these programs are adopted in inflammatory bowel disease to recruit and retain immune cells at the site of inflammation. This catalogue of intestinal cells will provide new insights into cellular programs in development, homeostasis and disease.
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spelling pubmed-84261862021-09-27 Cells of the human intestinal tract mapped across space and time Elmentaite, Rasa Kumasaka, Natsuhiko Roberts, Kenny Fleming, Aaron Dann, Emma King, Hamish W. Kleshchevnikov, Vitalii Dabrowska, Monika Pritchard, Sophie Bolt, Liam Vieira, Sara F. Mamanova, Lira Huang, Ni Perrone, Francesca Goh Kai’En, Issac Lisgo, Steven N. Katan, Matilda Leonard, Steven Oliver, Thomas R. W. Hook, C. Elizabeth Nayak, Komal Campos, Lia S. Domínguez Conde, Cecilia Stephenson, Emily Engelbert, Justin Botting, Rachel A. Polanski, Krzysztof van Dongen, Stijn Patel, Minal Morgan, Michael D. Marioni, John C. Bayraktar, Omer Ali Meyer, Kerstin B. He, Xiaoling Barker, Roger A. Uhlig, Holm H. Mahbubani, Krishnaa T. Saeb-Parsy, Kourosh Zilbauer, Matthias Clatworthy, Menna R. Haniffa, Muzlifah James, Kylie R. Teichmann, Sarah A. Nature Article The cellular landscape of the human intestinal tract is dynamic throughout life, developing in utero and changing in response to functional requirements and environmental exposures. Here, to comprehensively map cell lineages, we use single-cell RNA sequencing and antigen receptor analysis of almost half a million cells from up to 5 anatomical regions in the developing and up to 11 distinct anatomical regions in the healthy paediatric and adult human gut. This reveals the existence of transcriptionally distinct BEST4 epithelial cells throughout the human intestinal tract. Furthermore, we implicate IgG sensing as a function of intestinal tuft cells. We describe neural cell populations in the developing enteric nervous system, and predict cell-type-specific expression of genes associated with Hirschsprung’s disease. Finally, using a systems approach, we identify key cell players that drive the formation of secondary lymphoid tissue in early human development. We show that these programs are adopted in inflammatory bowel disease to recruit and retain immune cells at the site of inflammation. This catalogue of intestinal cells will provide new insights into cellular programs in development, homeostasis and disease. Nature Publishing Group UK 2021-09-08 2021 /pmc/articles/PMC8426186/ /pubmed/34497389 http://dx.doi.org/10.1038/s41586-021-03852-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Elmentaite, Rasa
Kumasaka, Natsuhiko
Roberts, Kenny
Fleming, Aaron
Dann, Emma
King, Hamish W.
Kleshchevnikov, Vitalii
Dabrowska, Monika
Pritchard, Sophie
Bolt, Liam
Vieira, Sara F.
Mamanova, Lira
Huang, Ni
Perrone, Francesca
Goh Kai’En, Issac
Lisgo, Steven N.
Katan, Matilda
Leonard, Steven
Oliver, Thomas R. W.
Hook, C. Elizabeth
Nayak, Komal
Campos, Lia S.
Domínguez Conde, Cecilia
Stephenson, Emily
Engelbert, Justin
Botting, Rachel A.
Polanski, Krzysztof
van Dongen, Stijn
Patel, Minal
Morgan, Michael D.
Marioni, John C.
Bayraktar, Omer Ali
Meyer, Kerstin B.
He, Xiaoling
Barker, Roger A.
Uhlig, Holm H.
Mahbubani, Krishnaa T.
Saeb-Parsy, Kourosh
Zilbauer, Matthias
Clatworthy, Menna R.
Haniffa, Muzlifah
James, Kylie R.
Teichmann, Sarah A.
Cells of the human intestinal tract mapped across space and time
title Cells of the human intestinal tract mapped across space and time
title_full Cells of the human intestinal tract mapped across space and time
title_fullStr Cells of the human intestinal tract mapped across space and time
title_full_unstemmed Cells of the human intestinal tract mapped across space and time
title_short Cells of the human intestinal tract mapped across space and time
title_sort cells of the human intestinal tract mapped across space and time
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426186/
https://www.ncbi.nlm.nih.gov/pubmed/34497389
http://dx.doi.org/10.1038/s41586-021-03852-1
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