Cells of the human intestinal tract mapped across space and time

Author:

Elmentaite RasaORCID,Kumasaka NatsuhikoORCID,Roberts KennyORCID,Fleming Aaron,Dann EmmaORCID,King Hamish W.ORCID,Kleshchevnikov Vitalii,Dabrowska Monika,Pritchard Sophie,Bolt LiamORCID,Vieira Sara F.ORCID,Mamanova LiraORCID,Huang Ni,Perrone Francesca,Goh Kai’En Issac,Lisgo Steven N.,Katan MatildaORCID,Leonard Steven,Oliver Thomas R. W.ORCID,Hook C. Elizabeth,Nayak Komal,Campos Lia S.,Domínguez Conde CeciliaORCID,Stephenson Emily,Engelbert Justin,Botting Rachel A.ORCID,Polanski KrzysztofORCID,van Dongen Stijn,Patel Minal,Morgan Michael D.ORCID,Marioni John C.ORCID,Bayraktar Omer AliORCID,Meyer Kerstin B.ORCID,He Xiaoling,Barker Roger A.,Uhlig Holm H.ORCID,Mahbubani Krishnaa T.ORCID,Saeb-Parsy KouroshORCID,Zilbauer MatthiasORCID,Clatworthy Menna R.,Haniffa MuzlifahORCID,James Kylie R.ORCID,Teichmann Sarah A.ORCID

Abstract

AbstractThe 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.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3