Cells of the human intestinal tract mapped across space and time

Author:

Elmentaite RORCID,Kumasaka N,King HWORCID,Roberts KORCID,Dabrowska M,Pritchard S,Bolt L,Vieira SF,Mamanova LORCID,Huang N,Goh Kai’En IORCID,Stephenson EORCID,Engelbert J,Botting RAORCID,Fleming A,Dann EORCID,Lisgo SNORCID,Katan MORCID,Leonard S,Oliver TRWORCID,Hook CE,Nayak K,Perrone F,Campos LS,Dominguez-Conde CORCID,Polanski KORCID,Van Dongen S,Patel M,Morgan MD,Marioni JCORCID,Bayraktar OAORCID,Meyer KBORCID,Zilbauer MORCID,Uhlig HORCID,Clatworthy MRORCID,Mahbubani KTORCID,Saeb Parsy KORCID,Haniffa MORCID,James KRORCID,Teichmann SAORCID

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. To comprehensively map cell lineages in the healthy developing, pediatric and adult human gut from ten distinct anatomical regions, as well as draining lymph nodes, we used singlecell RNA-seq and VDJ analysis of roughly one third of a million cells. This reveals the presence of BEST4+ absorptive cells throughout the human intestinal tract, demonstrating the existence of this cell type beyond the colon for the first time. Furthermore, we implicate IgG sensing as a novel function of intestinal tuft cells, and link these cells to the pathogenesis of inflammatory bowel disease. We define novel glial and neuronal cell populations in the developing enteric nervous system, and predict cell-type specific expression of Hirschsprung’s disease-associated genes. Finally, using a systems approach, we identify key cell players across multiple cell lineages driving secondary lymphoid tissue formation 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. These data provide an unprecedented catalogue of intestinal cells, and new insights into cellular programs in development, homeostasis and disease.

Publisher

Cold Spring Harbor Laboratory

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