TY - JOUR
T1 - A single-cell survey of the small intestinal epithelium
AU - Haber, Adam L.
AU - Biton, Moshe
AU - Rogel, Noga
AU - Herbst, Rebecca H.
AU - Shekhar, Karthik
AU - Smillie, Christopher
AU - Burgin, Grace
AU - Delorey, Toni M.
AU - Howitt, Michael R.
AU - Katz, Yarden
AU - Tirosh, Itay
AU - Beyaz, Semir
AU - Dionne, Danielle
AU - Zhang, Mei
AU - Raychowdhury, Raktima
AU - Garrett, Wendy S.
AU - Rozenblatt-Rosen, Orit
AU - Shi, Hai Ning
AU - Yilmaz, Omer
AU - Xavier, Ramnik J.
AU - Regev, Aviv
N1 - We thank L. Gaffney for help with figure preparation, the Broad Flow Cytometry Facility (P. Rogers, S. Saldi and C. Otis), C. Hafemeister and R. Satija for use of the ‘How Many Cells’ tool, S. Riesenfeld and A. Dixit for statistical advice, and T. Tickle for help with the Single Cell Portal. This study was supported by the Klarman Cell Observatory at the Broad Institute, NIH RC2DK114784 (A.R. and R.J.X.), HHMI (A.R.), Food Allergy Science Initiative (FASI) at the Broad Institute (A.R. and R.J.X.), and a Broadnext10 award (A.R. and R.J.X.). M.B. is supported by a postdoctoral fellowship from the Human Frontiers Science Program (HFSP). R.J.X. is supported by NIH DK43351, DK097485 and the Helmsley Charitable Trust. Adam L. Haber, Moshe Biton & Noga Rogel These authors contributed equally to this work. Moshe Biton, Ramnik J. Xavier & Aviv Regev These authors jointly supervised this work.
PY - 2017/11/16
Y1 - 2017/11/16
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85034439213&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/nature24489
DO - https://doi.org/10.1038/nature24489
M3 - مقالة
SN - 0028-0836
VL - 551
SP - 333
EP - 339
JO - Nature
JF - Nature
IS - 7680
ER -