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      A single-cell survey of the small intestinal epithelium

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          Abstract

          Intestinal epithelial cells (IECs) absorb nutrients, respond to microbes, provide barrier function and help coordinate immune responses. We profiled 53,193 individual epithelial cells from mouse small intestine and organoids, and characterized novel subtypes and their gene signatures. We showed unexpected diversity of hormone-secreting enteroendocrine cells and constructed their novel taxonomy. We distinguished between two tuft cell subtypes, one of which expresses the epithelial cytokine TSLP and CD45 ( Ptprc), the pan-immune marker not previously associated with non-hematopoietic cells. We also characterized how cell-intrinsic states and cell proportions respond to bacterial and helminth infections. Salmonella infection caused an increase in Paneth cells and enterocytes abundance, and broad activation of an antimicrobial program. In contrast, Heligmosomoides polygyrus caused an expansion of goblet and tuft cell populations. Our survey highlights new markers and programs, associates sensory molecules to cell types, and uncovers principles of gut homeostasis and response to pathogens.

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          Most cited references36

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            NIH Image to ImageJ: 25 years of image analysis.

            For the past 25 years NIH Image and ImageJ software have been pioneers as open tools for the analysis of scientific images. We discuss the origins, challenges and solutions of these two programs, and how their history can serve to advise and inform other software projects.
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              Tuft-cell-derived IL-25 regulates an intestinal ILC2-epithelial response circuit.

              Parasitic helminths and allergens induce a type 2 immune response leading to profound changes in tissue physiology, including hyperplasia of mucus-secreting goblet cells and smooth muscle hypercontractility. This response, known as 'weep and sweep', requires interleukin (IL)-13 production by tissue-resident group 2 innate lymphoid cells (ILC2s) and recruited type 2 helper T cells (TH2 cells). Experiments in mice and humans have demonstrated requirements for the epithelial cytokines IL-33, thymic stromal lymphopoietin (TSLP) and IL-25 in the activation of ILC2s, but the sources and regulation of these signals remain poorly defined. In the small intestine, the epithelium consists of at least five distinct cellular lineages, including the tuft cell, whose function is unclear. Here we show that tuft cells constitutively express IL-25 to sustain ILC2 homeostasis in the resting lamina propria in mice. After helminth infection, tuft-cell-derived IL-25 further activates ILC2s to secrete IL-13, which acts on epithelial crypt progenitors to promote differentiation of tuft and goblet cells, leading to increased frequencies of both. Tuft cells, ILC2s and epithelial progenitors therefore comprise a response circuit that mediates epithelial remodelling associated with type 2 immunity in the small intestine, and perhaps at other mucosal barriers populated by these cells.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                12 June 2018
                08 November 2017
                16 November 2017
                28 June 2018
                : 551
                : 7680
                : 333-339
                Affiliations
                [1 ]Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA
                [2 ]Center for Computational and Integrative Biology, Massachusetts General Hospital, Boston, MA, 02114, USA
                [3 ]Department of Systems Biology, Harvard Medical School, Boston, MA 02114, USA
                [4 ]Department of Biology and Biotechnology, Worcester Polytechnic Institute, Worcester, MA 01609, USA
                [5 ]Departments of Immunology and Infectious Diseases and Genetics and Complex Diseases, Harvard T. H. Chan School of Public Health, Boston, MA 02115, USA
                [6 ]The David H. Koch Institute for Integrative Cancer Research at MIT, Department of Biology, MIT, Cambridge, Massachusetts 02139, USA
                [7 ]Division of Hematology/Oncology, Boston Children’s Hospital and Department of Pediatric Oncology, Dana-Farber Cancer Institute, Howard Hughes Medical Institute, Harvard Stem Cell Institute, Harvard Medical School, Boston, Massachusetts 02115, USA
                [8 ]Mucosal Immunology and Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, 02129, USA
                [9 ]New York Genome Center, New York University Center for Genomics and Systems Biology, New York, NY, USA
                [10 ]New York University Center for Genomics and Systems Biology, New York, NY, USA
                [11 ]Departments of Pathology, Gastroenterology, and Surgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA
                [12 ]Gastrointestinal Unit and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital, Boston, MA, 02114, USA
                [13 ]Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02140, USA
                Author notes
                [*]

                These authors contributed equally to this work.

                [§]

                Co-senior authors.

                Correspondence and requests for materials should be addressed to M.B. ( mbiton@ 123456broadinstitute.org ), R.J.X. ( xavier@ 123456molbio.mgh.harvard.edu ), and A.R. ( aregev@ 123456broadinstitute.org ).

                Article
                NIHMS910777
                10.1038/nature24489
                6022292
                29144463
                4e791503-0675-4d8d-be38-56fd9cddb23f

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