Evidence map›Paper›PMID 27828940›Full record

ArticleNature2016

Different tissue phagocytes sample apoptotic cells to direct distinct homeostasis programs.

Ryan J Cummings, Gaetan Barbet, Gerold Bongers, Boris M Hartmann, Kyle Gettler, Luciana Muniz, Glaucia C Furtado, Judy Cho, Sergio A Lira, J Magarian Blander

Open access · greenAbstract read
In one paragraph

Article in Nature, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 147 papers.

0numbers the graph read from it
0cells of the map it votes in
147citing papers in PubMed
9.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

147 citing papers in PubMed, 217 citations in OpenAlex.

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  15. Article
  16. Submicron-Sampling of Living Cells by Macrophages.bioRxiv : the preprint server for biology · 2025
    Article
  17. Review
  18. Review
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87 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Ryan J CummingsImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Gaetan BarbetImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Gerold BongersImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Boris M HartmannDepartment of Neurology, Center for Translational Systems Biology, Icahn School of Medicine at Mount Sinai, New York 10029, USA.
Kyle GettlerDepartment of Genetics, Yale School of Medicine, New Haven, Connecticut 06520, USA.
Luciana MunizImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Glaucia C FurtadoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Judy ChoImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Sergio A LiraImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
J Magarian BlanderImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Icahn School of Medicine at Mount Sinai · USTisch Hospital · USYale University · US

Funding

Inflammatory Bowel Disease Genetics Consortium Data Coordinating CenterU01DK062429 · NIDDK · YALE UNIVERSITY · PI CHO, JUDY H. · 2002 to 2016
$16.8M
THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSEP01DK072201 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HARPAZ, NOAM · 2006 to 2015
$14.6M
Yale University Inflammatory Bowel Disease Genetics Research CenterU01DK062422 · NIDDK · YALE UNIVERSITY · PI Ling-shiang Chuang · 2002 to 2026
$10.8M
Project I: Immunity to Influenza in Primary Lung Epithelial CellsU19AI117873 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HAYOT, FERNAND · 2015 to 2019
$8.6M
GENETICS AND GENOMICS OF HUMAN DISEASET32HD007149 · NICHD · YALE UNIVERSITY · PI James P Noonan · 1985 to 2026
$8.2M
Mechanisms associated with flares and remission in colitisR01DK110352 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2017 to 2025
$5.1M
Molecular pathogenesis of intestinal serrated polypsR01CA161373 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2011 to 2020
$3.7M
Defining the genetic architecture of IBD in Ashkenazi Jewish populationsR01DK092235 · NIDDK · YALE UNIVERSITY · PI CHO, JUDY H. · 2012 to 2016
$2.5M
TRAINING PROGRAM IN INVESTIGATIVE GASTROENTEROLOGYT32DK007792 · NIDDK · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI CHO, JUDY H. · 2001 to 2016
$2.3M
Non-Canonical Cross-presentation in Dendritic Cells Upon TAP BlockadeR01AI123284 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLANDER, JULIE MAGARIAN · 2016 to 2020
$2.1M
Control of protective immunity by innate pathways sensing bacterial viabilityR01AI095245 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BLANDER, JULIE MAGARIAN · 2012 to 2015
$1.7M
Role of apoptosis in the intestinal epithelium during homeostasis and diseaseR01DK111862 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLANDER, JULIE MAGARIAN · 2017 to 2020
$1.5M
NCI NIH HHS R01 CA161373NIAID NIH HHS HHSN272201000054CNIAID NIH HHS R01 AI095245NIAID NIH HHS R01 AI123284NIAID NIH HHS U19 AI117873NICHD NIH HHS T32 HD007149NIDDK NIH HHS P01 DK072201NIDDK NIH HHS R01 DK092235NIDDK NIH HHS R01 DK110352NIDDK NIH HHS R01 DK111862NIDDK NIH HHS T32 DK007792NIDDK NIH HHS U01 DK062422NIDDK NIH HHS U01 DK062429NIH HHS 2T32A1007605-11NIH HHS 5P01DK072201-09NIH HHS 5R01CA161373-04NIH HHS 5T32DK007792-12NIH HHS AI095245NIH HHS AI123284NIH HHS DK072201
6 · The paper itself

Abstract

Recognition and removal of apoptotic cells by professional phagocytes, including dendritic cells and macrophages, preserves immune self-tolerance and prevents chronic inflammation and autoimmune pathologies. The diverse array of phagocytes that reside within different tissues, combined with the necessarily prompt nature of apoptotic cell clearance, makes it difficult to study this process in situ. The full spectrum of functions executed by tissue-resident phagocytes in response to homeostatic apoptosis, therefore, remains unclear. Here we show that mouse apoptotic intestinal epithelial cells (IECs), which undergo continuous renewal to maintain optimal barrier and absorptive functions, are not merely extruded to maintain homeostatic cell numbers, but are also sampled by a single subset of dendritic cells and two macrophage subsets within a well-characterized network of phagocytes in the small intestinal lamina propria. Characterization of the transcriptome within each subset before and after in situ sampling of apoptotic IECs revealed gene expression signatures unique to each phagocyte, including macrophage-specific lipid metabolism and amino acid catabolism, and a dendritic-cell-specific program of regulatory CD4

Indexed as

ApoptosisHomeostasisAmino AcidsAnimalsAntigens, CDCD4-Positive T-LymphocytesCell DifferentiationCell MovementDendritic CellsEpithelial CellsFemaleInflammationInflammatory Bowel DiseasesIntegrin alpha ChainsIntestinal MucosaLipid Metabolismalpha E integrinsAmino AcidsAntigens, CDIntegrin alpha Chains

Identifiers

PMID27828940
PMCPMC5807003
OpenAlexW2556519132

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.