Evidence map›Paper›PMID 29925006›Full record

ArticleCell reports2018

Notch Signaling Facilitates In Vitro Generation of Cross-Presenting Classical Dendritic Cells.

Margaret E Kirkling, Urszula Cytlak, Colleen M Lau, Kanako L Lewis, Anastasia Resteu, Alireza Khodadadi-Jamayran, Christian W Siebel, Hélène Salmon, Miriam Merad, Aristotelis Tsirigos and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

123 citing papers in PubMed, 195 citations in OpenAlex.

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63 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Margaret E KirklingDepartment of Pathology, New York University School of Medicine, New York, NY 10016, USA; Graduate Program in Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Urszula CytlakInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Colleen M LauDepartment of Pathology, New York University School of Medicine, New York, NY 10016, USA.
Kanako L LewisDepartment of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA.
Anastasia ResteuInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Alireza Khodadadi-JamayranDepartment of Pathology, New York University School of Medicine, New York, NY 10016, USA; Applied Bioinformatics Laboratories, NYU School of Medicine, NY 10016, USA.
Christian W SiebelGenentech, Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
Hélène SalmonDepartment of Oncological Science, Icahn School of Medicine at Mount Sinai, New York, NY 10028, USA.
Miriam MeradDepartment of Oncological Science, Icahn School of Medicine at Mount Sinai, New York, NY 10028, USA.
Aristotelis TsirigosDepartment of Pathology, New York University School of Medicine, New York, NY 10016, USA; Applied Bioinformatics Laboratories, NYU School of Medicine, NY 10016, USA.
Matthew CollinInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; Newcastle upon Tyne Hospitals NHS Foundation Trust, Freeman Road, Newcastle upon Tyne NE7 7DN, UK.
Venetia BigleyInstitute of Cellular Medicine, Newcastle University, Newcastle upon Tyne NE2 4HH, UK; Newcastle upon Tyne Hospitals NHS Foundation Trust, Freeman Road, Newcastle upon Tyne NE7 7DN, UK. Electronic address: venetia.bigley@newcastle.ac.uk.
Boris ReizisDepartment of Pathology, New York University School of Medicine, New York, NY 10016, USA; Department of Microbiology and Immunology, Columbia University Medical Center, New York, NY 10032, USA. Electronic address: boris.reizis@nyumc.org.
New York University · USNewcastle University · GBIcahn School of Medicine at Mount Sinai · USColumbia University Irving Medical Center · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Richard Lewis Possemato · 1985 to 2026
$83.1M
PREDOCTORAL TRAINING GRANT IN HUMAN GENETICS &DEVELOPMET32GM007088 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SHEN, MICHAEL M. · 1985 to 2020
$7.1M
ERK control of Dendritic Cell Differentiation, Homeostasis and DiseaseR01CA154947 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CARL E ALLEN, MIRIAM MERAD · 2011 to 2026
$7.0M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR37AI072571 · NIAID · UNIVERSITY OF CHICAGO · PI Boris Reizis · 2018 to 2026
$5.3M
Training Program in Immunology and Inflammation.T32AI100853 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Susan Ruth Schwab · 2012 to 2026
$4.5M
Molecular Control of Plasmacytoid Dendritic Cell Development and FunctionR01AI072571 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2008 to 2017
$4.1M
Harnessing Csf-2 compartmentalized role on tissue resident phagocytes to uncouple anti-tumoral from pathological immunity induced by checkpoint inhibitorsR01CA190400 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MERAD, MIRIAM · 2015 to 2019
$1.9M
Dissecting the aging of hematopoietic stem cells by genetic tracing in vivoR01AG049074 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2015 to 2019
$1.7M
Analyzing dendritic cell development by inducible lineage tracingR21AI115382 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2015 to 2016
$466k
Epigenetic Regulation of Dendritic Cell DevelopmentF31AI124661 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KIRKLING, MARGARET E · 2016 to 2018
$132k
NCI NIH HHS P30 CA016087NCI NIH HHS R01 CA154947NCI NIH HHS R01 CA190400NIAID NIH HHS F31 AI124661NIAID NIH HHS R01 AI072571NIAID NIH HHS R21 AI115382NIAID NIH HHS R37 AI072571NIAID NIH HHS T32 AI100853NIA NIH HHS R01 AG049074NIGMS NIH HHS T32 GM007088Wellcome Trust
6 · The paper itself

Abstract

The IRF8-dependent subset of classical dendritic cells (cDCs), termed cDC1, is important for cross-priming cytotoxic T cell responses against pathogens and tumors. Culture of hematopoietic progenitors with DC growth factor FLT3 ligand (FLT3L) yields very few cDC1s (in humans) or only immature "cDC1-like" cells (in the mouse). We report that OP9 stromal cells expressing the Notch ligand Delta-like 1 (OP9-DL1) optimize FLT3L-driven development of cDC1s from murine immortalized progenitors and primary bone marrow cells. Co-culture with OP9-DL1 induced IRF8-dependent cDC1s with a phenotype (CD103

Indexed as

Cross-PrimingSignal TransductionAnimalsBone Marrow CellsCell DifferentiationCell MovementDendritic CellsHematopoietic Stem CellsHumansMice, Inbred C57BLReceptors, CCR7Receptors, NotchVaccinationReceptors, CCR7Receptors, Notch

Identifiers

PMID29925006
PMCPMC6063084
OpenAlexW2803822216

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.