Evidence map›Paper›PMID 29773667›Full record

ArticleScience (New York, N.Y.)2018

Notch ligand Dll1 mediates cross-talk between mammary stem cells and the macrophageal niche.

Rumela Chakrabarti, Toni Celià-Terrassa, Sushil Kumar, Xiang Hang, Yong Wei, Abrar Choudhury, Julie Hwang, Jia Peng, Briana Nixon, John J Grady and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
9.1field-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

115 citing papers in PubMed, 196 citations in OpenAlex.

  1. Review
  2. Article
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  6. Nuclei sense complex tissue shape and direct intestinal stem cell fate.bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
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  11. Review
  12. Article
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  14. CXCR4Nature communications · 2025
    Article
  15. Article
  16. Review
  17. Review
  18. Review
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  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 2 countries.

Rumela ChakrabartiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. ykang@princeton.edu rumela@vet.upenn.edu.ORCID 0000-0003-2124-8737
Toni Celià-TerrassaDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-0615-8744
Sushil KumarDepartment of Biomedical Sciences, University of Pennsylvania, Philadelphia, PA 19104, USA.
Xiang HangDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Yong WeiDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0002-1034-649X
Abrar ChoudhuryDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Julie HwangDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0003-3779-5129
Jia PengDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
Briana NixonImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
John J GradyDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0001-6684-7958
Christina DeCosteDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.ORCID 0000-0003-4002-0244
Jie GaoDepartment of Pathology, NYU Langone Medical Center, New York City, NY 10016, USA.ORCID 0000-0002-0955-4435
Johan H van EsHubrecht Institute and University Medical Center Utrecht, Utrecht, Netherlands.
Ming O LiImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.ORCID 0000-0002-1383-0535
Iannis AifantisDepartment of Pathology, NYU Langone Medical Center, New York City, NY 10016, USA.ORCID 0000-0001-6857-1035
Hans CleversDepartment of Pathology, NYU Langone Medical Center, New York City, NY 10016, USA.ORCID 0000-0002-3077-5582
Yibin KangDepartment of Molecular Biology, Princeton University, Princeton, NJ 08544, USA. ykang@princeton.edu rumela@vet.upenn.edu.ORCID 0000-0002-1626-6730
Princeton University · USNYU Langone Health · USMemorial Sloan Kettering Cancer Center · USRutgers, The State University of New Jersey · USUniversity Medical Center Utrecht · NLUniversity of Pennsylvania · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TRANSCRIPTIONAL PROFILINGP30CA072720 · NCI · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Chang S Chan · 1997 to 2026
$94.5M
Ontogeny and Function of Tumor-associated MacrophagesR01CA198280 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI LI, MING · 2015 to 2019
$2.3M
The Role of miRNAs in Epithelial-Mesenchymal Transition and MetastasisR01CA141062 · NCI · PRINCETON UNIVERSITY · PI KANG, YIBIN · 2010 to 2014
$1.6M
Probing the role of tumor suppressive functions of Elf5 in breast cancerK22CA193661 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CHAKRABARTI, RUMELA · 2016 to 2018
$562k
Examining the Role of IRF8 in Tumor-Associated Macrophage Differentiation and FunctionF31CA210332 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI NIXON, BRIANA GLYN · 2017 to 2019
$134k
NCI NIH HHS F31 CA210332NCI NIH HHS K22 CA193661NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA072720NCI NIH HHS R01 CA141062NCI NIH HHS R01 CA198280
6 · The paper itself

Abstract

The stem cell niche is a specialized environment that dictates stem cell function during development and homeostasis. We show that Dll1, a Notch pathway ligand, is enriched in mammary gland stem cells (MaSCs) and mediates critical interactions with stromal macrophages in the surrounding niche in mouse models. Conditional deletion of Dll1 reduced the number of MaSCs and impaired ductal morphogenesis in the mammary gland. Moreover, MaSC-expressed Dll1 activates Notch signaling in stromal macrophages, increasing their expression of Wnt family ligands such as Wnt3, Wnt10A, and Wnt16, thereby initiating a feedback loop that promotes the function of Dll1-expressing MaSCs. Together, these findings reveal functionally important cross-talk between MaSCs and their macrophageal niche through Dll1-mediated Notch signaling.

Indexed as

AnimalsCalcium-Binding ProteinsCell CountFemaleGene Knockout TechniquesIntercellular Signaling Peptides and ProteinsLigandsMacrophagesMammary Glands, AnimalMiceMice, KnockoutMorphogenesisReceptors, NotchSignal TransductionStem Cell NicheStem CellsCalcium-Binding ProteinsDlk1 protein, mouseIntercellular Signaling Peptides and ProteinsLigandsReceptors, NotchWnt Proteins

Identifiers

PMID29773667
PMCPMC7881440
OpenAlexW2804505252

What OpenQuestion holds

Textmetadata
LicenceTDM
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.