Evidence map›Paper›PMID 28846069›Full record

ArticleThe Journal of clinical investigation2017

Secreted protein Del-1 regulates myelopoiesis in the hematopoietic stem cell niche.

Ioannis Mitroulis, Lan-Sun Chen, Rashim Pal Singh, Ioannis Kourtzelis, Matina Economopoulou, Tetsuhiro Kajikawa, Maria Troullinaki, Athanasios Ziogas, Klara Ruppova, Kavita Hosur and 14 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
–field-weighted citation impact
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

64 citing papers in PubMed.

  1. DEL-1 is an Endogenous Senolytic Protein that Inhibits Senescence-Associated Bone Loss.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. 3DACS biomaterials science & engineering · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Emergency myelopoiesis in solid cancers.British journal of haematology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. The role of secreted proteins in efferocytosis.Frontiers in cell and developmental biology · 2023
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Bone Marrow Niches of Hematopoietic Stem and Progenitor Cells.International journal of molecular sciences · 2022
    Review
  20. Molecular regulation of hematopoietic stem cell quiescence.Cellular and molecular life sciences : CMLS · 2022
    Review

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

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Ioannis MitroulisDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Lan-Sun ChenDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Rashim Pal SinghDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Ioannis KourtzelisDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Matina EconomopoulouDepartment of Ophthalmology, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Tetsuhiro KajikawaDepartment of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Maria TroullinakiDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Athanasios ZiogasDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Klara RuppovaDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Kavita HosurDepartment of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Tomoki MaekawaDepartment of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Baomei WangDepartment of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Pallavi SubramanianDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Torsten TonnInstitute for Transfusion Medicine, German Red Cross Blood Donation Service North-East, Dresden, Germany.
Panayotis VerginisDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Malte von BoninMedical Clinic and Policlinic I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Manja WobusMedical Clinic and Policlinic I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Martin BornhäuserMedical Clinic and Policlinic I, University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Tatyana GrinenkoDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
Marianna Di ScalaArea of Cell and Developmental Biology, Fundación Centro Nacional de Investigaciones Cardiovasculares (CNIC) Carlos III, Madrid, Spain.
Andres HidalgoArea of Cell and Developmental Biology, Fundación Centro Nacional de Investigaciones Cardiovasculares (CNIC) Carlos III, Madrid, Spain.
Ben WielockxDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.
George HajishengallisDepartment of Microbiology, Penn Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Triantafyllos ChavakisDepartment of Clinical Pathobiochemistry, Institute for Clinical Chemistry and Laboratory Medicine, and.

Funding

Role of complement in kidney disorders: from hemodialysis to transportationP01AI068730 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI LAMBRIS, JOHN D · 2007 to 2018
$16.0M
P. gingivalis as a keystone pathogenR01DE015254 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI HAJISHENGALLIS, GEORGIOS · 2004 to 2018
$4.6M
Local endogenous regulators of functional immune plasticity in the periodontiumR37DE026152 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI HAJISHENGALLIS, GEORGIOS · 2016 to 2025
$3.5M
Neutrophil homeostasis and periodontitis: Novel concepts and treatmentsR01DE024153 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI HAJISHENGALLIS, GEORGIOS · 2016 to 2020
$2.0M
Del-1: Molecular and Cellular Targets in PeriodontitisR01DE024716 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI HAJISHENGALLIS, GEORGIOS · 2015 to 2019
$2.0M
NIAID NIH HHS P01 AI068730NIDCR NIH HHS R01 DE015254NIDCR NIH HHS R01 DE024153NIDCR NIH HHS R01 DE024716NIDCR NIH HHS R37 DE026152
6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs) remain mostly quiescent under steady-state conditions but switch to a proliferative state following hematopoietic stress, e.g., bone marrow (BM) injury, transplantation, or systemic infection and inflammation. The homeostatic balance between quiescence, self-renewal, and differentiation of HSCs is strongly dependent on their interactions with cells that constitute a specialized microanatomical environment in the BM known as the HSC niche. Here, we identified the secreted extracellular matrix protein Del-1 as a component and regulator of the HSC niche. Specifically, we found that Del-1 was expressed by several cellular components of the HSC niche, including arteriolar endothelial cells, CXCL12-abundant reticular (CAR) cells, and cells of the osteoblastic lineage. Del-1 promoted critical functions of the HSC niche, as it regulated long-term HSC (LT-HSC) proliferation and differentiation toward the myeloid lineage. Del-1 deficiency in mice resulted in reduced LT-HSC proliferation and infringed preferentially upon myelopoiesis under both steady-state and stressful conditions, such as hematopoietic cell transplantation and G-CSF- or inflammation-induced stress myelopoiesis. Del-1-induced HSC proliferation and myeloid lineage commitment were mediated by β3 integrin on hematopoietic progenitors. This hitherto unknown Del-1 function in the HSC niche represents a juxtacrine homeostatic adaptation of the hematopoietic system in stress myelopoiesis.

Indexed as

MyelopoiesisStem Cell NicheStress, PhysiologicalAnimalsCalcium-Binding ProteinsCarrier ProteinsCell Adhesion MoleculesChemokine CXCL12Endothelial CellsHematopoietic Stem CellsHumansIntegrin beta3Intercellular Signaling Peptides and ProteinsMiceMice, KnockoutCalcium-Binding ProteinsCarrier ProteinsCell Adhesion MoleculesChemokine CXCL12CXCL12 protein, humanCxcl12 protein, mouseEDIL3 protein, humanEdil3 protein, mouseIntegrin beta3Intercellular Signaling Peptides and ProteinsITGB3 protein, human

Identifiers

PMID28846069
PMCPMC5617665

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.