Evidence map›Paper›PMID 31107242›Full record

ArticleThe Journal of clinical investigation2019

Secreted nuclear protein DEK regulates hematopoiesis through CXCR2 signaling.

Maegan L Capitano, Nirit Mor-Vaknin, Anjan K Saha, Scott Cooper, Maureen Legendre, Haihong Guo, Rafael Contreras-Galindo, Ferdinand Kappes, Maureen A Sartor, Christopher T Lee and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Clinicopathological insights and prognostic implications of DEK in association with apoptosis-regulating factors in ovarian cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 3 countries.

Maegan L CapitanoDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Nirit Mor-VakninDepartment of Internal Medicine, Division of Infectious Disease, University of Michigan, Ann Arbor, Michigan, USA.
Anjan K SahaDepartment of Internal Medicine, Division of Infectious Disease, University of Michigan, Ann Arbor, Michigan, USA.
Scott CooperDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Maureen LegendreDepartment of Internal Medicine, Division of Infectious Disease, University of Michigan, Ann Arbor, Michigan, USA.
Haihong GuoInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, Aachen, Germany.
Rafael Contreras-GalindoDepartment of Internal Medicine, Division of Infectious Disease, University of Michigan, Ann Arbor, Michigan, USA.
Ferdinand KappesInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, Aachen, Germany.
Maureen A SartorDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, USA.
Christopher T LeeDepartment of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
Xinxin HuangDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
David M MarkovitzDepartment of Internal Medicine, Division of Infectious Disease, University of Michigan, Ann Arbor, Michigan, USA.
Hal E BroxmeyerDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
University of Michigan · USIndiana University School of MedicineRWTH Aachen University · DEXi’an Jiaotong-Liverpool University · CN

Funding

Project-005U54DK106846 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Reuben Kapur, Karen Elizabeth Pollok · 2015 to 2026
$9.7M
REGULATION OF HEMATOPOIETIC CELL PRODUCTIONT32DK007519 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KAPLAN, MARK H · 1986 to 2020
$7.1M
MECHANISMS OF SYNERGISTIC REGULATION OF STEM/PROGENITORSR01HL056416 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI BROXMEYER, HAL E. · 1996 to 2017
$6.0M
Enhancing Engraftment of Cord Blood by CD26 InhibitionR01HL112669 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI BROXMEYER, HAL E., FARAG, SHERIF S · 2012 to 2016
$3.6M
Controlling Influences of Oxygen Tension and CD26/DPP4 Enzymatic Activity on Regulation of Hematopoietic Stem/Progenitor Cells and Hematopoiesis During Health, Ageing, and DiseaseR35HL139599 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI BROXMEYER, HAL E. · 2018 to 2021
$3.1M
DEK Regulation of Hematopoietic Stem Cell Renewal, Fate, and HematopoiesisR01DK109188 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI BROXMEYER, HAL E., MARKOVITZ, DAVID MICHAEL · 2016 to 2019
$2.0M
The Role of Centromeres in the Molecular Biology of Prostate CancerF30CA210379 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SAHA, ANJAN KUMAR · 2016 to 2018
$119k
NCI NIH HHS F30 CA210379NHLBI NIH HHS R01 HL056416NHLBI NIH HHS R01 HL112669NHLBI NIH HHS R35 HL139599NIDDK NIH HHS R01 DK109188NIDDK NIH HHS T32 DK007519NIDDK NIH HHS U54 DK106846
6 · The paper itself

Abstract

The nuclear protein DEK is an endogenous DNA-binding chromatin factor regulating hematopoiesis. DEK is one of only 2 known secreted nuclear chromatin factors, but whether and how extracellular DEK regulates hematopoiesis is not known. We demonstrated that extracellular DEK greatly enhanced ex vivo expansion of cytokine-stimulated human and mouse hematopoietic stem cells (HSCs) and regulated HSC and hematopoietic progenitor cell (HPC) numbers in vivo and in vitro as determined both phenotypically (by flow cytometry) and functionally (through transplantation and colony formation assays). Recombinant DEK increased long-term HSC numbers and decreased HPC numbers through a mechanism mediated by the CXC chemokine receptor CXCR2 and heparan sulfate proteoglycans (HSPGs) (as determined utilizing Cxcr2-/- mice, blocking CXCR2 antibodies, and 3 different HSPG inhibitors) that was associated with enhanced phosphorylation of ERK1/2, AKT, and p38 MAPK. To determine whether extracellular DEK required nuclear function to regulate hematopoiesis, we utilized 2 mutant forms of DEK: one that lacked its nuclear translocation signal and one that lacked DNA-binding ability. Both altered HSC and HPC numbers in vivo or in vitro, suggesting the nuclear function of DEK is not required. Thus, DEK acts as a hematopoietic cytokine, with the potential for clinical applicability.

Indexed as

HematopoiesisMAP Kinase Signaling SystemAnimalsChromosomal Proteins, Non-HistoneCytokinesDNA-Binding ProteinsExtracellular Signal-Regulated MAP KinasesHematopoietic Stem CellsHumansMiceMice, KnockoutMutationOncogene ProteinsPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-aktRats, Sprague-DawleyChromosomal Proteins, Non-HistoneCXCR2 protein, humanCytokinesDEK protein, humanDEK protein, mouseDNA-Binding ProteinsExtracellular Signal-Regulated MAP KinasesOncogene ProteinsPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-aktReceptors, Interleukin-8BChemokinesHematologyHematopoietic stem cellsStem cells

Identifiers

PMID31107242
PMCPMC6546479
OpenAlexW2944894501

What OpenQuestion holds

Textmetadata
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.