Evidence map›Paper›PMID 31039135›Full record

ArticleThe Journal of clinical investigation2019

Bone marrow dendritic cells regulate hematopoietic stem/progenitor cell trafficking.

Jingzhu Zhang, Teerawit Supakorndej, Joseph R Krambs, Mahil Rao, Grazia Abou-Ezzi, Rachel Y Ye, Sidan Li, Kathryn Trinkaus, Daniel C Link

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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 56 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Jingzhu ZhangDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Teerawit SupakorndejDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Joseph R KrambsDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Mahil RaoDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Grazia Abou-EzziDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Rachel Y YeDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Sidan LiDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Kathryn TrinkausBiostatistics Shared Resource, Siteman Cancer Center, Washington University School of Medicine, Saint Louis, Missouri, USA.
Daniel C LinkDivision of Oncology, Department of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Washington University in St. Louis · USCapital Medical University · CNJewish Hospital · US

Funding

Specimen Acquistition and Expression ProfilingP01CA101937 · NCI · WASHINGTON UNIVERSITY · PI LEY, TIMOTHY J. · 2003 to 2023
$58.8M
6 · The paper itself

Abstract

A resident population of dendritic cells (DCs) has been identified in murine bone marrow, but its contribution to the regulation of hematopoiesis and establishment of the stem cell niche is largely unknown. Here, we show that murine bone marrow DCs are perivascular and have a type 2 conventional DC (cDC2) immunophenotype. RNA expression analysis of sorted bone marrow DCs shows that expression of many chemokines and chemokine receptors is distinct from that observed in splenic cDC2s, suggesting that bone marrow DCs may represent a unique DC population. A similar population of DCs is present in human bone marrow. Ablation of conventional DCs (cDCs) results in hematopoietic stem/progenitor cell (HSPC) mobilization that is greater than that seen with ablation of bone marrow macrophages, and cDC ablation also synergizes with G-CSF to mobilize HSPCs. Ablation of cDCs is associated with an expansion of bone marrow endothelial cells and increased vascular permeability. CXCR2 expression in sinusoidal endothelial cells and the expression of two CXCR2 ligands, CXCL1 and CXCL2, in the bone marrow are markedly increased following cDC ablation. Treatment of endothelial cells in vitro with CXCL1 induces increased vascular permeability and HSPC transmigration. Finally, we show that HSPC mobilization after cDC ablation is attenuated in mice lacking CXCR2 expression. Collectively, these data suggest that bone marrow DCs play an important role in regulating HSPC trafficking, in part, through regulation of sinusoidal CXCR2 signaling and vascular permeability.

Indexed as

Capillary PermeabilityCell MovementSignal TransductionAnimalsBone Marrow CellsChemokine CXCL1Chemokine CXCL2Dendritic CellsHematopoietic Stem CellsHumansMiceMice, KnockoutReceptors, Interleukin-8BChemokine CXCL1Chemokine CXCL2Cxcl1 protein, mouseCxcl2 protein, mouseReceptors, Interleukin-8BBone marrowDendritic cellsHematologyHematopoietic stem cellsStem cells

Identifiers

PMID31039135
PMCPMC6597218
OpenAlexW2943724803

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.