Evidence map›Paper›PMID 28000664›Full record

ArticleNature communications2016

Endothelial-specific inhibition of NF-κB enhances functional haematopoiesis.

Michael G Poulos, Pradeep Ramalingam, Michael C Gutkin, Maria Kleppe, Michael Ginsberg, Michael J P Crowley, Olivier Elemento, Ross L Levine, Shahin Rafii, Jan Kitajewski and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

37 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  8. The vascular endothelium as decision maker in lung injury.Frontiers in cell and developmental biology · 2025
    Review
  9. Article
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  11. 2Molecular imaging and biology · 2024
    Article
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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

13 authors at 6 institutions in 2 countries.

Michael G PoulosDepartment of Genetic Medicine, Ansary Stem Cell Institute, Weill Cornell Medical College, New York, New York 10021, USA.
Pradeep RamalingamDepartment of Genetic Medicine, Ansary Stem Cell Institute, Weill Cornell Medical College, New York, New York 10021, USA.ORCID http://orcid.org/0000-0002-5943-9670
Michael C GutkinDepartment of Genetic Medicine, Ansary Stem Cell Institute, Weill Cornell Medical College, New York, New York 10021, USA.
Maria KleppeHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Michael GinsbergAngiocrine Bioscience, New York, New York 10065, USA.
Michael J P CrowleyDepartment of Cardiothoracic Surgery, Weill Cornell Medical College, New York, New York 10065, USA.
Olivier ElementoHRH Prince Alwaleed Bin Talal Bin Abdulaziz Al-Saud Institute for Computational Biomedicine, Weill Cornell Medical College, New York, New York 10065, USA.
Ross L LevineHuman Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Shahin RafiiDepartment of Medicine, Division of Regenerative Medicine, Ansary Stem Cell Institute, Weill Cornell Medical College, New York, New York 10065, USA.
Jan KitajewskiDepartment of OB/GYN, Columbia University Medical Center, New York, New York 10032, USA.
Matthew B GreenblattPathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York 10021, USA.
Jae-Hyuck ShimDepartment of Medicine, Division of Rheumatology, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
Jason M ButlerDepartment of Genetic Medicine, Ansary Stem Cell Institute, Weill Cornell Medical College, New York, New York 10021, USA.
Cornell University · USMemorial Sloan Kettering Cancer Center · USAngiocrine Bioscience (United States) · USColumbia University Irving Medical Center · USPrince Sattam Bin Abdulaziz University · SAUniversity of Massachusetts Chan Medical School · US

Funding

Modulation of Bone Formation by SHN3DP5OD021351 · OD · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2015 to 2019
$2.1M
Modulating signaling pathways in endothelial cells to abate leukemic progression.R01CA204308 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BUTLER, JASON MATHEW · 2016 to 2020
$2.0M
"Establishing Pathways for Endothelial Support of Bone Formation with SLIT3"R01AR075585 · NIAMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GREENBLATT, MATTHEW BLAKE · 2020 to 2024
$1.8M
Modulating endothelial-specific signaling to enhance functional hematopoiesis.R01HL133021 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BUTLER, JASON MATHEW · 2016 to 2019
$1.7M
NCI NIH HHS R01 CA204308NHLBI NIH HHS R01 HL133021NIAMS NIH HHS R01 AR075585NIH HHS DP5 OD021351
6 · The paper itself

Abstract

Haematopoietic stem cells (HSCs) reside in distinct niches within the bone marrow (BM) microenvironment, comprised of endothelial cells (ECs) and tightly associated perivascular constituents that regulate haematopoiesis through the expression of paracrine factors. Here we report that the canonical NF-κB pathway in the BM vascular niche is a critical signalling axis that regulates HSC function at steady state and following myelosuppressive insult, in which inhibition of EC NF-κB promotes improved HSC function and pan-haematopoietic recovery. Mice expressing an endothelial-specific dominant negative IκBα cassette under the Tie2 promoter display a marked increase in HSC activity and self-renewal, while promoting the accelerated recovery of haematopoiesis following myelosuppression, in part through protection of the BM microenvironment following radiation and chemotherapeutic-induced insult. Moreover, transplantation of NF-κB-inhibited BM ECs enhanced haematopoietic recovery and protected mice from pancytopenia-induced death. These findings pave the way for development of niche-specific cellular approaches for the treatment of haematological disorders requiring myelosuppressive regimens.

Indexed as

HematopoiesisSignal TransductionAnimalsEndothelial CellsHematopoietic Stem CellsHematopoietic Stem Cell TransplantationMice, Inbred C57BLMice, TransgenicNF-kappa BNF-KappaB Inhibitor alphaPancytopeniaStem Cell NicheNF-kappa BNF-KappaB Inhibitor alpha

Identifiers

PMID28000664
PMCPMC5187502
OpenAlexW2562412556

What OpenQuestion holds

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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.