Evidence map›Paper›PMID 32348770›Full record

ArticleCell reports2020

Id1 and Id3 Maintain Steady-State Hematopoiesis by Promoting Sinusoidal Endothelial Cell Survival and Regeneration.

Stephen Gadomski, Satyendra K Singh, Shweta Singh, Tanmoy Sarkar, Kimberly D Klarmann, Maximillian Berenschot, Steven Seaman, Brad Jakubison, Kristbjorn O Gudmundsson, Stephen Lockett and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

21 citing papers in PubMed, 26 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

11 authors at 4 institutions in 1 country.

Stephen GadomskiMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Satyendra K SinghMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Shweta SinghMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Tanmoy SarkarMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Kimberly D KlarmannMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Maximillian BerenschotMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Steven SeamanMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA.
Brad JakubisonMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Kristbjorn O GudmundssonMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Stephen LockettOptical Microscopy and Analysis Laboratory, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Jonathan R KellerMouse Cancer Genetics Program, Center for Cancer Research, NCI, Frederick, MD 21702, USA; Basic Science Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. Electronic address: kellerjo@mail.nih.gov.
Cancer Genetics (United States) · USCenter for Cancer Research · USFrederick National Laboratory for Cancer Research · USLeidos (United States) · US

Funding

Molecular-Cellular Regulation of Hematopoietic Stem CellsZIABC010001 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KELLER, JONATHAN R · 2009 to 2024
$16.8M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS ZIA BC010001NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Investigating mechanisms that regulate endothelial cell (EC) growth and survival is important for understanding EC homeostasis and how ECs maintain stem cell niches. We report here that targeted loss of Id genes in adult ECs results in dilated, leaky sinusoids and a pro-inflammatory state that increases in severity over time. Disruption in sinusoidal integrity leads to increased hematopoietic stem cell (HSC) proliferation, differentiation, migration, and exhaustion. Mechanistically, sinusoidal ECs (SECs) show increased apoptosis because of reduced Bcl2-family gene expression following Id gene ablation. Furthermore, Id1

Indexed as

AnimalsCell SurvivalDisease Models, AnimalEndothelial CellsFemaleHematopoiesisHumansInhibitor of Differentiation Protein 1Inhibitor of Differentiation ProteinsMaleMiceMice, Inbred C57BLRegenerationIdb1 protein, mouseIdb3 protein, mouseInhibitor of Differentiation Protein 1Inhibitor of Differentiation Proteinsbone marrowendothelial cellshematopoietic microenvironmenthematopoietic stem cellsID proteinsinstructive nicheprogenitor cellsproliferationtissue regenerationtranscription factors

Identifiers

PMID32348770
PMCPMC8459380
OpenAlexW3018617564

What OpenQuestion holds

Textmetadata
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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.