Evidence map›Paper›PMID 20937270›Full record

ArticleDevelopmental biology2011

Developmental ablation of Id1 and Id3 genes in the vasculature leads to postnatal cardiac phenotypes.

Qingshi Zhao, Amanda J Beck, Joseph M Vitale, Joel S Schneider, Shumin Gao, Corey Chang, Genie Elson, Samuel J Leibovich, Ji Yeon Park, Bin Tian and 2 more

Abstract read
In one paragraph

Article in Developmental biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Single-cell RNA sequencing reveals thatThe European respiratory journal · 2022
    Article
  5. Article
  6. Hearing Loss in Id1Frontiers in genetics · 2021
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Developmental and pathological angiogenesis in the central nervous system.Cellular and molecular life sciences : CMLS · 2014
    Review
  15. Article
  16. Article
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

12 authors at 2 institutions in 1 country.

Qingshi ZhaoDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, UMDNJ, Newark, NJ 07107-1709, USA.
Amanda J Beck
Joseph M Vitale
Joel S Schneider
Shumin Gao
Corey Chang
Genie Elson
Samuel J Leibovich
Ji Yeon Park
Bin Tian
Hyung-song Nam
Diego Fraidenraich
Memorial Sloan Kettering Cancer Center · USRutgers, The State University of New Jersey · US

Funding

Toll-Like Receptors, Adenosine and AngiogenesisR01GM068636 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LEIBOVICH, SAMUEL JOSEPH · 2003 to 2011
$3.3M
Role of Id genes during cardiac developmentK01HL076568 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FRAIDENRAICH, DIEGO · 2004 to 2008
$667k
Role of murine induced pluripotent stem cells on the correction of cardiac and skR21HL094905 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI FRAIDENRAICH, DIEGO · 2009 to 2010
$429k
Alternative mRNA processing in cardiac hypertrophyR21HL098802 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI TIAN, BIN · 2010 to 2011
$429k
NHLBI NIH HHS HL076568NHLBI NIH HHS HL094905NHLBI NIH HHS HL098802NHLBI NIH HHS K01 HL076568NHLBI NIH HHS R21 HL094905NHLBI NIH HHS R21 HL098802NIGMS NIH HHS GM068636NIGMS NIH HHS R01 GM068636
6 · The paper itself

Abstract

The Id1 and Id3 genes play major roles during cardiac development, despite their expression being confined to non-myocardial layers (endocardium-endothelium-epicardium). We previously described that Id1Id3 double knockout (dKO) mouse embryos die at mid-gestation from multiple cardiac defects, but early lethality precluded the studies of the roles of Id in the postnatal heart. To elucidate postnatal roles of Id genes, we ablated the Id3 gene and conditionally ablated the Id1 gene in the endothelium to generate conditional KO (cKO) embryos. We observed cardiac phenotypes at birth and at 6 months of age. Half of the Id cKO mice died at birth. Postnatal demise was associated with cardiac enlargement and defects in the ventricular septum, trabeculation and vasculature. Surviving Id cKO mice exhibited fibrotic vasculature, cardiac enlargement and decreased cardiac function. An abnormal vascular response was also observed in the healing of excisional skin wounds of Id cKO mice. Expression patterns of vascular, fibrotic and hypertrophic markers were altered in the Id cKO hearts, but addition of Insulin-Like Growth Factor binding protein-3 (IGFbp3) reversed gene expression profiles of vascular and fibrotic, but not hypertrophic markers. Thus, ablation of Id genes in the vasculature leads to distinct postnatal cardiac phenotypes. These findings provide important insights into the role/s of the endocardial network of the endothelial lineage in the development of cardiac disease, and highlight IGFbp3 as a potential link between Id and its vascular effectors.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBiomarkersCell LineageEndothelial CellsGene Expression ProfilingHeart DiseasesInhibitor of Differentiation Protein 1Inhibitor of Differentiation ProteinsInsulin-Like Growth Factor Binding Protein 3MiceMice, KnockoutMyocardiumPhenotypeWound HealingBiomarkersIdb1 protein, mouseIdb3 protein, mouseInhibitor of Differentiation Protein 1Inhibitor of Differentiation ProteinsInsulin-Like Growth Factor Binding Protein 3

Identifiers

PMID20937270
PMCPMC2993814
OpenAlexW1994446256

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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.