Evidence map›Paper›PMID 17761534›Full record

ArticleMolecular biology of the cell2007

ErbB4 isoforms selectively regulate growth factor induced Madin-Darby canine kidney cell tubulogenesis.

Fenghua Zeng, Ming-Zhi Zhang, Amar B Singh, Roy Zent, Raymond C Harris

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. ErbB4 deletion predisposes to development of metabolic syndrome in mice.American journal of physiology. Endocrinology and metabolism · 2018
    Article
  6. Article
  7. ErbB4 deletion accelerates renal fibrosis following renal injury.American journal of physiology. Renal physiology · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Receptor tyrosine kinases in the nucleus.Cold Spring Harbor perspectives in biology · 2013
    Review
  18. Epidermal growth factors in the kidney and relationship to hypertension.American journal of physiology. Renal physiology · 2013
    Review
  19. Article
  20. ErbB4 modulates tubular cell polarity and lumen diameter during kidney development.Journal of the American Society of Nephrology : JASN · 2012
    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

5 authors at 1 institution in 1 country.

Fenghua ZengDepartment of Medicine, Vanderbilt University, Nashville, TN 37232, USA.
Ming-Zhi Zhang
Amar B Singh
Roy Zent
Raymond C Harris
Vanderbilt University · US

Funding

The Role of the EGF Receptor in Acute and Chronic Renal InjuryR01DK051265 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RAYMOND C. HARRIS, Mingzhi Zhang · 1997 to 2026
$10.1M
The Laminin Receptors in Kidney FibrosisR01DK069921 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ROY ZENT · 2005 to 2026
$9.5M
NIDDK NIH HHS DK69921NIDDK NIH HHS R01 DK051265NIDDK NIH HHS R01 DK069921
6 · The paper itself

Abstract

ErbB4, a member of the epidermal growth factor (EGF) receptor family that can be activated by heregulin beta1 and heparin binding (HB)-EGF, is expressed as alternatively spliced isoforms characterized by variant extracellular juxtamembrane (JM) and intracellular cytoplasmic (CYT) domains. ErbB4 plays a critical role in cardiac and neural development. We demonstrated that ErbB4 is expressed in the ureteric buds and developing tubules of embryonic rat kidney and in collecting ducts in adult. The predominant isoforms expressed in kidney are JM-a and CYT-2. In ErbB4-transfected MDCK II cells, basal cell proliferation and hepatocyte growth factor (HGF)-induced tubule formation were decreased by all four isoforms. Only JM-a/CYT-2 cells formed tubules upon HB-EGF stimulation. ErbB4 was activated by both HRG-beta1 and HB-EGF stimulation; however, compared with HRG-beta1, HB-EGF induced phosphorylation of the 80-kDa cytoplasmic cleavage fragment of the JM-a/CYT-2 isoform. HB-EGF also induced early activation of ERK1/2 in JM-a/CYT-2 cells and promoted nuclear translocation of the JM-a/CYT-2 cytoplasmic tail. In summary, our data indicate that JM-a/CYT-2, the ErbB4 isoform that is proteinase cleavable but does not contain a PI3K-binding domain in its cytoplasmic tail, mediates important functions in renal epithelial cells in response to HB-EGF.

Indexed as

Active Transport, Cell NucleusAgingAmino Acid SequenceAnimalsCell AdhesionCell DifferentiationCell LineCell ProliferationCollagen Type IDogsErbB ReceptorsGene Expression RegulationHeparin-binding EGF-like Growth FactorHumansIntercellular Signaling Peptides and ProteinsIsoenzymesCollagen Type IERBB4 protein, humanErbb4 protein, ratErbB ReceptorsHBEGF protein, humanHbegf protein, ratHeparin-binding EGF-like Growth FactorIntercellular Signaling Peptides and ProteinsIsoenzymesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Neuregulin-1Receptor, ErbB-4

Identifiers

PMID17761534
PMCPMC2043549
OpenAlexW2158699923

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.