Evidence map›Paper›PMID 24767998›Full record

ArticleCell reports2014

Polycystin signaling is required for directed endothelial cell migration and lymphatic development.

Patricia Outeda, David L Huso, Steven A Fisher, Marc K Halushka, Hyunho Kim, Feng Qian, Gregory G Germino, Terry Watnick

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. The endothelium response to kidney injury.Nature reviews. Nephrology · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Cells · 2024
    Article
  8. Article
  9. Review
  10. Molecular Mechanisms Driving Lymphedema and Other Lymphatic Anomalies.Cold Spring Harbor perspectives in medicine · 2022
    Article
  11. Article
  12. Review
  13. The lymphatics in kidney health and disease.Nature reviews. Nephrology · 2021
    Review
  14. Article
  15. Biochemical and mechanical signals in the lymphatic vasculature.Cellular and molecular life sciences : CMLS · 2021
    Review
  16. Review
  17. Review
  18. Article
  19. Recent Progress in Lymphangioma.Frontiers in pediatrics · 2021
    Review
  20. Review
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

8 authors at 3 institutions in 1 country.

Patricia OutedaDivision of Nephrology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
David L HusoDepartment of Molecular and Comparative Pathobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Steven A FisherDivision of Cardiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Marc K HalushkaDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Hyunho KimDivision of Nephrology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Feng QianDivision of Nephrology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Gregory G GerminoNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Terry WatnickDivision of Nephrology, University of Maryland School of Medicine, Baltimore, MD 21201, USA. Electronic address: twatnick@medicine.umaryland.edu.
University of Maryland, Baltimore · USJohns Hopkins Medicine · USNational Institutes of Health · US

Funding

The role of PKD proteins in regulating tubular morphologyZIADK075042 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI GERMINO, GREGORY · 2010 to 2025
$23.3M
Translational Research Enhancement CoreP30DK089502 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI ZACHOS, NICHOLAS CONSTANTINE · 2011 to 2020
$12.0M
Research BaseP30DK090868 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WATNICK, TERRY J · 2010 to 2019
$11.1M
Tissue Hypoxia in Cardiac MorphogenesisR01HL065314 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI FISHER, STEVEN A. · 2000 to 2013
$4.4M
The Proteolytic Cleavage of Polycystin-1: How and WhyR01DK062199 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI QIAN, FENG · 2003 to 2011
$3.1M
Ion Channel Function and Regulation of the Polycystin-1/2 Complex in Kidney Physiology and Polycystic Kidney DiseaseR01DK125404 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI QIAN, FENG, YU, YONG · 2020 to 2024
$2.7M
Novel Approach to the Molecular Genetics of PKD1R37DK048006 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI GERMINO, GREGORY G. · 2004 to 2009
$2.6M
Comprehensive Analysis of Polycystin Related Endothelial Cell Signaling PathwaysR01DK095036 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI WATNICK, TERRY J · 2012 to 2021
$2.3M
PKD1-Fibrillin Interactions and TFG-b Signaling PathwaysR01DK076017 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI WATNICK, TERRY J · 2006 to 2010
$1.5M
Intramural NIH HHS ZIA DK075042NHLBI NIH HHS R01 HL065314NHLBI NIH HHS R01HL65314NIDDK NIH HHS P30 DK089502NIDDK NIH HHS P30 DK090868NIDDK NIH HHS P30DK090868NIDDK NIH HHS R01 DK062199NIDDK NIH HHS R01DK062199NIDDK NIH HHS R01 DK076017NIDDK NIH HHS R01DK076017NIDDK NIH HHS R01 DK095036NIDDK NIH HHS R01DK095036NIDDK NIH HHS R01 DK125404NIDDK NIH HHS R37 DK048006NIDDK NIH HHS R37DK48006PHS HHS 1ZIADK075042
6 · The paper itself

Abstract

Autosomal dominant polycystic kidney disease is a common form of inherited kidney disease that is caused by mutations in two genes, PKD1 (polycystin-1) and PKD2 (polycystin-2). Mice with germline deletion of either gene die in midgestation with a vascular phenotype that includes profound edema. Although an endothelial cell defect has been suspected, the basis of this phenotype remains poorly understood. Here, we demonstrate that edema in Pkd1- and Pkd2-null mice is likely to be caused by defects in lymphatic development. Pkd1 and Pkd2 mutant embryos exhibit reduced lymphatic vessel density and vascular branching along with aberrant migration of early lymphatic endothelial cell precursors. We used cell-based assays to confirm that PKD1- and PKD2-depleted endothelial cells have an intrinsic defect in directional migration that is associated with a failure to establish front-rear polarity. Our studies reveal a role for polycystin signaling in lymphatic development.

Indexed as

Signal TransductionAnimalsCell MovementCell PolarityEmbryo, MammalianEndothelial CellsHumansHuman Umbilical Vein Endothelial CellsLymphatic VesselsLymph NodesMiceMice, Inbred C57BLMice, KnockoutPolycystic Kidney, Autosomal DominantRNA InterferenceRNA, Small InterferingRNA, Small InterferingTRPP Cation Channels

Identifiers

PMID24767998
PMCPMC4040350
OpenAlexW1991969354

What OpenQuestion holds

Textmetadata
LicenceTDM
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.