Evidence map›Paper›PMID 29627966›Full record

ArticleAngiogenesis2018

Spatiotemporal heterogeneity and patterning of developing renal blood vessels.

Edward Daniel, D Berfin Azizoglu, Anne R Ryan, Tezin A Walji, Christopher P Chaney, Gabrielle I Sutton, Thomas J Carroll, Denise K Marciano, Ondine Cleaver

Open access · greenAbstract read
In one paragraph

Article in Angiogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.1field-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

51 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
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  3. Review
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  6. Dynamics of primary cilia in endothelial and mesenchymal cells throughout mouse lung development.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
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  9. Spatial and Temporal Expression Patterns of EDA2R, PCDH9, and TRAF7 inInternational journal of molecular sciences · 2025
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  16. Organoids and tissue/organ chips.Stem cell research & therapy · 2024
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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

9 authors at 2 institutions in 1 country.

Edward DanielDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
D Berfin AzizogluDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Anne R RyanDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Tezin A WaljiDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Christopher P ChaneyDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Gabrielle I SuttonDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Thomas J CarrollDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA.
Denise K MarcianoDepartment of Medicine, Division of Nephrology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Ondine CleaverDepartment of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., NA8.300, Dallas, TX, 75390-9148, USA. ondine.cleaver@utsouthwestern.edu.ORCID 0000-0003-2454-6641
The University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

Engineering erythropoietin-producing cellsR24DK106743 · NIDDK · ROGOSIN INSTITUTE · PI CARROLL, THOMAS JOSEPH, CLEAVER, ONDINE B · 2015 to 2019
$7.0M
Molecular regulation of Rho and Ras family GTPase activity controls vascular lumen formation.R01HL126518 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI CLEAVER, ONDINE B, DAVIS, GEORGE E · 2015 to 2023
$3.1M
Role of afadin signaling in nephron tubulogenesisR01DK099478 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI MARCIANO, DENISE K · 2014 to 2018
$1.7M
Blood vessel tubulogenesis: Rasip1-directed GTPase signaling and cell polarity.R01HL113498 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI CLEAVER, ONDINE B · 2012 to 2015
$1.7M
The role of Wnt signaling in kidney tubule formationR01DK080004 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2008 to 2012
$1.6M
Endothelial Signals During OrganogenesisR01DK079862 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CLEAVER, ONDINE B · 2007 to 2011
$1.5M
Interactions between the stroma and progenitor cells during kidney developmentR01DK095057 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI CARROLL, THOMAS JOSEPH · 2013 to 2016
$1.4M
NHLBI NIH HHS HL113498NHLBI NIH HHS R01 HL113498NHLBI NIH HHS R01 HL126518NIDDK NIH HHS DK079862NIDDK NIH HHS DK080004NIDDK NIH HHS DK095057NIDDK NIH HHS DK099478NIDDK NIH HHS DK106743NIDDK NIH HHS R01 DK079862NIDDK NIH HHS R01 DK080004NIDDK NIH HHS R01 DK095057NIDDK NIH HHS R01 DK099478NIDDK NIH HHS R24 DK106743
6 · The paper itself

Abstract

The kidney vasculature facilitates the excretion of wastes, the dissemination of hormones, and the regulation of blood chemistry. To carry out these diverse functions, the vasculature is regionalized within the kidney and along the nephron. However, when and how endothelial regionalization occurs remains unknown. Here, we examine the developing kidney vasculature to assess its 3-dimensional structure and transcriptional heterogeneity. First, we observe that endothelial cells (ECs) grow coordinately with the kidney bud as early as E10.5, and begin to show signs of specification by E13.5 when the first arteries can be identified. We then focus on how ECs pattern and remodel with respect to the developing nephron and collecting duct epithelia. ECs circumscribe nephron progenitor populations at the distal tips of the ureteric bud (UB) tree and form stereotyped cruciform structures around each tip. Beginning at the renal vesicle (RV) stage, ECs form a continuous plexus around developing nephrons. The endothelial plexus envelops and elaborates with the maturing nephron, becoming preferentially enriched along the early distal tubule. Lastly, we perform transcriptional and immunofluorescent screens to characterize spatiotemporal heterogeneity in the kidney vasculature and identify novel regionally enriched genes. A better understanding of development of the kidney vasculature will help instruct engineering of properly vascularized ex vivo kidneys and evaluate diseased kidneys.

Indexed as

Renal VeinsAnimalsEmbryo, MammalianEndothelial CellsFetal Stem CellsFluorescent Antibody TechniqueKidney Tubules, DistalMiceOrganogenesisRenal ArteryTranscription, GeneticUrethraBlood vesselEndothelial cell heterogeneityEndotheliumEpitheliumNephronVascular patterning

Identifiers

PMID29627966
PMCPMC6491207
OpenAlexW2796286140

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.