Evidence map›Paper›PMID 23819925›Full record

ArticleCilia2013

An inducible CiliaGFP mouse model for in vivo visualization and analysis of cilia in live tissue.

Amber K O'Connor, Erik B Malarkey, Nicolas F Berbari, Mandy J Croyle, Courtney J Haycraft, P Darwin Bell, Peter Hohenstein, Robert A Kesterson, Bradley K Yoder

Open access · bronzeAbstract read
In one paragraph

Article in Cilia, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

56 citing papers in PubMed, 82 citations in OpenAlex.

  1. Primary cilia: sensors of biliary homeostasis and disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Paracrine Signaling by Pancreatic Islet Cilia.Current opinion in endocrine and metabolic research · 2024
    Article
  10. Article
  11. Review
  12. Rediscovering Primary Cilia in Pancreatic Islets.Diabetes & metabolism journal · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Fluorescence imaging of beta cell primary cilia.Frontiers in endocrinology · 2022
    Article
  17. Islet cilia and glucose homeostasis.Frontiers in cell and developmental biology · 2022
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Amber K O'Connor *6Center for Translational Science, Children's National Medical Center, Washington, DC 20010, USA.
Erik B Malarkey *1Department of Cell, Development, and Integrative Biology, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
Nicolas F Berbari1Department of Cell, Development, and Integrative Biology, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
Mandy J Croyle1Department of Cell, Development, and Integrative Biology, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
Courtney J HaycraftDepartment of Craniofacial Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
P Darwin BellRalph H. Johnson Veterans Administration Medical Center, Department of Medicine, Division of Nephrology, Medical University of South Carolina, Charleston, SC 29425, USA.
Peter HohensteinThe Roslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian Scotland, UK.
Robert A Kesterson5Department of Genetics, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
Bradley K Yoder1Department of Cell, Development, and Integrative Biology, University of Alabama at Birmingham Medical School, Birmingham, AL 35294, USA.
University of Alabama at Birmingham · USMedical University of South Carolina · USChildren's National · USUniversity of Edinburgh · GB

Funding

UAB Recessive PKD Research and Translational Core CenterP30DK074038 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YODER, BRADLEY K. · 2005 to 2019
$16.6M
ROS Modulation of Innate and Adaptive Immunity in RAP30AR048311 · NIAMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MOUNTZ, JOHN D · 2001 to 2017
$9.5M
Cilia and Cystic Kidney DiseaseR01DK065655 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI YODER, BRADLEY K. · 2004 to 2017
$4.4M
NIAMS NIH HHS P30 AR048311NIDDK NIH HHS P30 DK074038NIDDK NIH HHS R01 DK065655
6 · The paper itself

Abstract

backgroundCilia are found on nearly every cell type in the mammalian body, and have been historically classified as either motile or immotile. Motile cilia are important for fluid and cellular movement; however, the roles of non-motile or primary cilia in most tissues remain unknown. Several genetic syndromes, called the ciliopathies, are associated with defects in cilia structure or function and have a wide range of clinical presentations. Much of what we know about the formation and maintenance of cilia comes from model systems like C. elegans and Chalmydomonas. Studies of mammalian cilia in live tissues have been hampered by difficulty visualizing them.

resultsTo facilitate analyses of mammalian cilia function we generated an inducible CiliaGFP mouse by targeting mouse cDNA encoding a cilia-localized protein somatostatin receptor 3 fused to GFP (Sstr3::GFP) into the ROSA26 locus. In this system, Sstr3::GFP is expressed from the ubiquitous ROSA26 promoter after Cre mediated deletion of an upstream Neo cassette flanked by lox P sites. Fluorescent cilia labeling was observed in a variety of live tissues and after fixation. Both cell-type specific and temporally regulated cilia labeling were obtained using multiple Cre lines. The analysis of renal cilia in anesthetized live mice demonstrates that cilia commonly lay nearly parallel to the apical surface of the tubule. In contrast, in more deeply anesthetized mice the cilia display a synchronized, repetitive oscillation that ceases upon death, suggesting a relationship to heart beat, blood pressure or glomerular filtration.

conclusionsThe ability to visualize cilia in live samples within the CiliaGFP mouse will greatly aid studies of ciliary function. This mouse will be useful for in vivo genetic and pharmacological screens to assess pathways regulating cilia motility, signaling, assembly, trafficking, resorption and length control and to study cilia regulated physiology in relation to ciliopathy phenotypes.

Identifiers

PMID23819925
PMCPMC3700774
OpenAlexW2144542308

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.