Evidence map›Paper›PMID 25605896›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Intracellular and extracellular forces drive primary cilia movement.

Christopher Battle, Carolyn M Ott, Dylan T Burnette, Jennifer Lippincott-Schwartz, Christoph F Schmidt

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
5.2field-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

35 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Broadening horizons: Pathogenesis and therapeutics of renal ciliopathies.Journal of cell communication and signaling · 2026
    Review
  3. Article
  4. Article
  5. Lab on an end: Micromanipulation using the acoustohydrodynamic pillar array as an end effector.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. The dynamics of tubulogenesis in development and disease.Development (Cambridge, England) · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Rediscovering Primary Cilia in Pancreatic Islets.Diabetes & metabolism journal · 2023
    Review
  13. Scanning electron microscopy of human islet cilia.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Fluorescence imaging of beta cell primary cilia.Frontiers in endocrinology · 2022
    Article
  18. Article
  19. Article
  20. 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 4 institutions in 2 countries.

Christopher BattleDrittes Physikalisches Institut, Georg-August-Universität, 37077 Göttingen, Germany;
Carolyn M OttEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892; and.
Dylan T BurnetteDepartment of Cell and Developmental Biology, Vanderbilt Medical Center, Nashville, TN 37232.
Jennifer Lippincott-SchwartzEunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892; and lippincj@mail.nih.gov cfs@physik3.gwdg.de.
Christoph F SchmidtDrittes Physikalisches Institut, Georg-August-Universität, 37077 Göttingen, Germany; lippincj@mail.nih.gov cfs@physik3.gwdg.de.
University of Göttingen · DEEunice Kennedy Shriver National Institute of Child Health and Human Development · USNational Institutes of Health · USVanderbilt University Medical Center · US

Funding

Organization and Dynamics of Endomembrane Pathways and OrganellesZIAHD001609 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BONIFACINO, JUAN · 2009 to 2019
$16.2M
Intramural NIH HHS
6 · The paper itself

Abstract

Primary cilia are ubiquitous, microtubule-based organelles that play diverse roles in sensory transduction in many eukaryotic cells. They interrogate the cellular environment through chemosensing, osmosensing, and mechanosensing using receptors and ion channels in the ciliary membrane. Little is known about the mechanical and structural properties of the cilium and how these properties contribute to ciliary perception. We probed the mechanical responses of primary cilia from kidney epithelial cells [Madin-Darby canine kidney-II (MDCK-II)], which sense fluid flow in renal ducts. We found that, on manipulation with an optical trap, cilia deflect by bending along their length and pivoting around an effective hinge located below the basal body. The calculated bending rigidity indicates weak microtubule doublet coupling. Primary cilia of MDCK cells lack interdoublet dynein motors. Nevertheless, we found that the organelles display active motility. 3D tracking showed correlated fluctuations of the cilium and basal body. These angular movements seemed random but were dependent on ATP and cytoplasmic myosin-II in the cell cortex. We conclude that force generation by the actin cytoskeleton surrounding the basal body results in active ciliary movement. We speculate that actin-driven ciliary movement might tune and calibrate ciliary sensory functions.

Indexed as

MovementAnimalsCentrosomeCiliaDogsMadin Darby Canine Kidney CellsMicroscopy, Electronactive fluctuationsciliary motilityflexural rigiditymechanosensingprimary cilium

Identifiers

PMID25605896
PMCPMC4321243
OpenAlexW1966164668

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.