Evidence map›Paper›PMID 24906860›Full record

ArticleInvestigative ophthalmology & visual science2014

Regulation of intrinsic axon growth ability at retinal ganglion cell growth cones.

Michael B Steketee, Carly Oboudiyat, Richard Daneman, Ephraim Trakhtenberg, Philip Lamoureux, Jessica E Weinstein, Steve Heidemann, Ben A Barres, Jeffrey L Goldberg

Open access · hybridAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The role of mechanics in axonal stability and development.Seminars in cell & developmental biology · 2023
    Review
  6. Article
  7. Article
  8. Transcription factors are potential therapeutic targets in epilepsy.Journal of cellular and molecular medicine · 2022
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Manipulation of Axonal Outgrowth via Exogenous Low Forces.International journal of molecular sciences · 2020
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Axon growth regulation by a bistable molecular switch.Proceedings. Biological sciences · 2018
    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

9 authors at 5 institutions in 1 country.

Michael B SteketeeBascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, United States Department of Ophthalmology and McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States.
Carly OboudiyatBascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, United States.
Richard DanemanDepartment of Neurobiology, Stanford University School of Medicine, Stanford, California, United States.
Ephraim TrakhtenbergBascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, United States.
Philip LamoureuxDepartment of Physiology, Michigan State University, East Lansing, Michigan, United States.
Jessica E WeinsteinBascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, United States.
Steve HeidemannDepartment of Physiology, Michigan State University, East Lansing, Michigan, United States.
Ben A BarresDepartment of Neurobiology, Stanford University School of Medicine, Stanford, California, United States.
Jeffrey L GoldbergBascom Palmer Eye Institute and Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, Florida, United States Department of Ophthalmology, Shiley Eye Center, University of California San Diego, San Diego, California, United States.
University of Miami · USStanford University · USMcGowan Institute for Regenerative Medicine · USMichigan State University · USMichigan United · US

Funding

Shared Equipment ModuleP30EY014801 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Victor L Perez · 2004 to 2026
$12.2M
Vision BiostatisticsP30EY022589 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Derek Stuart Welsbie · 2012 to 2026
$10.3M
REPAIR AND REGENERATION OF CENTRAL VISUAL PATHWAYSR01EY011310 · NEI · STANFORD UNIVERSITY · PI BARRES, BEN A · 1996 to 2014
$4.7M
Kruppel-like Transcription Factors in Retinal Ganglion Cell RegenerationR01EY020913 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GOLDBERG, JEFFREY L · 2010 to 2013
$2.2M
Synapses,Channels, and Transduction in NeuroscienceT32NS007044 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI MULLER, KENNETH J · 1985 to 2010
$2.2M
NEI NIH HHS P30 EY014801NEI NIH HHS P30-EY014801NEI NIH HHS P30 EY022589NEI NIH HHS P30-EY022589NEI NIH HHS R01 EY011310NEI NIH HHS R01-EY011310NEI NIH HHS R01 EY020913NEI NIH HHS R01-EY020913NINDS NIH HHS T32 NS007044NINDS NIH HHS T32-NS007044
6 · The paper itself

Abstract

purposeMammalian central nervous system neurons fail to regenerate after injury or disease, in part due to a progressive loss in intrinsic axon growth ability after birth. Whether lost axon growth ability is due to limited growth resources or to changes in the axonal growth cone is unknown.

methodsStatic and time-lapse images of purified retinal ganglion cells (RGCs) were analyzed for axon growth rate and growth cone morphology and dynamics without treatment and after manipulating Kruppel-like transcription factor (KLF) expression or applying mechanical tension.

resultsRetinal ganglion cells undergo a developmental switch in growth cone dynamics that mirrors the decline in postnatal axon growth rates, with increased filopodial adhesion and decreased lamellar protrusion area in postnatal axonal growth cones. Moreover, expressing growth-suppressive KLF4 or growth-enhancing KLF6 transcription factors elicits similar changes in postnatal growth cones that correlate with axon growth rates. Postnatal RGC axon growth rate is not limited by an inability to achieve axon growth rates similar to embryonic RGCs; indeed, postnatal axons support elongation rates up to 100-fold faster than postnatal axonal growth rates. Rather, the intrinsic capacity for rapid axon growth is due to both growth cone pausing and retraction, as well as to a slightly decreased ability to achieve rapid instantaneous rates of forward progression. Finally, we observed that RGC axon and dendrite growth are regulated independently in vitro.

conclusionsTogether, these data support the hypothesis that intrinsic axon growth rate is regulated by an axon-specific growth program that differentially regulates growth cone motility.

Indexed as

AnimalsAnimals, NewbornAxonsCell ProliferationDisease Models, AnimalFemaleGrowth ConesKruppel-Like Factor 4MaleNerve RegenerationNeuronsOptic NerveRatsRats, Sprague-DawleyRetinal DiseasesRetinal Ganglion CellsKruppel-Like Factor 4axonCNSfilopodiagrowth coneKLFlamellipodiaregeneration

Identifiers

PMID24906860
PMCPMC4102390
OpenAlexW1979545053

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.