Evidence map›Paper›PMID 24578264›Full record

ArticleDevelopmental neurobiology2014

Activation of PI3K and R-Ras signaling promotes the extension of sensory axons on inhibitory chondroitin sulfate proteoglycans.

Lee Silver, James V Michael, Lawrence E Goldfinger, Gianluca Gallo

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The Axonal Glycolytic Pathway Contributes to Sensory Axon Extension and Growth Cone Dynamics.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Avian axons undergo Wallerian degeneration after injury and stress.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2016
    Article
  13. Article
  14. Review
  15. Article
  16. 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

4 authors at 3 institutions in 1 country.

Lee SilverDepartment of Anatomy and Cell Biology, Temple University School of Medicine, 3500 North Broad St., Philadelphia, Pennsylvania, 19140; Shriners Hospitals Pediatric Research Center, Temple University School of Medicine, Philadelphia, Pennsylvania, 19140.
James V Michael
Lawrence E Goldfinger
Gianluca Gallo
Temple University · USFox Chase Cancer Center · USTemple University Hospital · US

Funding

R-Ras signaling in vascular biologyR01HL093416 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI GOLDFINGER, LAWRENCE E · 2010 to 2014
$1.9M
Localized translation of cytoskeletal proteins in axonal morphogenesisR01NS078030 · NINDS · TEMPLE UNIV OF THE COMMONWEALTH · PI GALLO, GIANLUCA · 2013 to 2017
$1.7M
NHLBI NIH HHS HL093416NHLBI NIH HHS R01 HL093416NINDS NIH HHS NS078030NINDS NIH HHS R01 NS078030
6 · The paper itself

Abstract

Chondroitin sulfate proteoglycans (CSPGs) are extracellular inhibitors of axon extension and plasticity, and cause growth cones to exhibit dystrophic behaviors. Phosphoinositide 3-kinase (PI3K) is a lipid kinase activated by axon growth promoting signals. In this study, we used embryonic chicken dorsal root ganglion neurons to determine if CSPGs impair signaling through PI3K. We report that CSPGs inhibit PI3K signaling in axons and growth cones, as evidenced by decreased levels of phosphorylated downstream kinases (Akt and S6). Direct activation of PI3K signaling, using a cell permeable phosphopeptide (PI3Kpep), countered the effects of CSPGs on growth cones and axon extension. Both overnight and acute treatment with PI3Kpep promoted axon extension on CSPG-coated substrates. The R-Ras GTPase is an upstream positive regulator of PI3K signaling. Expression of constitutively active R-Ras promoted axon extension and growth cone elaboration on CSPGs and permissive substrata. In contrast, an N-terminus-deleted constitutively active R-Ras, deficient in PI3K activation, promoted axon extension but not growth cone elaboration on CSPGs and permissive substrata. These data indicate that activation of R-Ras-PI3K signaling may be a viable approach for manipulating axon extension on CSPGs.

Indexed as

AnimalsAvian ProteinsAxonsCell Culture TechniquesChick EmbryoChondroitin Sulfate ProteoglycansGanglia, SpinalGrowth ConesPhosphatidylinositol 3-KinasesPhosphorylationProto-Oncogene Proteins c-aktras ProteinsRibosomal Protein S6 KinasesSensory Receptor CellsSignal TransductionTissue Culture TechniquesAvian ProteinsChondroitin Sulfate ProteoglycansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktras ProteinsRibosomal Protein S6 KinasesAktgrowth coneneuriteregenerationS6

Identifiers

PMID24578264
PMCPMC4235675
OpenAlexW2137690131

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.