Evidence map›Paper›PMID 20615870›Full record

ArticleThe Journal of biological chemistry2010

Mammalian target of rapamycin (mTOR) activation increases axonal growth capacity of injured peripheral nerves.

Namiko Abe, Steven H Borson, Michael J Gambello, Fan Wang, Valeria Cavalli

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed
4.6field-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

139 citing papers in PubMed, 214 citations in OpenAlex.

  1. Development of aBioactive materials · 2026
    Article
  2. Article
  3. Article
  4. Balancing inflammation and regeneration: immune cell dynamics in nerve repair: a comprehensive review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Disruption of G3BP1 granules promotes mammalian CNS and PNS axon regeneration.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Positive Effects of Argon Inhalation After Traumatic Brain Injury in Rats.International journal of molecular sciences · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Unleashing Intrinsic Growth Pathways in Regenerating Peripheral Neurons.International journal of molecular sciences · 2022
    Review
  19. Review
  20. Article

79 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Namiko AbeDepartment of Anatomy and Neurobiology, Washington University in St. Louis, School of Medicine, St. Louis, Missouri 63110, USA.
Steven H Borson
Michael J Gambello
Fan Wang
Valeria Cavalli
Washington University in St. Louis · USDuke University · USThe University of Texas Health Science Center at Houston · US

Funding

MECHANISMS REGULATING VESICULAR AXONAL TRANSPORT FOLLOWING NERVE INJURYR01NS060709 · NINDS · WASHINGTON UNIVERSITY · PI CAVALLI, VALERIA · 2008 to 2011
$1.3M
NINDS NIH HHS R01 NS060709NINDS NIH HHS R01NS060709
6 · The paper itself

Abstract

Unlike neurons in the central nervous system (CNS), injured neurons in the peripheral nervous system (PNS) can regenerate their axons and reinnervate their targets. However, functional recovery in the PNS often remains suboptimal, especially in cases of severe damage. The lack of regenerative ability of CNS neurons has been linked to down-regulation of the mTOR (mammalian target of rapamycin) pathway. We report here that PNS dorsal root ganglial neurons (DRGs) activate mTOR following damage and that this activity enhances axonal growth capacity. Furthermore, genetic up-regulation of mTOR activity by deletion of tuberous sclerosis complex 2 (TSC2) in DRGs is sufficient to enhance axonal growth capacity in vitro and in vivo. We further show that mTOR activity is linked to the expression of GAP-43, a crucial component of axonal outgrowth. However, although TSC2 deletion in DRGs facilitates axonal regrowth, it leads to defects in target innervation. Thus, whereas manipulation of mTOR activity could provide new strategies to stimulate nerve regeneration in the PNS, fine control of mTOR activity is required for proper target innervation.

Indexed as

Peripheral Nerve InjuriesAnimalsAxonsFemaleGanglia, SpinalGAP-43 ProteinGene DeletionGene Expression RegulationHumansIntracellular Signaling Peptides and ProteinsMicePeripheral NervesProtein Serine-Threonine KinasesRecovery of FunctionRegenerationTOR Serine-Threonine KinasesGAP-43 ProteinIntracellular Signaling Peptides and ProteinsMTOR protein, humanmTOR protein, mouseProtein Serine-Threonine KinasesTOR Serine-Threonine KinasesTSC2 protein, humanTsc2 protein, mouseTuberous Sclerosis Complex 2 ProteinTumor Suppressor Proteins

Identifiers

PMID20615870
PMCPMC2934668
OpenAlexW2091285282

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.