Evidence map›Paper›PMID 27050519›Full record

ArticleCell reports2016

Evidence for an Age-Dependent Decline in Axon Regeneration in the Adult Mammalian Central Nervous System.

Cédric G Geoffroy, Brett J Hilton, Wolfram Tetzlaff, Binhai Zheng

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

90 citing papers in PubMed, 159 citations in OpenAlex.

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  12. Hyperactive delta isoform of PI3 kinase enables long-distance regeneration of adult rat corticospinal tract.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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30 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

4 authors at 3 institutions in 2 countries.

Cédric G GeoffroyDepartment of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0691, USA.
Brett J HiltonInternational Collaboration on Repair Discoveries, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada; Department of Zoology, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Wolfram TetzlaffInternational Collaboration on Repair Discoveries, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada; Department of Zoology, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada; Department of Surgery, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada. Electronic address: tetzlaff@icord.org.
Binhai ZhengDepartment of Neurosciences, School of Medicine, University of California, San Diego, La Jolla, CA 92093-0691, USA. Electronic address: binhai@ucsd.edu.
University of California San Diego · USInternational Collaboration On Repair Discoveries · CAUniversity of British Columbia · CA

Funding

U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
TRAINING IN THE NEUROPLASTICITY OF AGINGT32AG000216 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KOO, EDWARD H. · 1992 to 2017
$8.4M
The Role of a Pair of MAP3Ks in the Multicellular Response to Spinal Cord InjuryR01NS093055 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHENG, BINHAI · 2015 to 2024
$4.0M
Genetic analysis of myelin inhibitors and PTEN in injury-inducedCNS axon growthR01NS054734 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHENG, BINHAI · 2007 to 2015
$3.2M
Canadian Institutes of Health ResearchNIA NIH HHS T32 AG000216NIA NIH HHS T32AG000216NINDS NIH HHS P30 NS047101NINDS NIH HHS R01 NS054734NINDS NIH HHS R01NS054734NINDS NIH HHS R01 NS093055NINDS NIH HHS R01NS093055
6 · The paper itself

Abstract

How aging impacts axon regeneration after CNS injury is not known. We assessed the impact of age on axon regeneration induced by Pten deletion in corticospinal and rubrospinal neurons, two neuronal populations with distinct innate regenerative abilities. As in young mice, Pten deletion in older mice remains effective in preventing axotomy-induced decline in neuron-intrinsic growth state, as assessed by mTOR activity, neuronal soma size, and axonal growth proximal to a spinal cord injury. However, axonal regeneration distal to injury is greatly diminished, accompanied by increased expression of astroglial and inflammatory markers at the injury site. Thus, the mammalian CNS undergoes an age-dependent decline in axon regeneration, as revealed when neuron-intrinsic growth state is elevated. These results have important implications for developing strategies to promote axonal repair after CNS injuries or diseases, which increasingly affect middle-aged to aging populations.

Indexed as

Nerve RegenerationAgingAnimalsAstrocytesAxonsAxotomyBiomarkersCentral Nervous SystemDown-RegulationGene DeletionInflammationMammalsMicePTEN PhosphohydrolasePyramidal TractsSignal TransductionBiomarkersPTEN PhosphohydrolaseTOR Serine-Threonine Kinases

Identifiers

PMID27050519
PMCPMC5050004
OpenAlexW2319017449

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.