Evidence map›Paper›PMID 26844267›Full record

ArticleEBioMedicine2015

Muscle A-Kinase Anchoring Protein-α is an Injury-Specific Signaling Scaffold Required for Neurotrophic- and Cyclic Adenosine Monophosphate-Mediated Survival.

Yan Wang, Evan G Cameron, Jinliang Li, Travis L Stiles, Michael D Kritzer, Rahul Lodhavia, Jonathan Hertz, Tu Nguyen, Michael S Kapiloff, Jeffrey L Goldberg

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

25 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Adenylyl Cyclases as Therapeutic Targets in Neuroregeneration.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Exploring AKAPs in visual signaling.Frontiers in molecular neuroscience · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Quantitative BONCAT Allows Identification of Newly Synthesized Proteins after Optic Nerve Injury.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Regulation of Neuronal Survival and Axon Growth by a Perinuclear cAMP Compartment.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    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

10 authors at 3 institutions in 1 country.

Yan WangBascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, United States; Department of Ophthalmology, University of California, San Diego, CA 92093, United States.
Evan G CameronDepartment of Ophthalmology, University of California, San Diego, CA 92093, United States; Byers Eye Institute, Stanford University, Palo Alto, CA 94303, United States.
Jinliang LiDepartment of Pediatrics, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States; Department of Medicine, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States.
Travis L StilesDepartment of Ophthalmology, University of California, San Diego, CA 92093, United States.
Michael D KritzerDepartment of Pediatrics, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States; Department of Medicine, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States.
Rahul LodhaviaDepartment of Ophthalmology, University of California, San Diego, CA 92093, United States.
Jonathan HertzBascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, United States.
Tu NguyenDepartment of Ophthalmology, University of California, San Diego, CA 92093, United States.
Michael S KapiloffDepartment of Pediatrics, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States; Department of Medicine, Interdisciplinary Stem Cell Institute, Leonard M. Miller School of Medicine, University of Miami, Miami, FL, 33136, United States.
Jeffrey L GoldbergBascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL 33136, United States; Department of Ophthalmology, University of California, San Diego, CA 92093, United States; Byers Eye Institute, Stanford University, Palo Alto, CA 94303, United States.
University of Miami · USUniversity of California, San Diego · USSmith-Kettlewell Eye Research Institute · US

Funding

Vision BiostatisticsP30EY022589 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Derek Stuart Welsbie · 2012 to 2026
$10.3M
Signaling Scaffolds and Survival in StrokeR01EY022129 · NEI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI GOLDBERG, JEFFREY L, KAPILOFF, MICHAEL SETH · 2012 to 2015
$2.3M
NEI NIH HHS P30 EY022589NEI NIH HHS P30-EY022589NEI NIH HHS R01 EY022129NEI NIH HHS R01-EY022129
6 · The paper itself

Abstract

Neurotrophic factor and cAMP-dependent signaling promote the survival and neurite outgrowth of retinal ganglion cells (RGCs) after injury. However, the mechanisms conferring neuroprotection and neuroregeneration downstream to these signals are unclear. We now reveal that the scaffold protein muscle A-kinase anchoring protein-α (mAKAPα) is required for the survival and axon growth of cultured primary RGCs. Although genetic deletion of mAKAPα early in prenatal RGC development did not affect RGC survival into adulthood, nor promoted the death of RGCs in the uninjured adult retina, loss of mAKAPα in the adult increased RGC death after optic nerve crush. Importantly, mAKAPα was required for the neuroprotective effects of brain-derived neurotrophic factor and cyclic adenosine-monophosphate (cAMP) after injury. These results identify mAKAPα as a scaffold for signaling in the stressed neuron that is required for RGC neuroprotection after optic nerve injury.

Indexed as

Signal TransductionA Kinase Anchor ProteinsAnimalsCell SurvivalCyclic AMPFemaleGene ExpressionGene Knockout TechniquesMaleMiceMice, KnockoutNerve Growth FactorsNeuritesOptic Nerve InjuriesRatsRats, TransgenicAkap6 protein, ratA Kinase Anchor ProteinsCyclic AMPNerve Growth FactorsAxon growthmAKAPOptic nerve injuryRetinal ganglion cellsSurvival

Identifiers

PMID26844267
PMCPMC4703706
OpenAlexW1867393201

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.