Evidence map›Paper›PMID 22049414›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

PKA/AKAP1 and PP2A/Bβ2 regulate neuronal morphogenesis via Drp1 phosphorylation and mitochondrial bioenergetics.

Audrey S Dickey, Stefan Strack

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

133 citing papers in PubMed, 197 citations in OpenAlex.

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  11. bioRxiv : the preprint server for biology · 2025
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  12. Review
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  14. Review
  15. DRP1, fission and apoptosis.Cell death discovery · 2025
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

73 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

2 authors at 1 institution in 1 country.

Audrey S DickeyDepartment of Pharmacology and Neuroscience Graduate Program, University of Iowa, Iowa City, Iowa 52242, USA.
Stefan Strack
University of Iowa · US

Funding

Kinase/Phosphatase-mediated Mitochondrial Restructuring in NeuroprotectionR01NS056244 · NINDS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2007 to 2016
$2.9M
Regulatory Subunits of PP2A in Neuronal FunctionR01NS043254 · NINDS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2003 to 2011
$2.9M
Regulation of Mitochondrial Fission/Fusion by PP2A and PKA in NeuronsR01NS057714 · NINDS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2007 to 2009
$594k
Kinase/phosphatase-mediated Mitochondrial Restructuring in NeuroprotectionR56NS056244 · NINDS · UNIVERSITY OF IOWA · PI STRACK, STEFAN · 2012 to 2012
$378k
NINDS NIH HHS NS043254NINDS NIH HHS NS056244NINDS NIH HHS NS057714NINDS NIH HHS R01 NS043254NINDS NIH HHS R01 NS056244NINDS NIH HHS R01 NS057714NINDS NIH HHS R56 NS056244
6 · The paper itself

Abstract

Mitochondrial shape is determined by fission and fusion reactions, perturbation of which can contribute to neuronal injury and disease. Mitochondrial fission is catalyzed by dynamin-related protein 1 (Drp1), a large GTPase of the dynamin family that is highly expressed in neurons and regulated by various posttranslational modifications, including phosphorylation. We report here that reversible phosphorylation of Drp1 at a conserved Ser residue by an outer mitochondrial kinase (PKA/AKAP1) and phosphatase (PP2A/Bβ2) impacts dendrite and synapse development in cultured rat hippocampal neurons. PKA/AKAP1-mediated phosphorylation of Drp1 at Ser656 increased mitochondrial length and dendrite occupancy, enhancing dendritic outgrowth but paradoxically decreasing synapse number and density. Opposing PKA/AKAP1, PP2A/Bβ2-mediated dephosphorylation of Drp1 at Ser656 fragmented and depolarized mitochondria and depleted them from dendrites, stunting dendritic outgrowth but augmenting synapse formation. Raising and lowering intracellular calcium reproduced the effects of dephospho-Drp1 and phospho-Drp1on dendrite and synapse development, respectively, while boosting mitochondrial membrane potential with l-carnitine-fostered dendrite at the expense of synapse formation without altering mitochondrial size or distribution. Thus, outer mitochondrial PKA and PP2A regulate neuronal development by inhibiting and promoting mitochondrial division, respectively. We propose that the bioenergetic state of mitochondria, rather than their localization or shape per se, is the key effector of Drp1, altering calcium homeostasis to modulate neuronal morphology and connectivity.

Indexed as

A Kinase Anchor ProteinsAnalysis of VarianceAnimalsCarnitineCyclic AMP-Dependent Protein KinasesDendritesDynaminsEmbryo, MammalianEnergy MetabolismExcitatory Amino Acid AntagonistsGreen Fluorescent ProteinsHippocampusMembrane Potential, MitochondrialMembrane Transport ProteinsMicroscopy, ConfocalMitochondria2-amino-5-phosphopentanoic acidAkap1 protein, ratA Kinase Anchor ProteinsCarnitineCyclic AMP-Dependent Protein KinasesDnm1l protein, ratDynaminsExcitatory Amino Acid AntagonistsGreen Fluorescent ProteinsMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsMitochondrial ProteinsNerve Tissue ProteinsProtein Phosphatase 2Receptors, Cell SurfaceReceptors, Cytoplasmic and NuclearSodium Channel BlockersTetrodotoxinTomm20 protein, ratValineVesicular Transport Proteins

Identifiers

PMID22049414
PMCPMC3328351
OpenAlexW1967744942

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.