Evidence map›Paper›PMID 18666204›Full record

ArticleDevelopmental neurobiology2008

Mitochondrial biogenesis in the axons of vertebrate peripheral neurons.

Mandana Amiri, Peter J Hollenbeck

Open access · greenAbstract read
In one paragraph

Article in Developmental neurobiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

100 citing papers in PubMed, 163 citations in OpenAlex.

  1. FASEB bioAdvances · 2026
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  13. Axonal mitophagy in retinal ganglion cells.Cell communication and signaling : CCS · 2024
    Review
  14. Article
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  16. A detailed review of pharmacology of MFN1 (mitofusion-1)-mediated mitochondrial dynamics: Implications for cellular health and diseases.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
    Review
  17. Review
  18. Review
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  20. Review

40 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.

Mandana AmiriDepartment of Biological Sciences, Purdue University, West Lafayette, Indiana 47906, USA.
Peter J Hollenbeck
Purdue University West Lafayette · US

Funding

CONTROL OF NEURONAL ORGANELLE TRANSPORTR01NS027073 · NINDS · PURDUE UNIVERSITY WEST LAFAYETTE · PI HOLLENBECK, PETER J. · 1990 to 2013
$3.6M
Control of Neural Organelle TransportR56NS027073 · NINDS · PURDUE UNIVERSITY · PI HOLLENBECK, PETER J. · 2009 to 2009
$374k
NINDS NIH HHS NS027073NINDS NIH HHS R01 NS027073NINDS NIH HHS R56 NS027073
6 · The paper itself

Abstract

Mitochondria are widely distributed via regulated transport in neurons, but their sites of biogenesis remain uncertain. Most mitochondrial proteins are encoded in the nuclear genome, and evidence has suggested that mitochondrial DNA (mtDNA) replication occurs mainly or entirely in the cell body. However, it has also become clear that nuclear-encoded mitochondrial proteins can be translated in the axon and that components of the mitochondrial replication machinery reside there as well. We assessed directly whether mtDNA replication can occur in the axons of chick peripheral neurons labeled with 5-bromo-2'-deoxyuridine (BrdU). In axons that were physically separated from the cell body or had disrupted organelle transport between the cell bodies and axons, a significant fraction of mtDNA synthesis continued. We also detected the mitochondrial fission protein Drp1 in neurons by immunofluorescence or expression of GFP-Drp1. Its presence and distribution on the majority of axonal mitochondria indicated that a substantial number had undergone recent division in the axon. Because the morphology of mitochondria is maintained by the balance of fission and fusion events, we either inhibited Drp1 expression by RNAi or overexpressed the fusion protein Mfn1. Both methods resulted in significantly longer mitochondria in axons, including many at a great distance from the cell body. These data indicate that mitochondria can replicate their DNA, divide, and fuse locally within the axon; thus, the biogenesis of mitochondria is not limited to the cell body.

Indexed as

AnimalsAxonsBromodeoxyuridineCells, CulturedChick EmbryoDNA, MitochondrialDNA ReplicationDynaminsFluorescent Antibody TechniqueGanglia, SpinalGanglia, SympatheticGene Expression Regulation, DevelopmentalMitochondriaNeurogenesisPeripheral Nervous SystemBromodeoxyuridineDNA, MitochondrialDnm1l protein, ratDynamins

Identifiers

PMID18666204
PMCPMC2538952
OpenAlexW2060031105

What OpenQuestion holds

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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.