Evidence map›Paper›PMID 25894677›Full record

ArticleNeurochemical research2015

Fine Astrocyte Processes Contain Very Small Mitochondria: Glial Oxidative Capability May Fuel Transmitter Metabolism.

Amin Derouiche, Julia Haseleu, Horst-Werner Korf

Abstract read
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In one paragraph

Article in Neurochemical research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed.

  1. Context-Dependent modulation of astrocytic CaJournal of computational neuroscience · 2026
    Article
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  7. Astrocytic pathology in Alpers' syndrome.Acta neuropathologica communications · 2023
    Article
  8. Article
  9. How expensive is the astrocyte?Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Article
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  15. Review
  16. Review
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  18. Review
  19. Physiology of Astroglial Excitability.Function (Oxford, England) · 2020
    Article
  20. 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

3 authors.

Amin DerouicheDr. Senckenbergische Anatomie, Institut für Anatomie II, Goethe-Universität, Frankfurt am Main, Germany. Derouiche@em.uni-frankfurt.de.
Julia HaseleuInstitute of Cellular Neurosciences, University of Bonn, Bonn, Germany.
Horst-Werner KorfDr. Senckenbergische Anatomie, Institut für Anatomie II, Goethe-Universität, Frankfurt am Main, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The peripheral astrocyte process (PAP) is the glial compartment largely handling inactivation of transmitter glutamate, and supplying glutamate to the axon terminal. It is not clear how these energy demanding processes are fueled, and whether the PAP exhibits oxidative capability. Whereas the GFAP-positive perinuclear cytoplasm and stem process are rich in mitochondria, the PAP is often considered too narrow to contain mitochondria and might thus not rely on oxidative metabolism. Applying high resolution light microscopy, we investigate here the presence of mitochondria in the PAPs of freshly dissociated, isolated astrocytes. We provide an overview of the subcellular distribution and the approximate size of astrocytic mitochondria. A substantial proportion of the astrocyte's mitochondria are contained in the PAPs and, on the average, they are smaller there than in the stem processes. The majority of mitochondria in the stem and peripheral processes are surprisingly small (0.2-0.4 µm), spherical and not elongate, or tubular, which is supported by electron microscopy. The density of mitochondria is two to several times lower in the PAPs than in the stem processes. Thus, PAPs do not constitute a mitochondria free glial compartment but contain mitochondria in large numbers. No juxtaposition of mitochondria-containing PAPs and glutamatergic synapses has been reported. However, the issue of sufficient ATP concentrations in perisynaptic PAPs can be seen in the light of (1) the rapid, activity dependent PAP motility, and (2) the recently reported activity-dependent mitochondrial transport and immobilization leading to spatial, subcellular organisation of glutamate uptake and oxidative metabolism.

Indexed as

Adenosine TriphosphateAnimalsAstrocytesGlial Fibrillary Acidic ProteinMitochondriaMitochondrial SizeNeural Stem CellsNeurogliaNeurotransmitter AgentsOxidation-ReductionPeripheral Nervous SystemPrimary Cell CultureRatsSubcellular FractionsSynapsesAdenosine TriphosphateGlial Fibrillary Acidic ProteinNeurotransmitter AgentsEzrinGlia-synaptic interactionMetabolic compartmentationPAPsUltrastructure

Identifiers

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Read underepoch 390

Registered trials

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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.