Evidence map›Paper›PMID 19229553›Full record

ReviewHistochemistry and cell biology2009

Degradation of excess peroxisomes in mammalian liver cells by autophagy and other mechanisms.

Sadaki Yokota, H Dariush Fahimi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Histochemistry and cell biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
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  3. Article
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  8. Article
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  11. The cell biology of the retinal pigment epithelium.Progress in retinal and eye research · 2020
    Review
  12. Pexophagy: A Model for Selective Autophagy.International journal of molecular sciences · 2020
    Review
  13. Diverse Functions of Autophagy in Liver Physiology and Liver Diseases.International journal of molecular sciences · 2019
    Review
  14. Article
  15. Pexophagy in yeast and mammals: an update on mysteries.Histochemistry and cell biology · 2018
    Review
  16. Review
  17. Article
  18. Article
  19. Peroxisomes and Kidney Injury.Antioxidants & redox signaling · 2016
    Review
  20. Review
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 2 institutions in 2 countries.

Sadaki YokotaSection of Functional Morphology, Faculty of Pharmaceutical Sciences, Nagasaki International University, Huis Ten Bosch 2825-7, Sasebo, Nagasaki 859-3298, Japan. syokota@niu.ac.jp
H Dariush Fahimi
Heidelberg University · DENagasaki International University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we discuss the mechanisms for the degradation of excess peroxisomes in mammalian hepatocytes which include (a) autophagy, (b) the action of peroxisomal Lon protease and (c) the membrane disrupting effect of 15-lipoxygenase. A recent study using Atg7 conditional-knock-out mice revealed that 70-80% of excess peroxisomes are degraded by the autophagic process. The remaining 20-30% of excess peroxisomes is most probably degraded by the action of peroxisomal Lon protease. Finally, a selective disruption of the peroxisomal membrane has been shown to be mediated by 15-lipoxygenase activity which is followed by diffusion of matrix proteins into the cytoplasm and cytoplasmic proteolysis.

Indexed as

AnimalsArachidonate 15-LipoxygenaseAutophagyCytoplasmHepatocytesIntracellular MembranesMicePeroxisomesProtease LaArachidonate 15-LipoxygenaseProtease La

Identifiers

PMID19229553
OpenAlexW2001341803

What OpenQuestion holds

Textmetadata
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.