Evidence map›Paper›PMID 27493873›Full record

ArticleJournal of cachexia, sarcopenia and muscle2016

p62/SQSTM1 but not LC3 is accumulated in sarcopenic muscle of mice.

Kunihiro Sakuma, Masakazu Kinoshita, Yoshinori Ito, Miki Aizawa, Wataru Aoi, Akihiko Yamaguchi

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Review
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  7. iScience · 2024
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  14. Role of mitophagy in the hallmarks of aging.Journal of biomedical research · 2022
    Article
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  16. Article
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  19. Mitochondrial Dynamics and Mitophagy in Skeletal Muscle Health and Aging.International journal of molecular sciences · 2021
    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

6 authors.

Kunihiro SakumaResearch Center for Physical Fitness, Sports and Health Toyohashi University of Technology Toyohashi, 1-1 Hibarigaoka, Tenpaku-cho 441-8580 Japan.
Masakazu KinoshitaResearch Center for Physical Fitness, Sports and Health Toyohashi University of Technology Toyohashi, 1-1 Hibarigaoka, Tenpaku-cho 441-8580 Japan.
Yoshinori ItoResearch Center for Physical Fitness, Sports and Health Toyohashi University of Technology Toyohashi, 1-1 Hibarigaoka, Tenpaku-cho 441-8580 Japan.
Miki AizawaResearch Center for Physical Fitness, Sports and Health Toyohashi University of Technology Toyohashi, 1-1 Hibarigaoka, Tenpaku-cho 441-8580 Japan.
Wataru AoiLaboratory of Health Science, Graduate School of Life and Environmental Sciences Kyoto Prefectural University Kyoto Japan.
Akihiko YamaguchiDepartment of Physical Therapy Health Sciences University of Hokkaido Kanazawa Ishikari-Tobetsu, Hokkaido Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimWe investigated the pathway of autophagy signaling linked to sarcopenia of mice.

methodsYoung adult (3-month) and aged (24- month) C57BL/6J mice were used. Using real-time PCR, Western blotting, and immunohistochemical microscopy, we evaluated the amounts of p62/SQSTM1, LC3, and Beclin-1 in the quadriceps muscle change with aging in mice.

resultsMarked fiber atrophy (30%) and many fibers with central nuclei were observed in the aged mice. Western blotting using homogenate of the cytosolic fraction clearly showed that the amounts of p62/SQSTM1 and Beclin-1 proteins were significantly increased in the aged skeletal muscle. The amounts of these proteins in both nuclear and membrane fractions did not change significantly with age. Immunofluorescence labeling indicated that aged mice more frequently possessed p62/SQSTM1-positive fibers in the cytosol in quadriceps muscle than young ones (aged: 14% vs. young: 1%). In aged muscle, p62/SQSTM1-positive fibers were significantly smaller than the surrounding p62/SQSTM1-negative fibers. Aging did not elicit significant changes in the mRNA levels of p62/SQSTM1 and Beclin-1, but decreased LC3 mRNA level. In aged muscle, the location of p62/SQSTM1 immunoreactivity was similar to that of Beclin-1 protein, but not LC3.

conclusionSarcopenia in mice appears to include a marked defect of autophagy signaling.

Indexed as

AtrophyLC3, Beclin‐1p62/SQSTM1SarcopeniaSkeletal muscle

Identifiers

PMID27493873
PMCPMC4864138

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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.