Evidence map›Paper›PMID 30133343›Full record

ArticleMolecular biology of the cell2018

Spatial regulation of the actin cytoskeleton by HSF-1 during aging.

Ryo Higuchi-Sanabria, Joseph W Paul, Jenni Durieux, Camila Benitez, Phillip A Frankino, Sarah U Tronnes, Gilberto Garcia, Joseph R Daniele, Samira Monshietehadi, Andrew Dillin

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

41 citing papers in PubMed, 61 citations in OpenAlex.

  1. More than the 'master regulator of cytosolic proteostasis': new roles for HSF1 in promoting tissue health.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Alterations of actin in aging.Journal of cell science · 2026
    Review
  6. Article
  7. Form and function of actin impacts actin health and aging.bioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Imaging actin organisation and dynamics in 3D.Journal of cell science · 2024
    Article
  18. Article
  19. Overexpression of Lifeact in theFrontiers in cell and developmental biology · 2024
    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

10 authors at 1 institution in 1 country.

Ryo Higuchi-SanabriaDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Joseph W PaulDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Jenni DurieuxDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Camila BenitezDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Phillip A FrankinoDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Sarah U TronnesDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Gilberto GarciaDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Joseph R DanieleDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Samira MonshietehadiDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Andrew DillinDepartment of Molecular and Cell Biology, Howard Hughes Medical Institute, and.
Howard Hughes Medical Institute · US

Funding

The Collapse of Proteostasis during Aging is Mediated by Cytoskeletal Actin FunctionsR01AG055891 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI DILLIN, ANDREW G · 2017 to 2021
$1.6M
The Cytoskeletal Stress Response: A Novel Facet to Protecting Cell Integrity during AgingF32AG053023 · NIA · UNIVERSITY OF CALIFORNIA BERKELEY · PI HIGUCHI-SANABRIA, RYO · 2016 to 2018
$168k
Howard Hughes Medical InstituteNIA NIH HHS F32 AG053023NIA NIH HHS R01 AG055891
6 · The paper itself

Abstract

There are many studies suggesting an age-associated decline in the actin cytoskeleton, and this has been adopted as common knowledge in the field of aging biology. However, a direct identification of this phenomenon in aging multicellular organisms has not been performed. Here, we express LifeAct::mRuby in a tissue-specific manner to interrogate cytoskeletal organization as a function of age. We show for the first time in Caenorhabditis elegans that the organization and morphology of the actin cytoskeleton deteriorate at advanced age in the muscles, intestine, and hypodermis. Moreover, hsf-1 is essential for regulating cytoskeletal integrity during aging, so that knockdown of hsf-1 results in premature aging of actin and its overexpression protects actin cytoskeletal integrity in the muscles, the intestine, and the hypodermis. Finally, hsf-1 overexpression in neurons alone is sufficient to protect cytoskeletal integrity in nonneuronal cells.

Indexed as

Actin CytoskeletonActinsAgingAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsHomeostasisLongevityNeuronsOrgan SpecificityTranscription FactorsActinsCaenorhabditis elegans Proteinsheat shock factor-1, C elegansTranscription Factors

Identifiers

PMID30133343
PMCPMC6254583
OpenAlexW2888681677

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.