Evidence map›Paper›PMID 30256801›Full record

ArticlePLoS biology2018

mDia1/3 generate cortical F-actin meshwork in Sertoli cells that is continuous with contractile F-actin bundles and indispensable for spermatogenesis and male fertility.

Satoko Sakamoto, Dean Thumkeo, Hiroshi Ohta, Zhen Zhang, Shuangru Huang, Pakorn Kanchanawong, Takayoshi Fuu, Sadanori Watanabe, Kentaro Shimada, Yoshitaka Fujihara and 5 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.9field-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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Recapitulating Actin Module Organization in theInternational journal of molecular sciences · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Functional integrity of the contractile actin cortex is safeguarded by multiple Diaphanous-related formins.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

15 authors at 4 institutions in 2 countries.

Satoko SakamotoMedical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Dean ThumkeoMedical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-4513-8455
Hiroshi OhtaDepartment of Anatomy and Cell Biology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Zhen ZhangMechanobiology Institute, National University of Singapore, Singapore.
Shuangru HuangMechanobiology Institute, National University of Singapore, Singapore.
Pakorn KanchanawongMechanobiology Institute, National University of Singapore, Singapore.
Takayoshi FuuMedical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Sadanori WatanabeMedical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kentaro ShimadaResearch Institute for Microbial Disease, Osaka University, Osaka, Japan.
Yoshitaka FujiharaResearch Institute for Microbial Disease, Osaka University, Osaka, Japan.
Shosei YoshidaNational Institute for Basic Biology, Okazaki, Japan.
Masahito IkawaResearch Institute for Microbial Disease, Osaka University, Osaka, Japan.
Naoki WatanabeDepartment of Pharmacology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mitinori SaitouDepartment of Anatomy and Cell Biology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Shuh NarumiyaMedical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kyoto University · JPNational University of Singapore · SGThe University of Osaka · JPNational Institute for Basic Biology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Formin is one of the two major classes of actin binding proteins (ABPs) with nucleation and polymerization activity. However, despite advances in our understanding of its biochemical activity, whether and how formins generate specific architecture of the actin cytoskeleton and function in a physiological context in vivo remain largely obscure. It is also unknown how actin filaments generated by formins interact with other ABPs in the cell. Here, we combine genetic manipulation of formins mammalian diaphanous homolog1 (mDia1) and 3 (mDia3) with superresolution microscopy and single-molecule imaging, and show that the formins mDia1 and mDia3 are dominantly expressed in Sertoli cells of mouse seminiferous tubule and together generate a highly dynamic cortical filamentous actin (F-actin) meshwork that is continuous with the contractile actomyosin bundles. Loss of mDia1/3 impaired these F-actin architectures, induced ectopic noncontractile espin1-containing F-actin bundles, and disrupted Sertoli cell-germ cell interaction, resulting in impaired spermatogenesis. These results together demonstrate the previously unsuspected mDia-dependent regulatory mechanism of cortical F-actin that is indispensable for mammalian sperm development and male fertility.

Indexed as

FertilitySpermatogenesisActinsActomyosinAdherens JunctionsAnimalsCarrier ProteinsCell AdhesionCells, CulturedForminsMaleMice, Inbred C57BLMice, KnockoutPolymerizationSeminiferous TubulesSertoli CellsActinsActomyosinCarrier ProteinsDiap1 protein, mouseDiap2 protein, mouseFormins

Identifiers

PMID30256801
PMCPMC6175529
OpenAlexW2894090449

What OpenQuestion holds

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LicenceCC BY
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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.