Evidence map›Paper›PMID 32894222›Full record

ArticleeLife2020

Keratins and the plakin family cytolinker proteins control the length of epithelial microridge protrusions.

Yasuko Inaba, Vasudha Chauhan, Aaron Paul van Loon, Lamia Saiyara Choudhury, Alvaro Sagasti

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. 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
2.0field-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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. mTOR signaling governs the formation of epithelial apical projections via S6K1-RhoA and aPKC-Lgl2 axes.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Genomic adaptations for arboreal locomotion in Asian flying treefrogs.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Article
  11. Hemidesmosome-Related Keratin Filament Bundling and Nucleation.International journal of molecular sciences · 2021
    Article
  12. Article
  13. Tools of the trade: studying actin in zebrafish.Histochemistry and cell biology · 2020
    Review
  14. 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

5 authors at 1 institution in 1 country.

Yasuko InabaMolecular, Cell and Developmental Biology Department and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, United States.ORCID 0000-0002-3239-2075
Vasudha ChauhanMolecular, Cell and Developmental Biology Department and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, United States.
Aaron Paul van LoonMolecular, Cell and Developmental Biology Department and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, United States.
Lamia Saiyara ChoudhuryMolecular, Cell and Developmental Biology Department and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, United States.
Alvaro SagastiMolecular, Cell and Developmental Biology Department and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, United States.ORCID 0000-0002-6823-0692
University of California, Los Angeles · US

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
Cytoskeletal Control of Microridge Morphogenesis on Mucosal Epithelial Cells of the Zebrafish SkinR01GM122901 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAGASTI, ALVARO · 2017 to 2021
$1.2M
The morphogenesis of actin-based structures in mucosal epitheliaR21EY024400 · NEI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SAGASTI, ALVARO · 2014 to 2015
$404k
NEI NIH HHS R21 EY024400NIGMS NIH HHS GM007185NIGMS NIH HHS R01 GM122901NIGMS NIH HHS T32 GM007185
6 · The paper itself

Abstract

Actin filaments and microtubules create diverse cellular protrusions, but intermediate filaments, the strongest and most stable cytoskeletal elements, are not known to directly participate in the formation of protrusions. Here we show that keratin intermediate filaments directly regulate the morphogenesis of microridges, elongated protrusions arranged in elaborate maze-like patterns on the surface of mucosal epithelial cells. We found that microridges on zebrafish skin cells contained both actin and keratin filaments. Keratin filaments stabilized microridges, and overexpressing keratins lengthened them. Envoplakin and periplakin, plakin family cytolinkers that bind F-actin and keratins, localized to microridges, and were required for their morphogenesis. Strikingly, plakin protein levels directly dictate microridge length. An actin-binding domain of periplakin was required to initiate microridge morphogenesis, whereas periplakin-keratin binding was required to elongate microridges. These findings separate microridge morphogenesis into distinct steps, expand our understanding of intermediate filament functions, and identify microridges as protrusions that integrate actin and intermediate filaments.

Indexed as

Cell Surface ExtensionsKeratinsPlakinsAnimalsEpithelial CellsIntermediate FilamentsMembrane ProteinsProtein PrecursorsSkinZebrafishZebrafish ProteinsenvoplakinKeratinsMembrane ProteinsPlakinsProtein PrecursorsZebrafish Proteinsactincell biologydevelopmental biologykeratinmicroridgemorphogenesisPlakinprotrusionzebrafish

Identifiers

PMID32894222
PMCPMC7535935
OpenAlexW3084170542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.