Evidence map›Paper›PMID 35593401›Full record

ArticleDevelopment (Cambridge, England)2022

A unique form of collective epithelial migration is crucial for tissue fusion in the secondary palate and can overcome loss of epithelial apoptosis.

Teng Teng, Camilla S Teng, Vesa Kaartinen, Jeffrey O Bush

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Orthogonal disentanglement of single-cell multi-omics reveals private and shared drivers of tissue development and pathogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Canonical Wnt signaling is not required forFrontiers in physiology · 2023
    Article
  14. Review
  15. Cleft lip∕palate. From embryology to developmental pathogenesis.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

4 authors at 2 institutions in 1 country.

Teng TengDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.
Camilla S TengDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.
Vesa KaartinenDepartment of Biologic and Materials Sciences, University of Michigan School of Dentistry, Ann Arbor, MI 48109, USA.ORCID 0000-0002-9432-510X
Jeffrey O BushDepartment of Cell and Tissue Biology, University of California San Francisco, San Francisco, CA 94143, USA.ORCID 0000-0002-6053-8756
University of California, San Francisco · USUniversity of Michigan · US

Funding

Signaling control and cellular basis of craniofacial morphogenesis and congenital diseaseR35DE031926 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jeffrey Ohmann Bush · 2022 to 2026
$5.2M
Mechanisms of Eph/Ephrin signaling in craniofacial morphogenesis and craniofrontonasal syndromeR01DE023337 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BUSH, JEFFREY OHMANN · 2013 to 2021
$4.3M
Cellular mechanisms of lip and palate fusionR01DE025877 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BUSH, JEFFREY OHMANN · 2016 to 2020
$2.0M
Cellular and molecular regulation of upper lip fusion by p120-cateninF32DE030367 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TENG, CAMILLA SUE · 2020 to 2022
$204k
NIDCR NIH HHS F32 DE030367NIDCR NIH HHS R01 DE023337NIDCR NIH HHS R01 DE025877NIDCR NIH HHS R35 DE031926
6 · The paper itself

Abstract

Tissue fusion frequently requires the removal of an epithelium that intervenes distinct primordia to form one continuous structure. In the mammalian secondary palate, a midline epithelial seam (MES) forms between two palatal shelves and must be removed to allow mesenchymal confluence. Abundant apoptosis and cell extrusion support their importance in MES removal. However, genetically disrupting the intrinsic apoptotic regulators BAX and BAK within the MES results in complete loss of cell death and cell extrusion, but successful removal of the MES. Novel static- and live-imaging approaches reveal that the MES is removed through streaming migration of epithelial trails and islands to reach the oral and nasal epithelial surfaces. Epithelial trail cells that express the basal epithelial marker ΔNp63 begin to express periderm markers, suggesting that migration is concomitant with differentiation. Live imaging reveals anisotropic actomyosin contractility within epithelial trails, and genetic ablation of actomyosin contractility results in dispersion of epithelial collectives and failure of normal MES migration. These findings demonstrate redundancy between cellular mechanisms of morphogenesis, and reveal a crucial and unique form of collective epithelial migration during tissue fusion.

Indexed as

Cleft PalatePalateActomyosinAnimalsApoptosisEpithelial CellsEpitheliumMammalsActomyosinActomyosinApoptosisCell adhesionCell extrusionCleft lipCleft palateCollective cell migrationCraniofacialFusionLive imagingMouseNMIIANon-muscle myosin IIPalateTgfβ

Identifiers

PMID35593401
PMCPMC9188751
OpenAlexW4280527517

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.