Evidence map›Paper›PMID 40503790›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2026

Differential sensitivity of midline development to mitosis during and after primitive streak extension.

Zhiling Zhao, Rieko Asai, Takashi Mikawa

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Zhiling ZhaoCardiovascular Research Institute, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0003-0623-5057
Rieko AsaiCardiovascular Research Institute, University of California San Francisco, San Francisco, California, USA.
Takashi MikawaCardiovascular Research Institute, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0003-1051-8260

Funding

PREDOCTORAL TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007470 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Todd Nystul · 1994 to 2026
$7.7M
Induction and Patterning of Cardiogenic FieldsR01HL153736 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIKAWA, TAKASHI · 2020 to 2023
$1.6M
Development of Vascular Smooth Muscle Stem Cell NicheR01HL148125 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MIKAWA, TAKASHI · 2019 to 2022
$1.6M
Eunice Kennedy Shriver National Institute of Child Health and Human Development T32HD007470JSPS Postdoctoral Fellowship for Research AbroadNHLBI NIH HHS R01 HL148125NHLBI NIH HHS R01 HL153736NICHD NIH HHS T32 HD007470Uehara Memorial Foundation Fellowship
6 · The paper itself

Abstract

backgroundMidline establishment is a fundamental process during early embryogenesis for Bilaterians. Midline morphogenesis in non-amniotes can occur without mitosis, through Planar Cell Polarity (PCP) signaling. By contrast, amniotes utilize both cellular processes for developing the early midline landmark, the primitive streak (PS). This study focused on the role of cell proliferation for midline development at pre- and post-PS-extension stages and analyzed PCP signaling components at post-PS-extension stages.

resultsIn contrast to pre-PS-extension stages, embryos under mitotic arrest during the post-PS-extension preserved notochord (NC) extension and Hensen's node (HN)/PS regression judged by both morphology and marker genes; although they became shorter, their lengths remained proportional to the embryo length. Laterality and segmentation of paraxial mesoderm were lost upon mitotic arrest. Accompanied by mitotic arrest-induced embryonic size reduction, cells including midline tissue displayed hypertrophy.

conclusionThis study has identified at least two distinct mitosis sensitivity phases during early midline development: One is PS extension that requires both mitosis and PCP, and the other is mitotic arrest-resistant midline development at post-PS-extension stages, with a still undefined influence by PCP signaling components.

Indexed as

MitosisPrimitive StreakAnimalsCell PolarityEmbryonic DevelopmentEmbryo, NonmammalianNotochordSignal Transductioncell hypertrophycell proliferationembryo sizemidline patterningnotochordPCPprimitive streak

Identifiers

PMID40503790
PMCPMC12354007

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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.