Evidence map›Paper›PMID 36556434›Full record

ArticleLife (Basel, Switzerland)2022

Computational Model Exploring Characteristic Pattern Regulation in Periventricular Vessels.

Hisako Takigawa-Imamura, Saito Hirano, Chisato Watanabe, Chiaki Ohtaka-Maruyama, Masatsugu Ema, Ken-Ichi Mizutani

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Hisako Takigawa-ImamuraAnatomy and Cell Biology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.ORCID 0000-0001-6355-1254
Saito HiranoYahata Kousei Hospital, 3-12-12 Satonaka, Yahatanishi-ku, Kitakyushu 807-0846, Japan.
Chisato WatanabeDepartment of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Otsu 520-2192, Japan.
Chiaki Ohtaka-MaruyamaDevelopmental Neuroscience Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 156-8506, Japan.
Masatsugu EmaDepartment of Stem Cells and Human Disease Models, Research Center for Animal Life Science, Shiga University of Medical Science, Otsu 520-2192, Japan.ORCID 0000-0003-0645-6183
Ken-Ichi MizutaniLaboratory of Stem Cell Biology, Graduate School of Pharmaceutical Sciences, Kobe Gakuin University, 1-1-3 Minatojima, Chuo-ku, Kobe 650-8586, Japan.

Funding

Ministry of Education, Culture, Sports, Science and Technology/Japan Society for the Promotion of Science 19K07259Ministry of Education, Culture, Sports, Science and Technology/Japan Society for the Promotion of Science 22K06802Ministry of Education, Culture, Sports, Science and Technology/Japan Society for the Promotion of Science, Grants-in-Aid 17K07428Ministry of Education, Culture, Sports, Science and Technology/Japan Society for the Promotion of Science, Grants-in-Aid 18K06260Ministry of Education, Culture, Sports, Science and Technology/Japan Society for the Promotion of Science, Grants-in-Aid 19H04795Naito Foundation Y2018Takeda Science Foundation Y2018
6 · The paper itself

Abstract

The developing neocortical vasculature exhibits a distinctive pattern in each layer. In murine embryos, vessels in the cortical plate (CP) are vertically oriented, whereas those in the intermediate zone (IZ) and the subventricular zone (SVZ) form a honeycomb structure. The formation of tissue-specific vessels suggests that the behavior of endothelial cells is under a specific regulatory regime in each layer, although the mechanisms involved remain unknown. In the present study, we aimed to explore the conditions required to form these vessel patterns by conducting simulations using a computational model. We developed a novel model framework describing the collective migration of endothelial cells to represent the angiogenic process and performed a simulation using two-dimensional approximation. The attractive and repulsive guidance of tip cells was incorporated into the model based on the function and distribution of guidance molecules such as VEGF and Unc ligands. It is shown that an appropriate combination of guidance effects reproduces both the parallel straight pattern in the CP and meshwork patterns in the IZ/SVZ. Our model demonstrated how the guidance of the tip cell causes a variety of vessel patterns and predicted how tissue-specific vascular formation was regulated in the early development of neocortical vessels.

Indexed as

angiogenesisendothelial cellmathematical modelneocortical vasculaturepattern formation

Identifiers

PMID36556434
PMCPMC9788473

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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.