Evidence map›Paper›PMID 33127887›Full record

ArticleNature communications2020

Marcksl1 modulates endothelial cell mechanoresponse to haemodynamic forces to control blood vessel shape and size.

Igor Kondrychyn, Douglas J Kelly, Núria Taberner Carretero, Akane Nomori, Kagayaki Kato, Jeronica Chong, Hiroyuki Nakajima, Satoru Okuda, Naoki Mochizuki, Li-Kun Phng

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.3field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Igor KondrychynLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.ORCID 0000-0002-2268-7291
Douglas J KellyLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Núria Taberner CarreteroLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.ORCID 0000-0002-9234-5473
Akane NomoriLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Kagayaki KatoBioimage Informatics Group, Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, Okazaki, Aichi, 444-8585, Japan.ORCID 0000-0003-4757-3773
Jeronica ChongLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan.
Hiroyuki NakajimaDepartment of Cell Biology and AMED-CREST, National Cerebral and Cardiovascular Center, Research Institute, Suita, Osaka, 565-8565, Japan.ORCID 0000-0003-4139-2779
Satoru OkudaWPI Nano Life Science Institute, Kanazawa University, Kanazawa, 920-1192, Japan.ORCID 0000-0003-3792-8067
Naoki MochizukiDepartment of Cell Biology and AMED-CREST, National Cerebral and Cardiovascular Center, Research Institute, Suita, Osaka, 565-8565, Japan.ORCID 0000-0002-3938-9602
Li-Kun PhngLaboratory for Vascular Morphogenesis, RIKEN Center for Biosystems Dynamics Research, Kobe, 650-0047, Japan. likun.phng@riken.jp.ORCID 0000-0001-8523-9958
RIKEN Center for Biosystems Dynamics Research · JPNational Cerebral and Cardiovascular Center · JPKanazawa University · JPNational Institute for Basic Biology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation of vascular tubes is driven by extensive changes in endothelial cell (EC) shape. Here, we have identified a role of the actin-binding protein, Marcksl1, in modulating the mechanical properties of EC cortex to regulate cell shape and vessel structure during angiogenesis. Increasing and depleting Marcksl1 expression level in vivo results in an increase and decrease, respectively, in EC size and the diameter of microvessels. Furthermore, endothelial overexpression of Marcksl1 induces ectopic blebbing on both apical and basal membranes, during and after lumen formation, that is suppressed by reduced blood flow. High resolution imaging reveals that Marcksl1 promotes the formation of linear actin bundles and decreases actin density at the EC cortex. Our findings demonstrate that a balanced network of linear and branched actin at the EC cortex is essential in conferring cortical integrity to resist the deforming forces of blood flow to regulate vessel structure.

Indexed as

ActinsActomyosinAnimalsAnimals, Genetically ModifiedBlood VesselsCalmodulin-Binding ProteinsEndothelial CellsGene Expression Regulation, DevelopmentalHemodynamicsMicrofilament ProteinsModels, AnimalTranscriptomeZebrafishActinsActomyosinCalmodulin-Binding ProteinsMicrofilament Proteins

Identifiers

PMID33127887
PMCPMC7603353
OpenAlexW3096319071

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.