Evidence map›Paper›PMID 27995929›Full record

ArticleNature communications2016

The biomechanical properties of an epithelial tissue determine the location of its vasculature.

Martin Kragl, Rajib Schubert, Haiko Karsjens, Silke Otter, Barbara Bartosinska, Kay Jeruschke, Jürgen Weiss, Chunguang Chen, David Alsteens, Oliver Kuss and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 21 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

14 authors at 5 institutions in 2 countries.

Martin KraglInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Rajib SchubertEidgenössische Technische Hochschule Zürich, Department of Biosystems Science and Engineering, CH-4058 Basel, Switzerland.
Haiko KarsjensInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Silke OtterInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Barbara BartosinskaInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Kay JeruschkeGerman Center for Diabetes Research (DZD e.V.), D-85764 München-Neuherberg, Germany.
Jürgen WeissGerman Center for Diabetes Research (DZD e.V.), D-85764 München-Neuherberg, Germany.
Chunguang ChenGerman Center for Diabetes Research (DZD e.V.), D-85764 München-Neuherberg, Germany.
David AlsteensEidgenössische Technische Hochschule Zürich, Department of Biosystems Science and Engineering, CH-4058 Basel, Switzerland.
Oliver KussGerman Center for Diabetes Research (DZD e.V.), D-85764 München-Neuherberg, Germany.
Stephan SpeierGerman Center for Diabetes Research (DZD e.V.), D-85764 München-Neuherberg, Germany.
Daniel EberhardInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Daniel J MüllerEidgenössische Technische Hochschule Zürich, Department of Biosystems Science and Engineering, CH-4058 Basel, Switzerland.
Eckhard LammertInstitute of Metabolic Physiology, Department of Biology, Heinrich Heine University, D-40225 Düsseldorf, Germany.
Heinrich Heine University Düsseldorf · DEGerman Center for Diabetes Research · DEDeutsches Diabetes-Zentrum e.V. · DEETH Zurich · CHBoard of the Swiss Federal Institutes of Technology · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An important question is how growing tissues establish a blood vessel network. Here we study vascular network formation in pancreatic islets, endocrine tissues derived from pancreatic epithelium. We find that depletion of integrin-linked kinase (ILK) in the pancreatic epithelial cells of mice results in glucose intolerance due to a loss of the intra-islet vasculature. In turn, blood vessels accumulate at the islet periphery. Neither alterations in endothelial cell proliferation, apoptosis, morphology, Vegfa expression and VEGF-A secretion nor 'empty sleeves' of vascular basement membrane are found. Instead, biophysical experiments reveal that the biomechanical properties of pancreatic islet cells, such as their actomyosin-mediated cortex tension and adhesive forces to endothelial cells, are significantly changed. These results suggest that a sorting event is driving the segregation of endothelial and epithelial cells and indicate that the epithelial biomechanical properties determine whether the blood vasculature invades or envelops a growing epithelial tissue.

Indexed as

ActomyosinAnimalsBasement MembraneBiomechanical PhenomenaCell AdhesionEndothelial CellsEpithelial CellsEpitheliumFemaleGlucose IntoleranceInsulinInsulin SecretionIslets of LangerhansMaleMiceMice, Inbred C57BLActomyosinInsulinProtein Serine-Threonine KinasesScaffold Protein ILKVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID27995929
PMCPMC5187430
OpenAlexW2560873907

What OpenQuestion holds

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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.