Evidence map›Paper›PMID 25536397›Full record

ArticlePloS one2014

Lipo-chitin oligosaccharides, plant symbiosis signalling molecules that modulate mammalian angiogenesis in vitro.

Michael A Djordjevic, Anna Bezos, Susanti, Laurence Marmuse, Hugues Driguez, Eric Samain, Boris Vauzeilles, Jean-Marie Beau, Farzaneh Kordbacheh, Barry G Rolfe and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.1field-weighted citation impact, top 46% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

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  7. LysMD3 is a type II membrane protein without anThe Journal of biological chemistry · 2018
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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 6 institutions in 3 countries.

Michael A DjordjevicResearch School of Biology, Plant Science Division, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
Anna BezosJohn Curtin School of Medical Research, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
SusantiJohn Curtin School of Medical Research, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
Laurence MarmuseUniversity Grenoble Alpes, CERMAV, Grenoble, France CNRS, CERMAV, Grenoble, France.
Hugues DriguezUniversity Grenoble Alpes, CERMAV, Grenoble, France CNRS, CERMAV, Grenoble, France.
Eric SamainUniversity Grenoble Alpes, CERMAV, Grenoble, France CNRS, CERMAV, Grenoble, France.
Boris VauzeillesUniversity Paris Sud, Institut de Chimie Moléculaire et des Matériaux d'Orsay, Orsay, France, and Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles du CNRS, Gif-sur-Yvette, France.
Jean-Marie BeauUniversity Paris Sud, Institut de Chimie Moléculaire et des Matériaux d'Orsay, Orsay, France, and Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles du CNRS, Gif-sur-Yvette, France.
Farzaneh KordbachehResearch School of Biology, Plant Science Division, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
Barry G RolfeResearch School of Biology, Plant Science Division, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
Ralf SchwörerFerrier Research Institute, Victoria University of Wellington, Lower Hutt Wellington, New Zealand.
Alison M DainesFerrier Research Institute, Victoria University of Wellington, Lower Hutt Wellington, New Zealand.
Peter M GresshoffThe Centre for Integrative Legume Research, The University of Queensland, St Lucia, Brisbane, Queensland, Australia.
Christopher R ParishJohn Curtin School of Medical Research, College of Medicine, Biology and the Environment, Australian National University, Canberra, ACT, Australia.
Australian National University · AUUniversité Grenoble Alpes · FRVictoria University of Wellington · NZCentre National de la Recherche Scientifique · FRInstitut de Chimie Moléculaire et des Matériaux d'Orsay · FRUniversity of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lipochitin oligosaccharides (LCOs) are signaling molecules required by ecologically and agronomically important bacteria and fungi to establish symbioses with diverse land plants. In plants, oligo-chitins and LCOs can differentially interact with different lysin motif (LysM) receptors and affect innate immunity responses or symbiosis-related pathways. In animals, oligo-chitins also induce innate immunity and other physiological responses but LCO recognition has not been demonstrated. Here LCO and LCO-like compounds are shown to be biologically active in mammals in a structure dependent way through the modulation of angiogenesis, a tightly-regulated process involving the induction and growth of new blood vessels from existing vessels. The testing of 24 LCO, LCO-like or oligo-chitin compounds resulted in structure-dependent effects on angiogenesis in vitro leading to promotion, or inhibition or nil effects. Like plants, the mammalian LCO biological activity depended upon the presence and type of terminal substitutions. Un-substituted oligo-chitins of similar chain lengths were unable to modulate angiogenesis indicating that mammalian cells, like plant cells, can distinguish between LCOs and un-substituted oligo-chitins. The cellular mode-of-action of the biologically active LCOs in mammals was determined. The stimulation or inhibition of endothelial cell adhesion to vitronectin or fibronectin correlated with their pro- or anti-angiogenic activity. Importantly, novel and more easily synthesised LCO-like disaccharide molecules were also biologically active and de-acetylated chitobiose was shown to be the primary structural basis of recognition. Given this, simpler chitin disaccharides derivatives based on the structure of biologically active LCOs were synthesised and purified and these showed biological activity in mammalian cells. Since important chronic disease states are linked to either insufficient or excessive angiogenesis, LCO and LCO-like molecules may have the potential to be a new, carbohydrate-based class of therapeutics for modulating angiogenesis.

Indexed as

AcetylationAcylationAnimalsAortaCell AdhesionCell MovementDisaccharidesEndothelial CellsExtracellular MatrixGlycine maxHumansIntegrinsIn Vitro TechniquesLipopolysaccharidesMammalsNeovascularization, PhysiologicchitobioseDisaccharidesIntegrinslipid-linked oligosaccharidesLipopolysaccharides

Identifiers

PMID25536397
PMCPMC4275186
OpenAlexW2041904087

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.