Evidence map›Paper›PMID 32316253›Full record

ArticleCells2020

The Lipopeptide MALP-2 Promotes Collateral Growth.

Kerstin Troidl, Christian Schubert, Ann-Kathrin Vlacil, Ramesh Chennupati, Sören Koch, Jutta Schütt, Raghav Oberoi, Wolfgang Schaper, Thomas Schmitz-Rixen, Bernhard Schieffer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 15 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

11 authors at 3 institutions in 1 country.

Kerstin TroidlMax-Planck-Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.ORCID 0000-0002-0883-9949
Christian SchubertDepartment of Vascular and Endovascular Surgery, University Hospital Frankfurt, 60488 Frankfurt, Germany.
Ann-Kathrin VlacilCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Ramesh ChennupatiMax-Planck-Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.
Sören KochCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Jutta SchüttCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Raghav OberoiCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Wolfgang SchaperMax-Planck-Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.
Thomas Schmitz-RixenDepartment of Vascular and Endovascular Surgery, University Hospital Frankfurt, 60488 Frankfurt, Germany.ORCID 0000-0002-6082-0006
Bernhard SchiefferCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Karsten GroteCardiology and Angiology, Philipps-University Marburg, 35043 Marburg, Germany.
Philipps University of Marburg · DEGoethe University Frankfurt · DEMax Planck Institute for Heart and Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Beyond their role in pathogen recognition and the initiation of immune defense, Toll-like receptors (TLRs) are known to be involved in various vascular processes in health and disease. We investigated the potential of the lipopeptide and TLR2/6 ligand macrophage activating protein of 2-kDA (MALP-2) to promote blood flow recovery in mice. Hypercholesterolemic apolipoprotein E (Apoe)-deficient mice were subjected to microsurgical ligation of the femoral artery. MALP-2 significantly improved blood flow recovery at early time points (three and seven days), as assessed by repeated laser speckle imaging, and increased the growth of pre-existing collateral arteries in the upper hind limb, along with intimal endothelial cell proliferation in the collateral wall and pericollateral macrophage accumulation. In addition, MALP-2 increased capillary density in the lower hind limb. MALP-2 enhanced endothelial nitric oxide synthase (eNOS) phosphorylation and nitric oxide (NO) release from endothelial cells and improved the experimental vasorelaxation of mesenteric arteries ex vivo. In vitro, MALP-2 led to the up-regulated expression of major endothelial adhesion molecules as well as their leukocyte integrin receptors and consequently enhanced the endothelial adhesion of leukocytes. Using the experimental approach of femoral artery ligation (FAL), we achieved promising results with MALP-2 to promote peripheral blood flow recovery by collateral artery growth.

Indexed as

AnimalsApolipoproteins EBlood CirculationCapillariesCell ProliferationEndothelial CellsFemoral ArteryImmunohistochemistryLaser Speckle Contrast ImagingLipopeptidesMacrophagesMaleMiceMice, Inbred BALB CMice, Inbred C57BLMonocytesApolipoproteins ELipopeptidesmacrophage stimulatory lipopeptide 2Nitric OxideNitric Oxide SynthaseTlr2 protein, mouseTlr6 protein, mouseToll-Like Receptor 2Toll-Like Receptor 6blood flow recoverycollateral growthfemoral artery ligationTLR2/6

Identifiers

PMID32316253
PMCPMC7227808
OpenAlexW3017153762

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.