Evidence map›Paper›PMID 31957193›Full record

ArticleCell proliferation2020

Human monocytes subjected to ischaemia/reperfusion inhibit angiogenesis and wound healing in vitro.

Lars Hummitzsch, Martin Albrecht, Karina Zitta, Katharina Hess, Kerstin Parczany, René Rusch, Jochen Cremer, Markus Steinfath, Assad Haneya, Fred Faendrich and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 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
0.7field-weighted citation impact, top 32% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Monocyte recruitment and fate specification after myocardial infarction.American journal of physiology. Cell physiology · 2020
    Review
  8. Article
  9. Article
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 2 institutions in 1 country.

Lars HummitzschDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Kiel, Germany.
Martin AlbrechtDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Kiel, Germany.ORCID https://orcid.org/0000-0003-2580-768X
Karina ZittaDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Kiel, Germany.
Katharina HessInstitute of Neuropathology, University Hospital Muenster, Muenster, Germany.
Kerstin ParczanyDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Kiel, Germany.
René RuschDepartment of Cardiovascular Surgery, University Hospital of Schleswig-Holstein, Kiel, Germany.
Jochen CremerDepartment of Cardiovascular Surgery, University Hospital of Schleswig-Holstein, Kiel, Germany.
Markus SteinfathDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Schleswig-Holstein, Kiel, Germany.
Assad HaneyaDepartment of Cardiovascular Surgery, University Hospital of Schleswig-Holstein, Kiel, Germany.
Fred FaendrichDepartment of Applied Cell Therapy, University Hospital of Schleswig-Holstein, Kiel, Germany.
Rouven BerndtDepartment of Cardiovascular Surgery, University Hospital of Schleswig-Holstein, Kiel, Germany.ORCID https://orcid.org/0000-0002-4053-6235
University Hospital Schleswig-Holstein · DEUniversity Hospital Münster · DE

Funding

Schleswig-Holstein's Ministry of Science, Economy and Transport F359921
6 · The paper itself

Abstract

objectivesThe sequence of initial tissue ischaemia and consecutive blood flow restoration leads to ischaemia/reperfusion (I/R) injury, which is typically characterized by a specific inflammatory response. Migrating monocytes seem to mediate the immune response in ischaemic tissues and influence detrimental as well as regenerative effects during I/R injury. MATERIALS AND

methodsTo clarify the role of classical monocytes in I/R injury, isolated human monocytes were subjected to I/R in vitro (3 hours ischaemia followed by 24 hours of reperfusion). Cellular resilience, monocyte differentiation, cytokine secretion, as well as influence on endothelial tube formation, migration and cell recovery were investigated.

resultsWe show that I/R supported an enhanced resilience of monocytes and induced intracellular phosphorylation of the prosurvival molecules Erk1/2 and Akt. FACS analysis showed no major alteration in monocyte subtype differentiation and surface marker expression under I/R. Further, our experiments revealed that I/R changes the cytokine secretion pattern, release of angiogenesis associated proteins and MMP-9 activity in supernatants of monocytes exposed to I/R. Supernatants from monocytes subjected to I/R attenuated endothelial tube formation as indicator for angiogenesis as well as endothelial cell migration and recovery.

conclusionIn summary, monocytes showed no significant change in cellular integrity and monocyte subtype after I/R. Functionally, monocytes might have a rather detrimental influence during the initial phase of I/R, suppressing endothelial cell migration and neoangiogenesis.

Indexed as

Cell DifferentiationCell MovementCells, CulturedCytokinesEndothelial CellsHumansMonocytesNeovascularization, PathologicReperfusion InjuryWound HealingCytokinescytokinesischaemia/reperfusion injurymonocytesneoangiogenesisremodellingwound healing

Identifiers

PMID31957193
PMCPMC7048205
OpenAlexW3001228980

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.