Evidence map›Paper›PMID 31386629›Full record

ArticleAging2019

Glycation of macrophages induces expression of pro-inflammatory cytokines and reduces phagocytic efficiency.

Veronika Bezold, Philip Rosenstock, Jonas Scheffler, Henriette Geyer, Rüdiger Horstkorte, Kaya Bork

Open access · greenAbstract readComparative Study
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  17. Acta pharmaceutica Sinica. B · 2023
    Article
  18. Review
  19. Dicarbonyl Stress in Diabetic Vascular Disease.International journal of molecular sciences · 2022
    Review
  20. Review
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

6 authors at 1 institution in 1 country.

Veronika BezoldInstitute for Physiological Chemistry, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Philip RosenstockInstitute for Physiological Chemistry, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Jonas SchefflerInstitute for Physiological Chemistry, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Henriette GeyerOctapharma Biopharmaceuticals GmbH, Molecular Biochemistry, Berlin, Germany.
Rüdiger HorstkorteInstitute for Physiological Chemistry, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Kaya BorkInstitute for Physiological Chemistry, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Martin Luther University Halle-Wittenberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycation and the accumulation of advanced glycation end products (AGEs) are known to occur during normal aging but also in the progression of several diseases, such as diabetes. Diabetes type II and aging both lead to impaired wound healing. It has been demonstrated that macrophages play an important role in impaired wound healing, however, the underlying causes remain unknown. Elevated blood glucose levels as well as elevated methylglyoxal (MGO) levels in diabetic patients result in glycation and increase of AGEs. We used MGO to investigate the influence of glycation and AGEs on macrophages. We could show that glycation, but not treatment with AGE-modified serum proteins, increased expression of pro-inflammatory cytokines interleukin 1β (IL-1β) and IL-8 but also affected IL-10 and TNF-α expression, resulting in increased inflammation. At the same time, glycation reduced phagocytic efficiency and led to impaired clearance rates of invading microbes and cellular debris. Our data suggest that glycation contributes to changes of macrophage activity and cytokine expression and therefore could support the understanding of disturbed wound healing during aging and diabetes.

Indexed as

AgingCytokinesDiabetes Mellitus, Type 2Glycation End Products, AdvancedGlycosylationHumansInflammationInterleukin-10Interleukin-1betaInterleukin-8Macrophage ActivationMacrophagesPhagocytesPyruvaldehydeReactive Oxygen SpeciesTHP-1 CellsCXCL8 protein, humanCytokinesGlycation End Products, AdvancedIL10 protein, humanIL1B protein, humanInterleukin-10Interleukin-1betaInterleukin-8PyruvaldehydeReactive Oxygen SpeciesTumor Necrosis Factor-alphaadvanced glycation end productsagingglycationinflammationmacrophagesmethylglyoxal

Identifiers

PMID31386629
PMCPMC6682540
OpenAlexW2965884920

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.