Evidence map›Paper›PMID 29754289›Full record

ArticleDiabetologia2018

The novel adipokine WISP1 associates with insulin resistance and impairs insulin action in human myotubes and mouse hepatocytes.

Tina Hörbelt, Christopher Tacke, Mariya Markova, Daniella Herzfeld de Wiza, Frederique Van de Velde, Marlies Bekaert, Yves Van Nieuwenhove, Silke Hornemann, Maria Rödiger, Nicole Seebeck and 12 more

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
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  8. An overview of CCN4 (WISP1) role in human diseases.Journal of translational medicine · 2024
    Review
  9. Review
  10. CCN proteins: opportunities for clinical studies-a personal perspective.Journal of cell communication and signaling · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. New Discovered Adipokines Associated with the Pathogenesis of Obesity and Type 2 Diabetes.Diabetes, metabolic syndrome and obesity : targets and therapy · 2022
    Review
  15. Review
  16. Article
  17. Review
  18. Article
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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

22 authors at 7 institutions in 4 countries.

Tina HörbeltInstitute for Biochemistry and Pathobiochemistry, German Diabetes Center, Düsseldorf, Germany.
Christopher TackeGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Mariya MarkovaGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Daniella Herzfeld de WizaInstitute for Biochemistry and Pathobiochemistry, German Diabetes Center, Düsseldorf, Germany.
Frederique Van de VeldeDepartment of Endocrinology, Ghent University Hospital, Ghent, Belgium.
Marlies BekaertDepartment of Endocrinology, Ghent University Hospital, Ghent, Belgium.
Yves Van NieuwenhoveDepartment of Surgery, Ghent University Hospital, Ghent, Belgium.
Silke HornemannGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Maria RödigerGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Nicole SeebeckGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Elisabeth FriedlDepartment of Clinical Nutrition, German Institute of Human Nutrition Potsdam-Rehbruecke, Arthur-Scheunert-Allee 114-116, 14558, Nuthetal, Germany.
Wenke JonasGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
G Hege ThoresenDepartment of Pharmaceutical Biosciences, School of Pharmacy, University of Oslo, Oslo, Norway.
Oliver KussGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Anke RosenthalClinic for Nutritional Medicine, Berlin, Germany.
Volker LangeCenter for Obesity and Metabolic Surgery, Vivantes Hospital, Berlin, Germany.
Andreas F H PfeifferGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Annette SchürmannGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Bruno LapauwDepartment of Endocrinology, Ghent University Hospital, Ghent, Belgium.
Natalia RudovichGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany.
Olga PivovarovaGerman Center for Diabetes Research (DZD), Muenchen-Neuherberg, Germany. Olga.Pivovarova@dife.de.
D Margriet OuwensInstitute for Biochemistry and Pathobiochemistry, German Diabetes Center, Düsseldorf, Germany.ORCID 0000-0001-6709-2702
Deutsches Diabetes-Zentrum e.V. · DEGhent University Hospital · BEGerman Institute of Human Nutrition · DESpital Linth · CHUniversity of Oslo · NOVivantes Klinikum · DEZimmer Biomet (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisWingless-type (Wnt) inducible signalling pathway protein-1 (WISP1) has been recently identified as a proinflammatory adipokine. We examined whether WISP1 expression and circulating levels are altered in type 2 diabetes and whether WISP1 affects insulin signalling in muscle cells and hepatocytes.

methodsSerum and visceral adipose tissue (VAT) biopsies, for analysis of circulating WISP1 levels by ELISA and WISP1 mRNA expression by real-time quantitative RT-PCR, were collected from normal-weight men (control group, n = 33) and obese men with (n = 46) and without type 2 diabetes (n = 56) undergoing surgery. Following incubation of primary human skeletal muscle cells (hSkMCs) and murine AML12 hepatocytes with WISP1 and insulin, insulin signalling was analysed by western blotting. The effect of WISP1 on insulin-stimulated glycogen synthesis and gluconeogenesis was investigated in hSkMCs and murine hepatocytes, respectively.

resultsCirculating WISP1 levels were higher in obese men (independent of diabetes status) than in normal-weight men (mean [95% CI]: 70.8 [55.2, 86.4] ng/l vs 42.6 [28.5, 56.6] ng/l, respectively; p < 0.05). VAT WISP1 expression was 1.9-fold higher in obese men vs normal-weight men (p < 0.05). Circulating WISP1 levels were positively associated with blood glucose in the OGTT and circulating haem oxygenase-1 and negatively associated with adiponectin levels. In hSkMCs and AML12 hepatocytes, recombinant WISP1 impaired insulin action by inhibiting phosphorylation of insulin receptor, Akt and its substrates glycogen synthase kinase 3β, FOXO1 and p70S6 kinase, and inhibiting insulin-stimulated glycogen synthesis and suppression of gluconeogenic genes. CONCLUSIONS/

interpretationCirculating WISP1 levels and WISP1 expression in VAT are increased in obesity independent of glycaemic status. Furthermore, WISP1 impaired insulin signalling in muscle and liver cells.

Indexed as

AnimalsBlood GlucoseCCN Intercellular Signaling ProteinsEnzyme-Linked Immunosorbent AssayHepatocytesHumansInsulin ResistanceIntra-Abdominal FatMiceMuscle Fibers, SkeletalPhosphorylationProto-Oncogene ProteinsReceptor, InsulinSignal TransductionBlood GlucoseCCN4 protein, humanCCN4 protein, mouseCCN Intercellular Signaling ProteinsProto-Oncogene ProteinsReceptor, InsulinAdipokineAktInsulin actionInsulin resistanceType 2 diabetesVisceral adipose tissueWISP1

Identifiers

PMID29754289
OpenAlexW2800166361

What OpenQuestion holds

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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.