Evidence map›Paper›PMID 10856127›Full record

ArticleThe Journal of physiology2000

Regulation of the endothelin system by shear stress in human endothelial cells.

H Morawietz, R Talanow, M Szibor, U Rueckschloss, A Schubert, B Bartling, D Darmer, J Holtz

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 166 citations in OpenAlex.

  1. Review
  2. Macrophage Polarization Profiling in Dynamic Culture System.Cellular and molecular bioengineering · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Integrating molecular and cellular components of endothelial shear stress mechanotransduction.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. New insights into mechanisms of endothelial insulin resistance in type 2 diabetes.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Rebuttal from Volker Adams.The Journal of physiology · 2018
    Article
  20. Prolonged sitting leg vasculopathy: contributing factors and clinical implications.American journal of physiology. Heart and circulatory physiology · 2017
    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

8 authors at 2 institutions in 1 country.

H MorawietzInstitute of Pathophysiology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, D-06097 Halle, Germany. henning.morawietz@medizin.uni-halle.de
R Talanow
M Szibor
U Rueckschloss
A Schubert
B Bartling
D Darmer
J Holtz
Martin Luther University Halle-Wittenberg · DELeipzig Heart Institute · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, the effect of shear stress on the expression of genes of the human endothelin-1 system was examined. Primary cultures of human umbilical vein endothelial cells (HUVEC) were exposed to laminar shear stress of 1, 15 or 30 dyn cm-2 (i.e. 0.1, 1.5 or 3 N m-2) (venous and two different arterial levels of shear stress) in a cone-and-plate viscometer. Laminar shear stress transiently upregulates preproendothelin-1 (ppET-1) mRNA, reaching its maximum after 30 min (approx 1.7-fold increase). In contrast, long-term application of shear stress (24 h) causes downregulation of ppET-1 mRNA in a dose-dependent manner. Arterial levels of shear stress result in downregulation of endothelin-converting enzyme-1 isoform ECE-1a (predominating in HUVEC) to 36.2 +/- 8.5 %, and isoform ECE-1b mRNA to 72.3 +/- 1.9 % of static control level. The endothelin-1 (ET-1) release is downregulated by laminar shear stress in a dose-dependent manner. This downregulation of ppET-1 mRNA and ET-1 release is not affected by inhibition of protein kinase C (PKC), or tyrosine kinase. Inhibition of endothelial NO synthase (L-NAME, 500 microm) prevents downregulation of ppET-1 mRNA by shear stress. In contrast, increasing degrees of long-term shear stress upregulate endothelin receptor type B (ETB) mRNA by a NO- and PKC-, but not tyrosine kinase-dependent mechanism. In conclusion, our data suggest the downregulation of human endothelin synthesis, and an upregulation of the ETB receptor by long-term arterial laminar shear stress. These effects might contribute to the vasoprotective and anti-arteriosclerotic potential of arterial laminar shear stress.

Indexed as

Aspartic Acid EndopeptidasesBlotting, NorthernCells, CulturedEndothelin-1Endothelin-Converting EnzymesEndothelinsEndothelium, VascularEnzyme InhibitorsGene Expression Regulation, EnzymologicHumansMetalloendopeptidasesNG-Nitroarginine Methyl EsterNitric Oxide SynthaseNitric Oxide Synthase Type IIINitroarginineProtein Kinase CAspartic Acid EndopeptidasesECE1 protein, humanEndothelin-1Endothelin-Converting EnzymesEndothelinsEnzyme InhibitorsMetalloendopeptidasesNG-Nitroarginine Methyl EsterNitric Oxide SynthaseNitric Oxide Synthase Type IIINitroarginineNOS3 protein, humanProtein Kinase CProtein PrecursorsRNA, Messenger

Identifiers

PMID10856127
PMCPMC2269966
OpenAlexW2167569025

What OpenQuestion holds

Textmetadata
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.