Evidence map›Paper›PMID 36111549›Full record

ArticleBiology open2022

RGS5: a novel role as a hypoxia-responsive protein that suppresses chemokinetic and chemotactic migration in brain pericytes.

Andreas Enström, Robert Carlsson, Ilknur Özen, Gesine Paul

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Global profiling of N-terminal cysteine-dependent degradation mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  6. Review
  7. Biglycan stimulates retinal pathological angiogenesis via up-regulation of CXCL12 expression in pericytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Molecular Regulation of the Response of Brain Pericytes to Hypoxia.International journal of molecular sciences · 2023
    Review
  13. 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

4 authors at 2 institutions in 1 country.

Andreas EnströmTranslational Neurology Group, Department of Clinical Science, Lund University, Lund 221 84, Sweden.ORCID 0000-0001-8792-8028
Robert CarlssonTranslational Neurology Group, Department of Clinical Science, Lund University, Lund 221 84, Sweden.ORCID 0000-0001-5955-2916
Ilknur ÖzenTranslational Neurology Group, Department of Clinical Science, Lund University, Lund 221 84, Sweden.ORCID 0000-0002-5858-864X
Gesine PaulTranslational Neurology Group, Department of Clinical Science, Lund University, Lund 221 84, Sweden.ORCID 0000-0002-6806-2254
Lund University · SEScania (Sweden) · SE

Funding

Cancerfonden 19 0155 Pj 01 HHjärnfonden FO 2020-0106Hjrnfonden FO 2020-0106Lunds UniversitetVetenskapsrådet 2019-01029
6 · The paper itself

Abstract

Adaptive biological mechanisms to hypoxia are crucial to maintain oxygen homeostasis, especially in the brain. Pericytes, cells uniquely positioned at the blood-brain interface, respond fast to hypoxia by expressing regulator of G-protein signalling 5 (RGS5), a negative regulator of G-protein-coupled receptors. RGS5 expression in pericytes is observed in pathological hypoxic environments (e.g. tumours and ischaemic stroke) and associated with perivascular depletion of pericytes and vessel leakage. However, the regulation of RGS5 expression and its functional role in pericytes are not known. We demonstrate that RGS5 acts as a hypoxia-responsive protein in human brain pericytes that is regulated independent of hypoxia inducible factor-1α (HIF-1α), rapidly stabilized under hypoxia, but degraded under normoxic conditions. We show that RGS5 expression desensitizes pericytes to signalling of platelet-derived growth factor-BB (PDGFBB) and sphingosine 1-phosphate (S1P), and blocks chemokinesis or chemotaxis induced by these factors. Our data imply a role for RGS5 in antagonizing pericyte recruitment and retention to blood vessels during hypoxia and support RGS5 as a target in counteracting vessel leakage under pathological hypoxic conditions. This article has an associated First Person interview with the first author of the paper.

Indexed as

Brain IschemiaPericytesRGS ProteinsStrokeBrainGTP-Binding ProteinsHumansHypoxiaOxygenPlatelet-Derived Growth FactorReceptors, G-Protein-CoupledGTP-Binding ProteinsOxygenPlatelet-Derived Growth FactorReceptors, G-Protein-CoupledRGS5 protein, humanRGS ProteinsHypoxiaMigrationPDGFBBPericytesRGS5S1P

Identifiers

PMID36111549
PMCPMC9596146
OpenAlexW4296034619

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.