Evidence map›Paper›PMID 30260505›Full record

ArticleGlia2018

Glio- and neuro-protection by prosaposin is mediated by orphan G-protein coupled receptors GPR37L1 and GPR37.

Beihui Liu, Valentina Mosienko, Barbara Vaccari Cardoso, Daria Prokudina, Mathew Huentelman, Anja G Teschemacher, Sergey Kasparov

Open access · hybridAbstract read
In one paragraph

Article in Glia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

63 citing papers in PubMed, 94 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Prosaposin in CNS health and disease, metabolic stress and exercise adaptation.Journal of molecular medicine (Berlin, Germany) · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. GNature communications · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Loss of Inpp5d has disease-relevant and sex-specific effects on glial transcriptomes.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  19. Gz Enhanced Signal Transduction assaY (GbioRxiv : the preprint server for biology · 2024
    Article
  20. Review

3 more citing papers are in PubMed but not listed here.

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

7 authors at 3 institutions in 3 countries.

Beihui LiuDepartment of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, United Kingdom.
Valentina MosienkoDepartment of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, United Kingdom.
Barbara Vaccari CardosoDepartment of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, United Kingdom.
Daria ProkudinaBaltic Federal University, Kaliningrad, Russia Federation.
Mathew HuentelmanTranslational Genomics Research Institute (TGen), Phoenix, Arizona.
Anja G TeschemacherDepartment of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, United Kingdom.
Sergey KasparovDepartment of Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-1824-1764
University of Bristol · GBImmanuel Kant Baltic Federal University · RUTranslational Genomics Research Institute · US

Funding

Biotechnology and Biological Sciences Research Council BB/L019396/1Medical Research Council MR/L020661/1
6 · The paper itself

Abstract

Discovery of neuroprotective pathways is one of the major priorities for neuroscience. Astrocytes are natural neuroprotectors and it is likely that brain resilience can be enhanced by mobilizing their protective potential. Among G-protein coupled receptors expressed by astrocytes, two highly related receptors, GPR37L1 and GPR37, are of particular interest. Previous studies suggested that these receptors are activated by a peptide Saposin C and its neuroactive fragments (prosaptide TX14(A)), which were demonstrated to be neuroprotective in various animal models by several groups. However, pairing of Saposin C or prosaptides with GPR37L1/GPR37 has been challenged and presently GPR37L1/GPR37 have regained their orphan status. Here, we demonstrate that in their natural habitat, astrocytes, these receptors mediate a range of effects of TX14(A), including protection from oxidative stress. The Saposin C/GPR37L1/GPR37 pathway is also involved in the neuroprotective effect of astrocytes on neurons subjected to oxidative stress. The action of TX14(A) is at least partially mediated by Gi-proteins and the cAMP-PKA axis. On the other hand, when recombinant GPR37L1 or GPR37 are expressed in HEK293 cells, they are not functional and do not respond to TX14(A), which explains unsuccessful attempts to confirm the ligand-receptor pairing. Therefore, this study identifies GPR37L1/GPR37 as the receptors for TX14(A), and, by extension of Saposin C, and paves the way for the development of neuroprotective therapeutics acting via these receptors.

Indexed as

Adjuvants, ImmunologicAnimalsAnimals, NewbornAstrocytesCell MovementCells, CulturedCerebral CortexColforsinCyclic AMPEmbryo, MammalianHEK293 CellsHumansL-Lactate DehydrogenaseNerve Growth FactorsNeuronsNeuroprotective AgentsAdjuvants, ImmunologicColforsinCyclic AMPL-Lactate DehydrogenaseNerve Growth FactorsNeuroprotective AgentsprosaptidePsap protein, ratReceptors, G-Protein-CoupledSaposinsWaterastrocyteastroprotectioncAMPGPR37GPR37L1neuroprotectionorphan receptorsPKAprosaptideSaposin C

Identifiers

PMID30260505
PMCPMC6492175
OpenAlexW2894074987

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.