Evidence map›Paper›PMID 37039481›Full record

ArticleeLife2023

Transmembrane protein CD69 acts as an S1PR1 agonist.

Hongwen Chen, Yu Qin, Marissa Chou, Jason G Cyster, Xiaochun Li

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. 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
4.6field-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

26 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. CD8MedComm · 2026
    Review
  3. Review
  4. bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Article
  7. CD8Nature reviews. Cardiology · 2026
    Review
  8. Review
  9. Article
  10. The spleen-brain axis in Alzheimer's disease and related dementias: Integrating immune and metabolic regulation.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  11. Article
  12. A viral glycoprotein targets IgGEMBO molecular medicine · 2026
    Article
  13. Resident CD49aScience advances · 2026
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. CD69Cell communication and signaling : CCS · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Hongwen ChenDepartment of Molecular Genetics, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-1065-9808
Yu QinDepartment of Molecular Genetics, The University of Texas Southwestern Medical Center, Dallas, United States.
Marissa ChouDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, United States.
Jason G CysterDepartment of Microbiology and Immunology, University of California, San Francisco, San Francisco, United States.ORCID 0000-0002-4735-9745
Xiaochun LiDepartment of Molecular Genetics, The University of Texas Southwestern Medical Center, Dallas, United States.ORCID 0000-0002-0177-0803
The University of Texas Southwestern Medical Center · USHoward Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Tissue Culture & Antibody Production CoreP01HL160487 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Helen Haskell Hobbs · 2022 to 2026
$14.9M
Medical Scientist Training Program (T32 NRSA Training Grant)T32GM141323 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Aimee Kao · 2021 to 2026
$10.5M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeff G McDonald · 2022 to 2026
$7.4M
B LYMPHOCYTE MIGRATION AND HOMEOSTASISR01AI040098 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jason G Cyster · 1997 to 2026
$7.0M
Structural and Functional investigations of Hedgehog Signaling TransductionR01GM135343 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI LI, XIAOCHUN · 2019 to 2022
$1.2M
NHLBI NIH HHS P01 HL160487NIAID NIH HHS R01 AI040098NIDDK NIH HHS P30 DK127984NIGMS NIH HHS R01 GM135343NIGMS NIH HHS T32 GM141323
6 · The paper itself

Abstract

The activation of Sphingosine-1-phosphate receptor 1 (S1PR1) by S1P promotes lymphocyte egress from lymphoid organs, a process critical for immune surveillance and T cell effector activity. Multiple drugs that inhibit S1PR1 function are in use clinically for the treatment of autoimmune diseases. Cluster of Differentiation 69 (CD69) is an endogenous negative regulator of lymphocyte egress that interacts with S1PR1 in cis to facilitate internalization and degradation of the receptor. The mechanism by which CD69 causes S1PR1 internalization has been unclear. Moreover, although there are numerous class A GPCR structures determined with different small molecule agonists bound, it remains unknown whether a transmembrane protein per se can act as a class A GPCR agonist. Here, we present the cryo-EM structure of CD69-bound S1PR1 coupled to the heterotrimeric G

Indexed as

LymphocytesReceptors, LysosphingolipidCD69 AntigensImmunologic FactorsMembrane ProteinsT-LymphocytesCD69 AntigensImmunologic FactorsMembrane ProteinsReceptors, LysosphingolipidHEK293humanmolecular biophysicsstructural biologyWEHI231

Identifiers

PMID37039481
PMCPMC10154026
OpenAlexW4364352057

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.