Evidence map›Paper›PMID 38562854›Full record

ArticlebioRxiv : the preprint server for biology2024

Cannabinoid Receptor Signaling is Dependent on Sub-Cellular Location.

Alix Thomas, Braden T Lobingier, Carsten Schultz, Aurélien Laguerre

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

Alix ThomasOregon Health and Science University, Department of Chemical Physiology and Biochemistry, Portland, OR, 97239, USA.
Braden T LobingierOregon Health and Science University, Department of Chemical Physiology and Biochemistry, Portland, OR, 97239, USA.
Carsten SchultzOregon Health and Science University, Department of Chemical Physiology and Biochemistry, Portland, OR, 97239, USA.
Aurélien LaguerreOregon Health and Science University, Department of Chemical Physiology and Biochemistry, Portland, OR, 97239, USA.
Oregon Health & Science University · US

Funding

Endosomes as a multifunctional hub to control GPCR functionR35GM137835 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI Braden Lobingier · 2020 to 2026
$2.5M
Chemical biology tools for studying growth factor receptor internalizationR01GM127631 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI SCHULTZ, CARSTEN · 2018 to 2024
$2.4M
Chemical biology tools for investigating heteromeric complexes of cannabinoid receptorsK99GM141316 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI LAGUERRE, AURELIEN · 2021 to 2022
$103k
NIGMS NIH HHS K99 GM141316NIGMS NIH HHS R01 GM127631NIGMS NIH HHS R35 GM137835
6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are membrane bound signaling molecules that regulate many aspects of human physiology. Recent advances have demonstrated that GPCR signaling can occur both at the cell surface and internal cellular membranes. Our findings suggest that cannabinoid receptor 1 (CB1) signaling is highly dependent on its subcellular location. We find that intracellular CB1 receptors predominantly couple to Gαi while plasma membrane receptors couple to Gαs. Here we show subcellular location of CB1, and its signaling, is contingent on the choice of promoters and receptor tags. Heterologous expression with a strong promoter or N-terminal tag resulted in CB1 predominantly localizing to the plasma membrane and signaling through Gαs. Conversely, CB1 driven by low expressing promoters and lacking N-terminal genetic tags largely localized to internal membranes and signals via Gαi. Lastly, we demonstrate that genetically encodable non-canonical amino acids (ncAA) offer a solution to the problem of non-native N-terminal tags disrupting CB1 signaling. We identified sites in CB1R and CB2R which can be tagged with fluorophores without disrupting CB signaling or trafficking using (

Identifiers

PMID38562854
PMCPMC10983902
OpenAlexW4393118158

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.