Evidence map›Paper›PMID 37354904›Full record

ArticleImmunity2023

Lipids regulate peripheral serotonin release via gut CD1d.

Jialie Luo, Zuojia Chen, David Castellano, Bin Bao, Wenyan Han, Jian Li, Girak Kim, Dingding An, Wei Lu, Chuan Wu

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

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  5. Current research in microbial sciences · 2026
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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

10 authors at 3 institutions in 1 country.

Jialie LuoExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA.
Zuojia ChenExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA.
David CastellanoSynapse and Neural Circuit Research Section, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD, USA.
Bin BaoDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Wenyan HanSynapse and Neural Circuit Research Section, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD, USA.
Jian LiExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA.
Girak KimExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA.
Dingding AnDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Wei LuSynapse and Neural Circuit Research Section, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD, USA.
Chuan WuExperimental Immunology Branch, National Cancer Institute, NIH, Bethesda, MD, USA. Electronic address: chuan.wu@nih.gov.
National Cancer Institute · USNational Institute of Neurological Disorders and Stroke · USBoston Children's Hospital · US

Funding

The regulation of synaptic transmission and neural circuit functionZIANS003136 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI LU, WEI · 2012 to 2025
$27.0M
T cell regulation for intestinal barrier functionZIABC011801 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WU, CHUAN · 2018 to 2025
$4.1M
Immune-neuron crosstalk regulates intestinal homeostasisZIABC012034 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WU, CHUAN · 2021 to 2025
$2.0M
Intramural NIH HHS ZIA BC012034
6 · The paper itself

Abstract

The crosstalk between the immune and neuroendocrine systems is critical for intestinal homeostasis and gut-brain communications. However, it remains unclear how immune cells participate in gut sensation of hormones and neurotransmitters release in response to environmental cues, such as self-lipids and microbial lipids. We show here that lipid-mediated engagement of invariant natural killer T (iNKT) cells with enterochromaffin (EC) cells, a subset of intestinal epithelial cells, promoted peripheral serotonin (5-HT) release via a CD1d-dependent manner, regulating gut motility and hemostasis. We also demonstrated that inhibitory sphingolipids from symbiotic microbe Bacteroides fragilis represses 5-HT release. Mechanistically, CD1d ligation on EC cells transduced a signal and restrained potassium conductance through activation of protein tyrosine kinase Pyk2, leading to calcium influx and 5-HT secretion. Together, our data reveal that by engaging with iNKT cells, gut chemosensory cells selectively perceive lipid antigens via CD1d to control 5-HT release, modulating intestinal and systemic homeostasis.

Indexed as

Natural Killer T-CellsSerotoninAntigens, CD1dLipidsAntigens, CD1dLipidsSerotoninCD1denterochromaffin cellsiNKT cellsKv1.2Pyk2serotonin

Identifiers

PMID37354904
PMCPMC10527042
OpenAlexW4381851526

What OpenQuestion holds

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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.