» Articles » PMID: 34176785

Single-Cell Mapping of GLP-1 and GIP Receptor Expression in the Dorsal Vagal Complex

Overview
Journal Diabetes
Specialty Endocrinology
Date 2021 Jun 28
PMID 34176785
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The dorsal vagal complex (DVC) in the hindbrain, composed of the area postrema, nucleus of the solitary tract, and dorsal motor nucleus of the vagus, plays a critical role in modulating satiety. The incretins glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) act directly in the brain to modulate feeding, and receptors for both are expressed in the DVC. Given the impressive clinical responses to pharmacologic manipulation of incretin signaling, understanding the central mechanisms by which incretins alter metabolism and energy balance is of critical importance. Here, we review recent single-cell approaches used to detect molecular signatures of GLP-1 and GIP receptor-expressing cells in the DVC. In addition, we discuss how current advancements in single-cell transcriptomics, epigenetics, spatial transcriptomics, and circuit mapping techniques have the potential to further characterize incretin receptor circuits in the hindbrain.

Citing Articles

A single dorsal vagal complex circuit mediates the aversive and anorectic responses to GLP1R agonists.

Yacawych W, Wang Y, Zhou G, Hassan S, Kernodle S, Sass F bioRxiv. 2025; .

PMID: 39896596 PMC: 11785067. DOI: 10.1101/2025.01.21.634167.


A Cross-Species Atlas of the Dorsal Vagal Complex Reveals Neural Mediators of Cagrilintide's Effects on Energy Balance.

Ludwig M, Coester B, Gordian D, Hassan S, Tomlinson A, Toure M bioRxiv. 2025; .

PMID: 39868309 PMC: 11760743. DOI: 10.1101/2025.01.13.632726.


Dissociable hindbrain GLP1R circuits for satiety and aversion.

Huang K, Acosta A, Ghidewon M, McKnight A, Almeida M, Nyema N Nature. 2024; 632(8025):585-593.

PMID: 38987598 DOI: 10.1038/s41586-024-07685-6.


DPP-4 inhibitors sitagliptin and PF-00734,200 mitigate dopaminergic neurodegeneration, neuroinflammation and behavioral impairment in the rat 6-OHDA model of Parkinson's disease.

Yu S, Wang Y, Shen H, Bae E, Li Y, Sambamurti K Geroscience. 2024; 46(5):4349-4371.

PMID: 38563864 PMC: 11336009. DOI: 10.1007/s11357-024-01116-0.


Multiple NTS neuron populations cumulatively suppress food intake.

Qiu W, Hutch C, Wang Y, Wloszek J, Rucker R, Myers M Elife. 2023; 12.

PMID: 38059498 PMC: 10781422. DOI: 10.7554/eLife.85640.


References
1.
Adriaenssens A, Biggs E, Darwish T, Tadross J, Sukthankar T, Girish M . Glucose-Dependent Insulinotropic Polypeptide Receptor-Expressing Cells in the Hypothalamus Regulate Food Intake. Cell Metab. 2019; 30(5):987-996.e6. PMC: 6838660. DOI: 10.1016/j.cmet.2019.07.013. View

2.
Holt M, Richards J, Cook D, Brierley D, Williams D, Reimann F . Preproglucagon Neurons in the Nucleus of the Solitary Tract Are the Main Source of Brain GLP-1, Mediate Stress-Induced Hypophagia, and Limit Unusually Large Intakes of Food. Diabetes. 2018; 68(1):21-33. PMC: 6314470. DOI: 10.2337/db18-0729. View

3.
Smallwood S, Lee H, Angermueller C, Krueger F, Saadeh H, Peat J . Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity. Nat Methods. 2014; 11(8):817-820. PMC: 4117646. DOI: 10.1038/nmeth.3035. View

4.
Nitzan M, Karaiskos N, Friedman N, Rajewsky N . Gene expression cartography. Nature. 2019; 576(7785):132-137. DOI: 10.1038/s41586-019-1773-3. View

5.
NamKoong C, Kim M, Jang B, Lee Y, Cho Y, Choi H . Central administration of GLP-1 and GIP decreases feeding in mice. Biochem Biophys Res Commun. 2017; 490(2):247-252. DOI: 10.1016/j.bbrc.2017.06.031. View