Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

G Protein-coupled Receptors01:15

G Protein-coupled Receptors

11.2K
G Protein-Coupled Receptors or GPCRs are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to sensory stimuli such as light, odors, hormones, cytokines, or neurotransmitters.
GPCRs are also called heptahelical, 7TM, or serpentine receptors, and consist of seven (H1-H7) transmembrane alpha-helices that span the bilayer to form a cylindrical core. The transmembrane helices are connected by three extracellular loops and three...
11.2K
G-protein Coupled Receptors01:21

G-protein Coupled Receptors

115.4K
G-protein coupled receptors are ligand binding receptors that indirectly affect changes in the cell. The actual receptor is a single polypeptide that transverses the cell membrane seven times creating intracellular and extracellular loops. The extracellular loops create a ligand specific pocket which binds to neurotransmitters or hormones. The intracellular loops holds onto the G-protein.
115.4K
Signal Transduction: Overview01:26

Signal Transduction: Overview

8.2K
Cells respond to many types of information, often through receptor proteins positioned on the membrane. They respond to chemical signals, such as hormones, neurotransmitters, and other signaling molecules, initiating a series of molecular reactions to produce an appropriate response. This is called signal transduction. Cells also coordinate different responses elicited by the same signaling molecule via mediators, allowing molecular cross-talk.
Typically, signal transduction involves three...
8.2K
Transducer Mechanism: G Protein–Coupled Receptors01:30

Transducer Mechanism: G Protein–Coupled Receptors

1.8K
G Protein–Coupled Receptors (GPCRs) are membrane-bound receptors that transiently associate with heterotrimeric G proteins and induce an appropriate response to various stimuli. GPCRs regulate critical physiological pathways and are excellent drug targets for treating diseases such as diabetes, cancer, obesity, depression, or Alzheimer's. Nearly 35% of approved drugs implement their therapeutic effects by selectively interacting with specific GPCRs.
GPCRs are also called heptahelical,...
1.8K
Overview of Cell Signaling01:23

Overview of Cell Signaling

20.0K
Despite the protective membrane that separates a cell from the environment, cells need the ability to detect and respond to environmental changes. Additionally, cells often need to communicate with one another. Unicellular and multicellular organisms use a variety of cell signaling mechanisms to communicate with the environment.
Cells respond to many types of information, often through receptor proteins positioned on the membrane. For example, skin cells respond to and transmit touch...
20.0K
Overview of Cell-Matrix Interactions01:24

Overview of Cell-Matrix Interactions

7.0K
The extracellular matrix or ECM holds cells together to form a tissue and allows the cells within the tissue to communicate. ECM comprises proteins such as fibronectin, collagen, laminin, etc. The most abundant protein in this space is collagen. Collagen fibers are interwoven with carbohydrate-containing protein molecules called proteoglycans. ECM allows cell migration and provides a structural scaffold at cell adhesion that anchors the cell when the extracellular matrix proteins interact with...
7.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Diagnostic Value of LINC00426 in Type 2 Diabetes and Diabetic Kidney Disease and its Regulatory Effects on Renal Cells.

Journal of visualized experiments : JoVE·2026
Same author

Antifibrotic Effects of Yi-Qi-Jian-Pi-Xiao-Yu Formula in Kidney via HIF1A-Driven M1 Macrophage Polarization.

Phytochemical analysis : PCA·2026
Same author

Diphenoquinone-Based Covalent Organic Frameworks for Efficient H<sub>2</sub>O<sub>2</sub> Production via Photothermal Synergistic Catalysis.

Angewandte Chemie (International ed. in English)·2026
Same author

Clinical efficacy of acupuncture for women with PCOS undergoing IVF/ICSI: a meta-analysis of randomized controlled trials.

Frontiers in endocrinology·2026
Same author

Ovarian endometrioid carcinoma with sex cord-like features: a case report with genomic and transcriptomic analyses and literature review.

Frontiers in oncology·2026
Same author

A Novel Clinical Classification for Atlantoaxial Dislocation: Based on Surgical Outcomes of 1032 Cases.

Spine·2026

Related Experiment Video

Updated: Jun 3, 2025

Detection of Ligand-activated G Protein-coupled Receptor Internalization by Confocal Microscopy
10:24

Detection of Ligand-activated G Protein-coupled Receptor Internalization by Confocal Microscopy

Published on: April 9, 2017

10.7K

CellMsg: graph convolutional networks for ligand-receptor-mediated cell-cell communication analysis.

Hong Xia1, Boya Ji1, Debin Qiao2

  • 1College of Computer Science and Electronic Engineering, Hunan University, Changsha 410082, China.

Briefings in Bioinformatics
|January 12, 2025
PubMed
Summary

CellMsg is a new computational tool that identifies ligand-receptor interactions (LRIs) and measures cell-cell communication (CCC) strength from single-cell RNA sequencing data, offering a robust method for studying tumoral tissues.

Keywords:
cell–cell communicationsgraph convolutional networksligand–receptor interactionsthree-point estimation method

More Related Videos

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy
09:24

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Published on: January 30, 2020

7.9K
High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy
15:13

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Published on: July 25, 2014

11.4K

Related Experiment Videos

Last Updated: Jun 3, 2025

Detection of Ligand-activated G Protein-coupled Receptor Internalization by Confocal Microscopy
10:24

Detection of Ligand-activated G Protein-coupled Receptor Internalization by Confocal Microscopy

Published on: April 9, 2017

10.7K
Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy
09:24

Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

Published on: January 30, 2020

7.9K
High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy
15:13

High-resolution Spatiotemporal Analysis of Receptor Dynamics by Single-molecule Fluorescence Microscopy

Published on: July 25, 2014

11.4K

Area of Science:

  • Computational biology
  • Genomics
  • Cancer research

Background:

  • Cell-cell communications (CCCs) are crucial in tumoral tissues, influencing differentiation, invasion, metastasis, and drug resistance.
  • Traditional experimental methods for inferring CCCs are inefficient for large datasets.

Purpose of the Study:

  • To develop a computational framework, CellMsg, for efficient inference of CCCs.
  • To identify high-confidence ligand-receptor interactions (LRIs) and quantify CCC strength.

Main Methods:

  • CellMsg utilizes multimodal features and graph convolutional networks to identify LRIs.
  • It employs a three-point estimation method combining LRIs and single-cell RNA-seq data to measure CCC strength.
  • Performance was validated using benchmark LRI datasets, cross-validation, and molecular docking.

Main Results:

  • CellMsg accurately identifies high-confidence LRIs with superior prediction performance and robustness compared to existing methods.
  • Identified LRIs were validated through molecular docking.
  • Analysis of human melanoma tissue revealed intercellular crosstalk among seven cell types.

Conclusions:

  • CellMsg provides a reliable LRI database and an effective CCC strength evaluation method for single-cell RNA-seq data.
  • This computational tool facilitates the deciphering of intercellular communications in biological systems.
  • CellMsg is publicly available for research use.