ICELLNET

ICELLNET infers and quantifies cell–cell communication from single or multiple cell-based transcriptomic profiles by mapping ligand–receptor interactions to dissect intercellular signaling.


Key Features:

  • Expert-Curated Ligand–Receptor Database: An original expert-curated database catalogs ligand–receptor interactions and accounts for the expression of multiple subunits.
  • Quantification of Communication Scores: Computes quantitative communication scores between cell populations to assess interaction strength and significance.
  • Integration with Reference Cell Types: Connects a cell population of interest to 31 reference human cell types sourced from BioGPS.
  • Compatibility with Single or Multiple Profiles: Applies to single or multiple cell-based transcriptomic profiles for comparative and context-specific analyses.
  • Three Visualization Modes: Provides three distinct visualization modes to support biological interpretation of inferred communication networks.

Scientific Applications:

  • Breast cancer-associated fibroblast (CAF) analysis: Uncovered nuanced differences in intercellular communication among subsets of CAFs in breast cancer.
  • Dendritic cell IL-10 autocrine signaling: Identified autocrine IL-10 signaling as a regulator of human dendritic cell communication with up to 12 other cell types, with four interactions experimentally validated.

Methodology:

Uses an expert-curated ligand–receptor database that accounts for multi-subunit expression, quantifies communication scores between cell populations, integrates profiles with 31 BioGPS reference human cell types, and presents results via three visualization modes.

Topics

Details

Tool Type:
library
Programming Languages:
R
Added:
1/18/2021
Last Updated:
2/1/2021

Operations

Data Inputs & Outputs

Publications

Noël F, Massenet-Regad L, Carmi-Levy I, Cappuccio A, Grandclaudon M, Trichot C, Kieffer Y, Mechta-Grigoriou F, Soumelis V. ICELLNET: a transcriptome-based framework to dissect intercellular communication. Unknown Journal. 2020. doi:10.1101/2020.03.05.976878.