article · 11/02/2026
Probing and modeling cell-cell communication in 2D biomimetic tissues
Résumé
In tissues, cells in direct physical contact with each other can exchange ions or molecules via protein clusters called gap junctions that form channels across the membranes of adjacent cells. Here, we use a simplified biomimetic approach, coupled with theoretical modeling, to unravel the physical mechanisms controlling such transport. Tissues are mimicked with 2D hexagonal networks of monodisperse aqueous droplets connected by lipid membranes called Droplet Interface Bilayers (DIBs), decorated with α-Hemolysin (αHL) transmembrane proteins forming nanopores through heptamerization in the membrane. The diffusion of calcein across 2D DIB networks is thoroughly studied using epifluorescence microscopy at various αHL concentrations. The results are successfully confronted with a Continuous Time Random Walk model in hexagonal networks, with an average waiting time increasing nonlinearly with the concentration of pore monomers.
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Vincent, C.-M., Ravindran, S., Prevost, A.-M., Pontani, L.-L., Bénichou, O., & Wandersman, E. (2026). Probing and modeling cell-cell communication in 2D biomimetic tissues. Soft Matter. https://doi.org/DOI https://doi.org/10.1039/D5SM01072A@article{Vincent2026_485,
author = {Vincent, Cécile Marie and Ravindran, Sapna and Prevost, Alexis Michel and Pontani, Léa-Laetitia and Bénichou, Olivier and Wandersman, Elie},
year = {2026},
month = {2},
title = {Probing and modeling cell-cell communication in 2D biomimetic tissues},
journal = {Soft Matter},
abstract = {In tissues, cells in direct physical contact with each other can exchange ions or molecules via protein clusters called gap junctions that form channels across the membranes of adjacent cells. Here, we use a simplified biomimetic approach, coupled with theoretical modeling, to unravel the physical mechanisms controlling such transport. Tissues are mimicked with 2D hexagonal networks of monodisperse aqueous droplets connected by lipid membranes called Droplet Interface Bilayers (DIBs), decorated with α-Hemolysin (αHL) transmembrane proteins forming nanopores through heptamerization in the membrane. The diffusion of calcein across 2D DIB networks is thoroughly studied using epifluorescence microscopy at various αHL concentrations. The results are successfully confronted with a Continuous Time Random Walk model in hexagonal networks, with an average waiting time increasing nonlinearly with the concentration of pore monomers.},
doi = {DOI https://doi.org/10.1039/D5SM01072A},
}TY - JOUR
AU - Vincent, Cécile Marie
AU - Ravindran, Sapna
AU - Prevost, Alexis Michel
AU - Pontani, Léa-Laetitia
AU - Bénichou, Olivier
AU - Wandersman, Elie
PY - 2026
DA - 2026/02/11
TI - Probing and modeling cell-cell communication in 2D biomimetic tissues
JO - Soft Matter
AB - In tissues, cells in direct physical contact with each other can exchange ions or molecules via protein clusters called gap junctions that form channels across the membranes of adjacent cells. Here, we use a simplified biomimetic approach, coupled with theoretical modeling, to unravel the physical mechanisms controlling such transport. Tissues are mimicked with 2D hexagonal networks of monodisperse aqueous droplets connected by lipid membranes called Droplet Interface Bilayers (DIBs), decorated with α-Hemolysin (αHL) transmembrane proteins forming nanopores through heptamerization in the membrane. The diffusion of calcein across 2D DIB networks is thoroughly studied using epifluorescence microscopy at various αHL concentrations. The results are successfully confronted with a Continuous Time Random Walk model in hexagonal networks, with an average waiting time increasing nonlinearly with the concentration of pore monomers.
DO - DOI https://doi.org/10.1039/D5SM01072A
ER -