Probing and modeling cell-cell communication in 2D biomimetic tissues

Fuente: arXiv
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Autori principali: Vincent, Cécile Marie, Ravindran, Sapna, Prevost, Alexis Michel, Pontani, Léa-Laetitia, Bénichou, Olivier, Wandersman, Elie
Natura: Preprint
Pubblicazione: 2025
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author Vincent, Cécile Marie
Ravindran, Sapna
Prevost, Alexis Michel
Pontani, Léa-Laetitia
Bénichou, Olivier
Wandersman, Elie
author_facet Vincent, Cécile Marie
Ravindran, Sapna
Prevost, Alexis Michel
Pontani, Léa-Laetitia
Bénichou, Olivier
Wandersman, Elie
contents 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 ($α$HL) 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 $α$HL 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.
format Preprint
id arxiv_https___arxiv_org_abs_2510_21474
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Probing and modeling cell-cell communication in 2D biomimetic tissues
Vincent, Cécile Marie
Ravindran, Sapna
Prevost, Alexis Michel
Pontani, Léa-Laetitia
Bénichou, Olivier
Wandersman, Elie
Soft Condensed Matter
Biological Physics
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 ($α$HL) 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 $α$HL 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.
title Probing and modeling cell-cell communication in 2D biomimetic tissues
topic Soft Condensed Matter
Biological Physics
url https://arxiv.org/abs/2510.21474