Quantitative Analysis of Delta-like 1 Membrane Dynamics Elucidates the Role of Contact Geometry on Notch Signaling.

Cell Rep

Department of Biochemistry and Molecular Biology, Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel. Electronic address:

Published: January 2016

AI Article Synopsis

  • Notch signaling is crucial for coordinating cell differentiation across various organisms, but the impact of receptor and ligand distribution on signaling is not well understood.
  • By using live-cell imaging and mathematical modeling, researchers studied the behavior of the Notch ligand Delta-like 1 (Dll1) in mammalian cells, revealing significant variability in its diffusion rates among different cells.
  • The findings indicate that the dynamics of membrane distribution and cell shape can significantly influence cell-to-cell signaling, highlighting the importance of these factors in biological processes.

Article Abstract

Notch signaling is ubiquitously used to coordinate differentiation between adjacent cells across metazoans. Whereas Notch pathway components have been studied extensively, the effect of membrane distribution and dynamics of Notch receptors and ligands remains poorly understood. It is also unclear how cellular morphology affects these distributions and, ultimately, the signaling between cells. Here, we combine live-cell imaging and mathematical modeling to address these questions. We use a FRAP-TIRF assay to measure the diffusion and endocytosis rates of Delta-like 1 (Dll1) in mammalian cells. We find large cell-to-cell variability in the diffusion coefficients of Dll1 measured in single cells within the same population. Using a simple reaction-diffusion model, we show how membrane dynamics and cell morphology affect cell-cell signaling. We find that differences in the diffusion coefficients, as observed experimentally, can dramatically affect signaling between cells. Together, these results elucidate how membrane dynamics and cellular geometry can affect cell-cell signaling.

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Source
http://dx.doi.org/10.1016/j.celrep.2015.12.040DOI Listing

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