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A noninvasive fluorescence imaging-based platform measures 3D anisotropic extracellular diffusion

  • Peng Chen
  • , Xun Chen
  • , R. Glenn Hepfer
  • , Brooke J. Damon
  • , Changcheng Shi
  • , Jenny J. Yao
  • , Matthew C. Coombs
  • , Michael J. Kern
  • , Tong Ye*
  • , Hai Yao*
  • *Corresponding author for this work
  • Clemson University
  • Medical University of South Carolina
  • CAS - Ningbo Institute of Material Technology and Engineering
  • Harvard University

Research output: Contribution to journalArticlepeer-review

Abstract

Diffusion is a major molecular transport mechanism in biological systems. Quantifying direction-dependent (i.e., anisotropic) diffusion is vitally important to depicting how the three-dimensional (3D) tissue structure and composition affect the biochemical environment, and thus define tissue functions. However, a tool for noninvasively measuring the 3D anisotropic extracellular diffusion of biorelevant molecules is not yet available. Here, we present light-sheet imaging-based Fourier transform fluorescence recovery after photobleaching (LiFT-FRAP), which noninvasively determines 3D diffusion tensors of various biomolecules with diffusivities up to 51 µm2 s−1, reaching the physiological diffusivity range in most biological systems. Using cornea as an example, LiFT-FRAP reveals fundamental limitations of current invasive two-dimensional diffusion measurements, which have drawn controversial conclusions on extracellular diffusion in healthy and clinically treated tissues. Moreover, LiFT-FRAP demonstrates that tissue structural or compositional changes caused by diseases or scaffold fabrication yield direction-dependent diffusion changes. These results demonstrate LiFT-FRAP as a powerful platform technology for studying disease mechanisms, advancing clinical outcomes, and improving tissue engineering.

Original languageEnglish
Article number1913
JournalNature Communications
Volume12
Issue number1
DOIs
StatePublished - 1 Dec 2021
Externally publishedYes

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