Imaging viscosity of intragranular mucin matrix in cystic fibrosis cells

Sebastian Requena1, Olga Ponomarchuk2,3, Marlius Castillo4

  • 1University of North Texas Health Science Center, Department of Microbiology, Immunology & Genetics, Fort Worth, TX, 76107, USA.

Scientific Reports
|December 3, 2017
PubMed

Insights

Researchers developed a new method to measure mucus viscosity inside live cells. This technique visualizes mucin granule viscosity, aiding the study of respiratory diseases like cystic fibrosis.

Area of Science:

  • Biophysics
  • Cell Biology
  • Respiratory Medicine

Background:

  • Mucus viscosity is crucial in respiratory diseases such as cystic fibrosis.
  • Existing methods cannot assess mucin granule rheology in living cells.

Purpose of the Study:

  • To develop a novel method for quantifying intragranular mucin viscosity in live cells.
  • To enable real-time analysis of mucus properties within individual mucin granules.

Main Methods:

  • Utilized a BODIPY-based molecular rotor and fluorescence lifetime imaging microscopy (FLIM).
  • Applied the method to differentiated primary bronchial epithelial cells.
  • Quantitatively visualized viscosity in a large population of individual granules.

Main Results:

  • Successfully visualized and quantified the viscosity of intragranular mucin matrices.
  • Demonstrated the ability to assess rheological properties at the single-granule level.
  • Established a new tool for studying mucus in live respiratory cells.

Conclusions:

  • This study presents the first method to measure mucin granule viscosity in live cells.
  • The technique offers new insights into the role of mucus rheology in respiratory disease pathogenesis.
  • Provides a valuable platform for future research on mucin dynamics and related diseases.