AI Article Synopsis

  • The intestinal epithelium plays a crucial role in nutrient transport and barrier protection, and any impairment in its function can lead to various diseases and affect other bodily functions.
  • Different in vitro cell culture models, like Caco-2 cells, fall short in mimicking the complex interactions of the natural intestinal epithelium, which presents challenges in the study of epithelial transport.
  • This study highlights an innovative 3D culture system for Caco-2 cells and introduces the use of the Ussing chamber to effectively measure transporter function, specifically focusing on serotonin transport.

Article Abstract

The intestinal epithelium has important transport and barrier functions that play key roles in normal physiological functions of the body while providing a barrier to foreign particles. Impaired epithelial transport (ion, nutrient, or drugs) has been associated with many diseases and can have consequences that extend beyond the normal physiological functions of the transporters, such as by influencing epithelial integrity and the gut microbiome. Understanding the function and regulation of transport proteins is critical for the development of improved therapeutic interventions. The biggest challenge in the study of epithelial transport is developing a suitable model system that recapitulates important features of the native intestinal epithelial cells. Several in vitro cell culture models, such as Caco-2, T-84, and HT-29-Cl.19A cells are typically used in epithelial transport research. These cell lines represent a reductionist approach to modeling the epithelium and have been used in many mechanistic studies, including their examination of epithelial-microbial interactions. However, cell monolayers do not accurately reflect cell-cell interactions and the in vivo microenvironment. Cells grown in 3D have shown to be promising models for drug permeability studies. We show that Caco-2 cells in 3D can be used to study epithelial transporters. It is also important that studies in Caco-2 cells are complemented with other models to rule out cell specific effects and to take into account the complexity of the native intestine. Several methods have been previously used to assess the functionality of transporters, such as everted sac and uptake in isolated epithelial cells or in isolated plasma membrane vesicles. Taking into consideration the challenges in the field with respect to models and the measurement of transport function, we demonstrate here a protocol to grow Caco-2 cells in 3D and describe the use of an Ussing chamber as an effective approach to measure serotonin transport, such as in intact polarized intestinal epithelia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408935PMC
http://dx.doi.org/10.3791/55304DOI Listing

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