AI Article Synopsis

  • The study investigates how disruptions in cell-matrix adhesion affect the permeability of colon cells.
  • Researchers observed that adding Aquamin®, a multi-mineral supplement, improved the expression of proteins that help with cell-matrix adhesion and increased transepithelial electrical resistance (TEER), indicating better barrier function.
  • A blocking antibody targeting a specific protein decreased TEER, especially when Aquamin® was not present, highlighting the importance of cell-matrix interactions in maintaining intestinal barrier integrity.

Article Abstract

The importance of cell-matrix adhesion to barrier control in the colon is unclear. The goals of the present study were to: (i) determine if disruption of colon epithelial cell interactions with the extracellular matrix alters permeability control measurement and (ii) determine if increasing the elaboration of protein components of cell-matrix adhesion complexes can mitigate the effects of cell-matrix disruption. Human colon organoids were interrogated for transepithelial electrical resistance (TEER) under control conditions and in the presence of Aquamin®, a multi-mineral product. A function-blocking antibody directed at the C-terminal region of the laminin α chain was used in parallel. The effects of Aquamin® on cell-matrix adhesion protein expression were determined in a proteomic screen and by Western blotting. Aquamin® increased the expression of multiple basement membrane, hemidesmosomal and focal adhesion proteins as well as keratin 8 and 18. TEER values were higher in the presence of Aquamin® than they were under control conditions. The blocking antibody reduced TEER values under both conditions but was most effective in the absence of Aquamin®, where expression of cell-matrix adhesion proteins was lower to begin with. These findings provide evidence that cell-matrix interactions contribute to barrier control in the colon.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8960989PMC
http://dx.doi.org/10.3389/fmed.2022.838975DOI Listing

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