4.7 Article

theLiTE™: A Screening Platform to Identify Compounds that Reinforce Tight Junctions

期刊

FRONTIERS IN PHARMACOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.752787

关键词

PAR-6; epithelial cells; tight junctions; quercetin; myricetin; polarity (cell)

资金

  1. Thelial Technologies S.A.
  2. European Research Council (ERC) [745175]

向作者/读者索取更多资源

Tight junctions are formed by proteins that seal the intercellular space and control the permeability of epithelia. This study focuses on finding compounds that reinforce the epithelial barrier and developed a screening platform to identify compounds that modulate the expression of Par-6, a protein involved in tight junction assembly. Six compounds were tested and two of them (myricetin and quercetin) were shortlisted for further development.
Tight junctions (TJ) are formed by transmembrane and intracellular proteins that seal the intercellular space and control selective permeability of epithelia. Integrity of the epithelial barrier is central to tissue homeostasis and barrier dysfunction has been linked to many pathological conditions. TJ support the maintenance of cell polarity through interactions with the Par complex (Cdc42-Par-6-Par-3-aPKC) in which Par-6 is an adaptor and links the proteins of the complex together. Studies have shown that Par-6 overexpression delays the assembly of TJ proteins suggesting that Par-6 negatively regulates TJ assembly. Because restoring barrier integrity is of key therapeutic and prophylactic value, we focus on finding compounds that have epithelial barrier reinforcement properties; we developed a screening platform (theLiTE (TM)) to identify compounds that modulate Par-6 expression in follicular epithelial cells from Par-6-GFP Drosophila melanogaster egg chambers. Hits identified were then tested whether they improve epithelial barrier function, using measurements of transepithelial electrical resistance (TEER) or dye efflux to evaluate paracellular permeability. We tested 2,400 compounds, found in total 10 hits. Here we present data on six of them: the first four hits allowed us to sequentially build confidence in theLiTE (TM) and two compounds that were shortlisted for further development (myricetin and quercetin). We selected quercetin due to its clinical and scientific validation as a compound that regulates TJ; food supplement formulated on the basis of this discovery is currently undergoing clinical evaluation in gastroesophageal reflux disease (GERD) sufferers.

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