AI Article Synopsis

  • The research uses human enteroids in both undifferentiated and differentiated states to study enterocyte populations that mirror the intestinal structure.
  • The focus is on a specific group of enterocytes transitioning from crypt to villus, which express key transporters (NHE3, DRA, CFTR) that interact and influence their functions in sodium absorption and anion secretion.
  • Insights from this study could lead to new drug development strategies aimed at improving intestinal transport and addressing disorders like diarrhea and constipation.

Article Abstract

Use of human enteroids studied in the undifferentiated and differentiated state that mimic the intestinal crypt and villus, respectively, has allowed studies of multiple enterocyte populations, including a large population of enterocytes that are transitioning from the crypt to the villus. This population expresses NHE3, DRA, and CFTR, representing a combination of Na absorptive and anion secretory functions. In this cell population, these three transporters physically interact, which affects their baseline and regulated activities. A study of this cell population and differentiated Caco-2 cells transduced with NHE3 and endogenously expressing DRA and CFTR has allowed an understanding of previous studies in which cAMP seemed to stimulate and inhibit DRA at the same time. Understanding the contributions of these cells to overall intestinal transport function as part of the fasting and post-prandial state and their contribution to the pathophysiology of diarrheal diseases and some conditions with constipation will allow new approaches to drug development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343792PMC
http://dx.doi.org/10.3389/fphys.2022.892112DOI Listing

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