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Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance

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 popu...

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Autores principales: Donowitz, Mark, Sarker, Rafiquel, Lin, Ruxian, McNamara, George, Tse, Chung Ming, Singh, Varsha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343792/
https://www.ncbi.nlm.nih.gov/pubmed/35928564
http://dx.doi.org/10.3389/fphys.2022.892112
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author Donowitz, Mark
Sarker, Rafiquel
Lin, Ruxian
McNamara, George
Tse, Chung Ming
Singh, Varsha
author_facet Donowitz, Mark
Sarker, Rafiquel
Lin, Ruxian
McNamara, George
Tse, Chung Ming
Singh, Varsha
author_sort Donowitz, Mark
collection PubMed
description 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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spelling pubmed-93437922022-08-03 Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance Donowitz, Mark Sarker, Rafiquel Lin, Ruxian McNamara, George Tse, Chung Ming Singh, Varsha Front Physiol Physiology 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. Frontiers Media S.A. 2022-07-19 /pmc/articles/PMC9343792/ /pubmed/35928564 http://dx.doi.org/10.3389/fphys.2022.892112 Text en Copyright © 2022 Donowitz, Sarker, Lin, McNamara, Tse and Singh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Donowitz, Mark
Sarker, Rafiquel
Lin, Ruxian
McNamara, George
Tse, Chung Ming
Singh, Varsha
Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title_full Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title_fullStr Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title_full_unstemmed Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title_short Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance
title_sort identification of intestinal nacl absorptive-anion secretory cells: potential functional significance
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9343792/
https://www.ncbi.nlm.nih.gov/pubmed/35928564
http://dx.doi.org/10.3389/fphys.2022.892112
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