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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9343792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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