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Identification of Intestinal NaCl Absorptive-Anion Secretory Cells: Potential Functional Significance.
Donowitz, Mark; Sarker, Rafiquel; Lin, Ruxian; McNamara, George; Tse, Chung Ming; Singh, Varsha.
Afiliação
  • Donowitz M; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Sarker R; Department of Physiology, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Lin R; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • McNamara G; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Tse CM; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Singh V; Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD, United States.
Front Physiol ; 13: 892112, 2022.
Article em En | MEDLINE | ID: mdl-35928564
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Physiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Front Physiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos
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