Literature DB >> 10998665

Why should a clinician care about the molecular biology of transport?

A J Janecki1.   

Abstract

This review outlines the progress made over the last few years in three chosen areas of intestinal ion transport. In the field of intestinal secretion, research on the secretion of bicarbonate by pancreatic ducts and duodenal epithelia in cystic fibrosis revealed the crucial role of chloride channel (CFTR) in the control of activity of other transporters involved in bicarbonate secretion. In the area of intestinal absorption, studies on the regulation and physiologic roles of epithelial Na(+)/H(+) exchangers confirmed the suspected involvement of recycling in the acute regulation of NHE3 activity and resulted in formulation of new concepts for the roles of NHE3 and NHE2 in the gastrointestinal tract. Finally, the recent discovery of the first known viral enterotoxin revolutionized our understanding of pathomechanisms of secretory diarrhea during viral infections in humans. All of these findings are discussed in the context of their utility to the practicing gastroenterologist.

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Year:  2000        PMID: 10998665     DOI: 10.1007/s11894-000-0037-5

Source DB:  PubMed          Journal:  Curr Gastroenterol Rep        ISSN: 1522-8037


  56 in total

1.  Cystic fibrosis transmembrane conductance regulator currents in guinea pig pancreatic duct cells: inhibition by bicarbonate ions.

Authors:  C M O'Reilly; J P Winpenny; B E Argent; M A Gray
Journal:  Gastroenterology       Date:  2000-06       Impact factor: 22.682

2.  Ultrastructural changes in oxyntic cells associated with secretory function: a membrane-recycling hypothesis.

Authors:  T M Forte; T E Machen; J G Forte
Journal:  Gastroenterology       Date:  1977-10       Impact factor: 22.682

3.  Expression and distribution of the Na(+)-HCO(-)(3) cotransporter in human pancreas.

Authors:  C R Marino; V Jeanes; W F Boron; B M Schmitt
Journal:  Am J Physiol       Date:  1999-08

4.  Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA.

Authors:  J R Riordan; J M Rommens; B Kerem; N Alon; R Rozmahel; Z Grzelczak; J Zielenski; S Lok; N Plavsic; J L Chou
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

5.  CFTR upregulates the expression of the basolateral Na(+)-K(+)-2Cl(-) cotransporter in cultured pancreatic duct cells.

Authors:  H Shumaker; M Soleimani
Journal:  Am J Physiol       Date:  1999-12

6.  A functional CFTR protein is required for mouse intestinal cAMP-, cGMP- and Ca(2+)-dependent HCO3- secretion.

Authors:  U Seidler; I Blumenstein; A Kretz; D Viellard-Baron; H Rossmann; W H Colledge; M Evans; R Ratcliff; M Gregor
Journal:  J Physiol       Date:  1997-12-01       Impact factor: 5.182

7.  Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca2+-activated Cl- channel proteins.

Authors:  A D Gruber; R C Elble; H L Ji; K D Schreur; C M Fuller; B U Pauli
Journal:  Genomics       Date:  1998-12-01       Impact factor: 5.736

8.  Endosomal recycling of the Na+/H+ exchanger NHE3 isoform is regulated by the phosphatidylinositol 3-kinase pathway.

Authors:  K Kurashima; E Z Szabó; G Lukacs; J Orlowski; S Grinstein
Journal:  J Biol Chem       Date:  1998-08-14       Impact factor: 5.157

9.  CFTR channel insertion to the apical surface in rat duodenal villus epithelial cells is upregulated by VIP in vivo.

Authors:  N A Ameen; B Martensson; L Bourguinon; C Marino; J Isenberg; G E McLaughlin
Journal:  J Cell Sci       Date:  1999-03       Impact factor: 5.285

Review 10.  Regulation of Na+/glucose cotransporters.

Authors:  E M Wright; J R Hirsch; D D Loo; G A Zampighi
Journal:  J Exp Biol       Date:  1997-01       Impact factor: 3.312

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