Literature DB >> 7558688

Molecular mechanisms for passive and active transport of water.

T Zeuthen1.   

Abstract

Water crosses cell membranes by passive transport and by secondary active cotransport along with ions. While the first concept is well established, the second is new. The two modes of transport allow cellular H2O homeostasis to be viewed as a balance between H2O leaks and H2O pumps. Consequently, cells can be hyperosmolar relative to their surroundings during steady states. Under physiological conditions, cells from leaky epithelia may be hyperosmolar by roughly 5 mosm liter-1, under dilute conditions, hyperosmolarities up to 40 mosm liter-1 have been recorded. Most intracellular H2O is free to serve as solvent for small inorganic ions. The mechanism of transport across the membrane depends on how H2O interacts with the proteinaceous or lipoid pathways. Osmotic transport of H2O through specific H2O channels such as CHIP 28 is hydraulic if the pore is impermeable to the solute and diffusive if the pore is permeable. Cotransport of ions and H2O can be a result of conformational changes in proteins, which in addition to ion transport also translocate H2O bound to or occlude in the protein. A cellular model of a leaky epithelium based on H2O leaks and H2O pumps quantitatively predicts a number of so-far unexplained observations of H2O transport.

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Year:  1995        PMID: 7558688     DOI: 10.1016/s0074-7696(08)61554-5

Source DB:  PubMed          Journal:  Int Rev Cytol        ISSN: 0074-7696


  11 in total

Review 1.  Osmosensing by bacteria: signals and membrane-based sensors.

Authors:  J M Wood
Journal:  Microbiol Mol Biol Rev       Date:  1999-03       Impact factor: 11.056

2.  The human Na+-glucose cotransporter is a molecular water pump.

Authors:  A Meinild; D A Klaerke; D D Loo; E M Wright; T Zeuthen
Journal:  J Physiol       Date:  1998-04-01       Impact factor: 5.182

3.  The effect of a transmembrane osmotic flux on the ion concentration distribution in the immediate membrane vicinity measured by microelectrodes.

Authors:  P Pohl; S M Saparov; Y N Antonenko
Journal:  Biophys J       Date:  1997-04       Impact factor: 4.033

4.  Water does not flow across the tight junctions of MDCK cell epithelium.

Authors:  O Kovbasnjuk; J P Leader; A M Weinstein; K R Spring
Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

5.  Cotransport of water by the Na+/glucose cotransporter.

Authors:  D D Loo; T Zeuthen; G Chandy; E M Wright
Journal:  Proc Natl Acad Sci U S A       Date:  1996-11-12       Impact factor: 11.205

6.  Cotransport of H+, lactate and H2O by membrane proteins in retinal pigment epithelium of bullfrog.

Authors:  T Zeuthen; S Hamann; M la Cour
Journal:  J Physiol       Date:  1996-11-15       Impact factor: 5.182

7.  Isolation and characterization of NaCl-sensitive mutants of Caulobacter crescentus.

Authors:  Luiz Fernando G Zuleta; Valéria C S Italiani; Marilis V Marques
Journal:  Appl Environ Microbiol       Date:  2003-06       Impact factor: 4.792

Review 8.  Water-transporting proteins.

Authors:  Thomas Zeuthen
Journal:  J Membr Biol       Date:  2009-11-30       Impact factor: 1.843

9.  Mobility of ions, sugar, and water in the cytoplasm of Xenopus oocytes expressing Na(+)-coupled sugar transporters (SGLT1).

Authors:  Thomas Zeuthen; Emil Zeuthen; Dan A Klaerke
Journal:  J Physiol       Date:  2002-07-01       Impact factor: 5.182

10.  Poplar aquaporin PIP1;1 promotes Arabidopsis growth and development.

Authors:  Huani Leng; Cheng Jiang; Xueqin Song; Mengzhu Lu; Xianchong Wan
Journal:  BMC Plant Biol       Date:  2021-06-03       Impact factor: 4.215

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