Sorting of ion transport proteins in polarized cells

1993 ◽  
Vol 1993 (Supplement 17) ◽  
pp. 13-20 ◽  
Author(s):  
C. J. Gottardi ◽  
G. Pietrini ◽  
D. L. Roush ◽  
M. J. Caplan
1996 ◽  
Vol 18 (1-2) ◽  
pp. 23-28 ◽  
Author(s):  
H�l�ne Barbier-Brygoo ◽  
Sabine Zimmermann ◽  
S�bastien Thomine ◽  
Ian R. White ◽  
Paul Millner ◽  
...  

2019 ◽  
Vol 55 (87) ◽  
pp. 13152-13155
Author(s):  
Awatef Ben Tahar ◽  
Abdelkader Zebda ◽  
Jean-Pierre Alcaraz ◽  
Landry Gayet ◽  
Abderrahim Boualam ◽  
...  

This biomimetic membrane system of Na+/H+ transport proteins in a lipid bilayer supported by polyanaline has controllable electrogenic ion transport to function as a high-speed rechargeable biocapacitor for use in bioinspired biological engineering.


2010 ◽  
Vol 298 (1) ◽  
pp. C1-C10 ◽  
Author(s):  
Sascha Kopic ◽  
Michael Murek ◽  
John P. Geibel

The parietal cell is responsible for secreting concentrated hydrochloric acid into the gastric lumen. To fulfill this task, it is equipped with a broad variety of functionally coupled apical and basolateral ion transport proteins. The concerted scientific effort over the last years by a variety of researchers has provided us with the molecular identity of many of these transport mechanisms, thereby contributing to the clarification of persistent controversies in the field. This article will briefly review the current model of parietal cell physiology and ion transport in particular and will update the existing models of apical and basolateral transport in the parietal cell.


2014 ◽  
Vol 369 (1638) ◽  
pp. 20130102 ◽  
Author(s):  
Albrecht Schwab ◽  
Christian Stock

Cell migration is a central component of the metastatic cascade requiring a concerted action of ion channels and transporters (migration-associated transportome), cytoskeletal elements and signalling cascades. Ion transport proteins and aquaporins contribute to tumour cell migration and invasion among other things by inducing local volume changes and/or by modulating Ca 2+ and H + signalling. Targeting cell migration therapeutically bears great clinical potential, because it is a prerequisite for metastasis. Ion transport proteins appear to be attractive candidate target proteins for this purpose because they are easily accessible as membrane proteins and often overexpressed or activated in cancer. Importantly, a number of clinically widely used drugs are available whose anticipated efficacy as anti-tumour drugs, however, has now only begun to be evaluated.


2007 ◽  
Vol 44 (11) ◽  
pp. 1146-1156 ◽  
Author(s):  
Heather E. Hallen ◽  
Marianne Huebner ◽  
Shin-Han Shiu ◽  
Ulrich Güldener ◽  
Frances Trail

2004 ◽  
Vol 28 (4) ◽  
pp. 143-154 ◽  
Author(s):  
George R. Dubyak

The steady-state maintenance of highly asymmetric concentrations of the major inorganic cations and anions is a major function of both plasma membranes and the membranes of intracellular organelles. Homeostatic regulation of these ionic gradients is critical for most functions. Due to their charge, the movements of ions across biological membranes necessarily involves facilitation by intrinsic membrane transport proteins. The functional characterization and categorization of membrane transport proteins was a major focus of cell physiological research from the 1950s through the 1980s. On the basis of these functional analyses, ion transport proteins were broadly divided into two classes: channels and carrier-type transporters (which include exchangers, cotransporters, and ATP-driven ion pumps). Beginning in the mid-1980s, these functional analyses of ion transport and homeostasis were complemented by the cloning of genes encoding many ion channels and transporter proteins. Comparison of the predicted primary amino acid sequences and structures of functionally similar ion transport proteins facilitated their grouping within families and superfamilies of structurally related membrane proteins. Postgenomics research in ion transport biology increasingly involves two powerful approaches. One involves elucidation of the molecular structures, at the atomic level in some cases, of model ion transport proteins. The second uses the tools of cell biology to explore the cell-specific function or subcellular localization of ion transport proteins. This review will describe how these approaches have provided new, and sometimes surprising, insights regarding four major questions in current ion transporter research. 1) What are the fundamental differences between ion channels and ion transporters? 2) How does the interaction of an ion transport protein with so-called adapter proteins affect its subcellular localization or regulation by various intracellular signal transduction pathways? 3) How does the specific lipid composition of the local membrane microenvironment modulate the function of an ion transport protein? 4) How can the basic functional properties of a ubiquitously expressed ion transport protein vary depending on the cell type in which it is expressed?


1983 ◽  
Vol 6 (1) ◽  
pp. 419-446 ◽  
Author(s):  
S M Goldin ◽  
E G Moczydlowski ◽  
D M Papazian

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