Cell migration is crucial for processes such as immune defense, wound healing, or the formation of tumor metastases. Typically, migrating cells are polarized within the plane of movement with lamellipodium and cell body representing the front and rear of the cell, respectively. Here, we address the question of whether this polarization also extends to the distribution of ion transporters such as Na+/H+ exchanger (NHE) and anion exchanger in the plasma membrane of migrating cells. Both transporters are required for locomotion of renal epithelial (Madin-Darby canine kidney, MDCK-F) cells and human melanoma cells since their blockade reduces the rate of migration in a dose-dependent manner. Inhibition of migration of MDCK-F cells by NHE blockers is accompanied by a decrease of pHi. However, when cells are acidified with weak organic acids, migration of MDCK-F cells is normal despite an even more pronounced decrease of pHi. Under these conditions, NHE activity is increased so that cells are swelling due to the accumulation of organic anions and Na+. When exclusively applied to the lamellipodium, blockers of NHE or anion exchange inhibit migration of MDCK-F cells as effectively as when applied to the entire cell surface. When they are directed to the cell body, migration is not affected. These data are confirmed immunocytochemically in that the anion exchanger AE2 is concentrated at the front of MDCK-F cells. Our findings show that NHE and anion exchanger are distributed in a polarized way in migrating cells. They are consistent with important contributions of both transporters to protrusion of the lamellipodium via solute uptake and consequent volume increase at the front of migrating cells.
Skip Nav Destination
Article navigation
1 May 2000
Article|
May 01 2000
Polarization of Na+/H+ and Cl−/Hco 3− Exchangers in Migrating Renal Epithelial Cells
Magnus Klein,
Magnus Klein
aPhysiologisches Institut, D-97070 Würzburg, Germany
Search for other works by this author on:
Ponke Seeger,
Ponke Seeger
aPhysiologisches Institut, D-97070 Würzburg, Germany
Search for other works by this author on:
Barbara Schuricht,
Barbara Schuricht
aPhysiologisches Institut, D-97070 Würzburg, Germany
Search for other works by this author on:
Seth L. Alper,
Seth L. Alper
bDepartments of Medicine and Cell Biology, Harvard Medical School and Molecular Medicine and Renal Units, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215
Search for other works by this author on:
Albrecht Schwab
Albrecht Schwab
aPhysiologisches Institut, D-97070 Würzburg, Germany
Search for other works by this author on:
Magnus Klein
aPhysiologisches Institut, D-97070 Würzburg, Germany
Ponke Seeger
aPhysiologisches Institut, D-97070 Würzburg, Germany
Barbara Schuricht
aPhysiologisches Institut, D-97070 Würzburg, Germany
Seth L. Alper
bDepartments of Medicine and Cell Biology, Harvard Medical School and Molecular Medicine and Renal Units, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215
Albrecht Schwab
aPhysiologisches Institut, D-97070 Würzburg, Germany
Drs. Klein and Seeger contributed equally to this work and should be considered co-first authors.
Abbreviations used in this paper: DIDS, 4,4′-diisothiocyanate-stilbene-2,2′-disulfonic acid; EIPA, ethylisopropylamiloride; MDCK-F cells, Madin-Darby canine kidney cells; NHE, Na+/H+ exchanger.
Received:
December 29 1999
Revision Requested:
March 13 2000
Accepted:
March 20 2000
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Gen Physiol (2000) 115 (5): 599–608.
Article history
Received:
December 29 1999
Revision Requested:
March 13 2000
Accepted:
March 20 2000
Citation
Magnus Klein, Ponke Seeger, Barbara Schuricht, Seth L. Alper, Albrecht Schwab; Polarization of Na+/H+ and Cl−/Hco 3− Exchangers in Migrating Renal Epithelial Cells . J Gen Physiol 1 May 2000; 115 (5): 599–608. doi: https://doi.org/10.1085/jgp.115.5.599
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
ATP Dependence of the ICl, swell Channel Varies with Rate of Cell Swelling : Evidence for Two Modes of Channel Activation
J Gen Physiol (March,1999)
Recombinant pICln Forms Highly Cation-selective Channels when Reconstituted into Artificial and Biological Membranes
J Gen Physiol (December,1998)
Deuterium Isotope Effects on Permeation and Gating of Proton Channels in Rat Alveolar Epithelium
J Gen Physiol (April,1997)
Email alerts
Advertisement