Am J Physiol Cell Physiol Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Cell Physiol 295: C954-C965, 2008. First published August 6, 2008; doi:10.1152/ajpcell.00009.2008
0363-6143/08 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
295/4/C954    most recent
00009.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Balasubramanian, L.
Right arrow Articles by Lo, C.-M.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Balasubramanian, L.
Right arrow Articles by Lo, C.-M.

METHODS IN CELL PHYSIOLOGY

Impedance analysis of renal vascular smooth muscle cells

Lavanya Balasubramanian,1 Kay-Pong Yip,1 Tai-Hsin Hsu,3 and Chun-Min Lo2

1Department of Molecular Pharmacology and Physiology and 2Department of Physics, University of South Florida, Tampa, Florida; and 3Department of Physics, National Cheng Kung University, Tainan, Taiwan

Submitted 8 January 2008 ; accepted in final form 31 July 2008

Impedance of renal vascular smooth muscle cells (VSMCs) cultured on microelectrodes was measured by electric cell-substrate impedance sensing. Changes in measured impedance as a function of frequency were compared with the calculated values obtained from an extended cell-electrode model to estimate the junctional resistance, distance between the ventral cell surface and the substratum, and apical and basolateral membrane capacitances of renal VSMCs. This cell-electrode model was derived to accommodate the slender and rectangular shape of VSMCs. The calculated changes in impedance (Zcal) based on the model agreed well with the experimental measurement (Zexp), and the percentage error defined as |(Zcal Zexp)/Zexp| was 1.0%. To test the sensitivity of the new model for capturing changes in cell-cell and cell-substrate interactions induced by changes in cellular environment, we then applied this model to analyze timpedance changes induced by an integrin binding peptide in renal VSMCs. Our result demonstrates that integrin binding peptide decreases junctional resistance between cells, increases the distance between the basolateral cell surface and substratum, and increases the apical membrane capacitance, whereas the basolateral membrane capacitance stays relatively stable. This model provides a generic approach for impedance analysis of cell layers composed of slender, rectangular cells.

electric cell-substrate impedance sensing; cell attachment; cell adhesion; extracellular matrix; integrin



Address for reprint requests and other correspondence: C.-M. Lo, Dept. of Physics, College of Arts and Sciences, Univ. of South Florida, 4202 East Fowler Ave., PHY303, Tampa, FL 33620-5700 (e-mail: cmlo{at}cas.usf.edu)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2008 by the American Physiological Society.