help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on October 15, 2004.
doi:10.1529/biophysj.104.049965
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.104.049965v1
88/1/670    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pesen, D.
Right arrow Articles by Hoh, J. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pesen, D.
Right arrow Articles by Hoh, J. H.
Biophysical Journal 88:670-679 (2005)
© 2005 The Biophysical Society

Micromechanical Architecture of the Endothelial Cell Cortex

Devrim Pesen and Jan H. Hoh

Department of Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland

Correspondence: Address reprint requests to Dr. Jan H. Hoh, Dept. of Physiology, Johns Hopkins School of Medicine, 725 N. Wolfe St., Baltimore, MD 21205. Tel.: 410-614-3795; E-mail: jhoh{at}jhmi.edu.

Mechanical properties of living cells are important for cell shape, motility, and cellular responses to biochemical and biophysical signals. Although these properties are predominantly determined by the cytoskeleton, relatively little is known about the mechanical organization of cells at a subcellular level. We have studied the cell cortex of bovine pulmonary artery endothelial cells (BPAECs) using atomic force microscopy (AFM) and confocal fluorescence microscopy (CFM). We show that the contrast in AFM imaging of these cells derives in large part from differences in local mechanical properties, and AFM images of BPAEC reveal the local micromechanical architecture of their apical cortex at ~125 nm resolution. Mechanically the cortex in these cells is organized as a polygonal mesh at two length scales: a coarse mesh with mesh element areas ~0.5–10 µm2, and a finer mesh with areas <0.5 µm2. These meshes appear to be intertwined, which may have interesting implications for the mechanical properties of the cell. Correlated AFM-CFM experiments and pharmacological treatments reveal that actin and vimentin are components of the coarse mesh, but microtubules are not mechanical components of the BPAEC apical cortex.




This article has been cited by other articles:


Home page
Biophys. JHome page
D. Sanchez, N. Johnson, C. Li, P. Novak, J. Rheinlaender, Y. Zhang, U. Anand, P. Anand, J. Gorelik, G. I. Frolenkov, et al.
Noncontact Measurement of the Local Mechanical Properties of Living Cells Using Pressure Applied via a Pipette
Biophys. J., September 15, 2008; 95(6): 3017 - 3027.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
F. T. Arce, J. L. Whitlock, A. A. Birukova, K. G. Birukov, M. F. Arnsdorf, R. Lal, J. G. N. Garcia, and S. M. Dudek
Regulation of the Micromechanical Properties of Pulmonary Endothelium by S1P and Thrombin: Role of Cortactin
Biophys. J., July 15, 2008; 95(2): 886 - 894.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
P. Roca-Cusachs, J. Alcaraz, R. Sunyer, J. Samitier, R. Farre, and D. Navajas
Micropatterning of Single Endothelial Cell Shape Reveals a Tight Coupling between Nuclear Volume in G1 and Proliferation
Biophys. J., June 15, 2008; 94(12): 4984 - 4995.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by the Biophysical Society.