Journal of Applied Physiology Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 96: 957-966, 2004. First published November 14, 2003; doi:10.1152/japplphysiol.00869.2003
8750-7587/04 $5.00
This Article
Right arrow Full Text Free
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
96/3/957    most recent
00869.2003v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (12)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Norvell, S. M.
Right arrow Articles by Pavalko, F. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Norvell, S. M.
Right arrow Articles by Pavalko, F. M.

Fluid shear stress induction of COX-2 protein and prostaglandin release in cultured MC3T3-E1 osteoblasts does not require intact microfilaments or microtubules

Suzanne M. Norvell,* Suzanne M. Ponik,* Deidre K. Bowen, Rita Gerard, and Fredrick M. Pavalko

Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana 46202

Submitted 15 August 2003 ; accepted in final form 5 November 2003

Cultured osteoblasts express three major types of cytoskeleton: actin microfilaments, microtubules, and intermediate filaments. The cytoskeletal network is thought to play an important role in the transmission and conversion of a mechanical stimulus into a biochemical response. To examine a role for the three different cytoskeletal networks in fluid shear stress-induced signaling in osteoblasts, we individually disrupted actin microfilaments, micro-tubules, and intermediate filaments in MC3T3-E1 osteoblasts with multiple pharmacological agents. We subjected these cells to 90 min of laminar fluid shear stress (10 dyn/cm2) and compared the PGE2 and PGI2 release and induction of cyclooxygenase-2 protein to control cells with intact cytoskeletons. Disruption of actin microfilaments, microtubules, or intermediate filaments in MC3T3-E1 cells did not prevent a significant fluid shear stress-induced release of PGE2 or PGI2. Furthermore, disruption of actin microfilaments or microtubules did not prevent a significant fluid shear stress-induced increase in cyclooxygenase-2 protein levels. Disruption of intermediate filaments with acrylamide did prevent the fluid shear stress-induced increase in cyclooxygenase-2 but also prevented a PGE2-induced increase in cyclooxygenase-2. Thus none of the three major cytoskeletal networks are required for fluid shear stress-induced prostaglandin release. Furthermore, although neither actin microfilaments nor microtubules are required for fluid shear stress-induced increase in cyclooxygenase-2 levels, the role of intermediate filaments in regulation of cyclooxygenase-2 expression is less clear.

osteoblasts; bone; stress-strain; mechanical loading



Address for reprint requests and other correspondence: F. M. Pavalko, Dept. of Cellular and Integrative Physiology, Indiana Univ. School of Medicine, MS 2069, 635 Barnhill Dr., Indianapolis, IN 46202 (E-mail: fpavalko{at}iupui.edu).




This article has been cited by other articles:


Home page
Am. J. Physiol. Cell Physiol.Home page
W. M. Jackson, M. J. Jaasma, R. Y. Tang, and T. M. Keaveny
Mechanical loading by fluid shear is sufficient to alter the cytoskeletal composition of osteoblastic cells
Am J Physiol Cell Physiol, October 1, 2008; 295(4): C1007 - C1015.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
K. Birkenmeier, A. Staudt, W.-H. Schunck, I. Janke, C. Labitzke, T. Prange, C. Trimpert, T. Krieg, M. Landsberger, V. Stangl, et al.
COX-2-dependent and potentially cardioprotective effects of negative inotropic substances released after ischemia
Am J Physiol Heart Circ Physiol, October 1, 2007; 293(4): H2148 - H2154.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. M. D. Malone, N. N. Batra, G. Shivaram, R. Y. Kwon, L. You, C. H. Kim, J. Rodriguez, K. Jair, and C. R. Jacobs
The role of actin cytoskeleton in oscillatory fluid flow-induced signaling in MC3T3-E1 osteoblasts
Am J Physiol Cell Physiol, May 1, 2007; 292(5): C1830 - C1836.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
N. D. Searby, C. R. Steele, and R. K. Globus
Influence of increased mechanical loading by hypergravity on the microtubule cytoskeleton and prostaglandin E2 release in primary osteoblasts
Am J Physiol Cell Physiol, July 1, 2005; 289(1): C148 - C158.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
J. Zaric and C. Ruegg
Integrin-mediated Adhesion and Soluble Ligand Binding Stabilize COX-2 Protein Levels in Endothelial Cells by Inducing Expression and Preventing Degradation
J. Biol. Chem., January 14, 2005; 280(2): 1077 - 1085.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the American Physiological Society.