J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Vol 458 pp 633-653
Copyright © 1992 by The Physiological Society
This Article
Right arrow Full Text (PDF)
Services
Right arrow Email this article to a friend
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
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Arkett, S A
Right arrow Articles by Sims, S M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arkett, S A
Right arrow Articles by Sims, S M

Substrate influences rat osteoclast morphology and expression of potassium conductances.

S A Arkett, S J Dixon and S M Sims

Department of Physiology, University of Western Ontario, London, Canada.

1. We studied the electrophysiological properties of freshly isolated rat osteoclasts using the whole-cell configuration of the patch-clamp technique. Membrane currents were recorded from cells plated on three substates: dentine, type I collagen and glass. 2. Based on their morphology, we defined two categories of osteoclasts. 'Rounded' osteoclasts were dome-shaped and lacked lamellipodia. 'Spread' osteoclasts were flattened and had lamellipodia. The proportion of 'rounded' osteoclasts was significantly greater when cells were plated on dentine or type I collagen than when cells were plated on glass. 3. 'Spread' osteoclasts expressed an inwardly rectifying K+ conductance regardless of the substrate on which they were plated. 4. 'Rounded' osteoclasts, on all substrates, expressed a transient, outwardly rectifying conductance that was selective for K+ based on: reversal of deactivation tail currents at -74 mV; a 60 mV shift in tail current reversal potential for 10-fold change in [K+]o; and blockade of outward current by extracellular 4-aminopyridine, charybdotoxin, and intracellular Cs+. The outward K+ current had an activation threshold of approximately -50 mV, with half-activation at -29 mV. The current also exhibited voltage-dependent inactivation, with half-inactivation at approximately -40 mV. 5. Outward K+ current in 'rounded' osteoclasts was reduced when extracellular Ca2+ was removed and upon addition of Ni2+, but was unaffected by Cd2+ or nifedipine. 6. 'Rounded' osteoclasts had large whole-cell capacitance for their apparent surface area. Capacitance was positively correlated with K+ conductance. The additional surface membrane we detected through capacitance measurements may be the 'ruffled border' of actively resorbing osteoclasts. 7. We conclude that substrate influences the expression of osteoclast phenotype, as defined by morphology and K+ conductances. 'Rounded' osteoclasts express an outwardly rectifying K+ conductance, with no apparent inwardly rectifying K+ conductance. In contrast, 'spread' osteoclasts exhibit an inwardly rectifying K+ conductance with no outwardly rectifying K+ conductance. The 'spread' phenotype may represent a motile phase, while the 'rounded' phenotype may represent a resorptive phase of osteoclastic activity.




This article has been cited by other articles:


Home page
EndocrinologyHome page
J.-P. Li, H. Kajiya, F. Okamoto, A. Nakao, T. Iwamoto, and K. Okabe
Three Na+/Ca2+ Exchanger (NCX) Variants Are Expressed in Mouse Osteoclasts and Mediate Calcium Transport during Bone Resorption
Endocrinology, May 1, 2007; 148(5): 2116 - 2125.
[Abstract] [Full Text] [PDF]


Home page
J. Dent. Res.Home page
P. Valverde, T. Kawai, and M.A. Taubman
Potassium Channel-blockers as Therapeutic Agents to Interfere with Bone Resorption of Periodontal Disease
J. Dent. Res., June 1, 2005; 84(6): 488 - 499.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
H. Kajiya, F. Okamoto, H. Fukushima, K. Takada, and K. Okabe
Mechanism and role of high-potassium-induced reduction of intracellular Ca2+ concentration in rat osteoclasts
Am J Physiol Cell Physiol, August 1, 2003; 285(2): C457 - C466.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
A. F. Weidema, S. J. Dixon, and S. M. Sims
Activation of P2Y but not P2X4 nucleotide receptors causes elevation of [Ca2+]i in mammalian osteoclasts
Am J Physiol Cell Physiol, June 1, 2001; 280(6): C1531 - C1539.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
R. L. Lees and J. N. M. Heersche
Differences in regulation of pHi in large (>= 10 nuclei) and small (<= 5 nuclei) osteoclasts
Am J Physiol Cell Physiol, September 1, 2000; 279(3): C751 - C761.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Nordstrom, L. D. Shrode, O. D. Rotstein, R. Romanek, T. Goto, J. N.M. Heersche, M. F. Manolson, G. F. Brisseau, and S. Grinstein
Chronic Extracellular Acidosis Induces Plasmalemmal Vacuolar Type H+ ATPase Activity in Osteoclasts
J. Biol. Chem., March 7, 1997; 272(10): 6354 - 6360.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Nordström, O. D. Rotstein, R. Romanek, S. Asotra, J. N. M. Heersche, M. F. Manolson, G. F. Brisseau, and S. Grinstein
Regulation of Cytoplasmic pH in Osteoclasts
J. Biol. Chem., February 3, 1995; 270(5): 2203 - 2212.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 The Physiological Society.