Multinucleated osteoclasts from rabbit long bone, 1-6 days in culture,
respond to mechanical perturbation with a transient increase of intra
cellular calcium concentration ([Ca2+](i)), as measured with the fluor
escent indicator fluo-3 on a confocal laser scanning microscope. In ex
periments with different extracellular calcium concentrations (from 11
.8 mM to calcium-free), the incidence, the magnitude, and the duration
of [Ca2+](i) responses decreases with decreasing bathing [Ca2+]. Foll
owing mechanical perturbation, a thapsigargin-induced [Ca2+](i) respon
se has a lower magnitude than the thapsigargin-induced response withou
t mechanical perturbation. In thapsigargin-pretreated osteoclasts the
mechanical perturbation-induced rise in [Ca2+](i) is larger and longer
than in control cells. Ni2+ inhibits the incidence and decreases both
the magnitude and the duration of the responses, while nifedipine, ve
rapamil, and Gd3+ have no effect. These measurements show that rabbit
osteoclasts transduce a mechanical perturbation of the cell membrane i
nto a [Ca2+](i) signal via both a calcium influx and an internal calci
um release. (C) 1995 Wiley-Liss, Inc.