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(Received for publication, April 21, 1995; and in revised form, June 26, 1995)
A key assumption of most models for calmodulin regulation of smooth
and non-muscle contractility is that calmodulin is freely diffusible at resting
intracellular concentrations of free Ca. However,
fluorescence recovery after photobleaching (FRAP) measurements of three
different fluorescent analogs of calmodulin in cultured bovine tracheal smooth
muscle cells suggest that free calmodulin may be limiting in unstimulated cells.
Thirty-seven % of microinjected calmodulin is immobile by FRAP and the fastest
recovering component has an effective diffusion coefficient 7-fold slower than a
dextran of equivalent size. Combining the FRAP data with extraction data
reported in a previous paper (Tansey, M., Luby-Phelps, K., Kamm, K. E., and
Stull, J. T.(1994) J. Biol. Chem. 269, 9912-9920), we estimate that at
most 5% of total endogenous calmodulin in resting smooth muscle cells is unbound
(freely diffusible). Examination of the Ca
dependence of calmodulin mobility in permeabilized cells reveals that binding
persists even at intracellular Ca
concentrations
as low as 17 nM. When Ca
is elevated to between
450 nM and 3 µM, some of the bound calmodulin is released, as indicated by an
increase in the effective diffusion coefficient and the percent mobile fraction.
At higher Ca
, calmodulin becomes increasingly
immobilized. In about 50% of the cell population, clamping Ca
at micromolar levels results in translocation of cytoplasmic
calmodulin to the nucleus. The compartmentalization and complex dynamics of
calmodulin in living smooth muscle cells have profound implications for
understanding how calmodulin regulates contractility in response to
extracellular signals.
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