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Biophys J, July 2002, p. 172-183, Vol. 83, No. 1
Photon Medical Research Center, Hamamatsu University School of Medicine, Hamamatsu 431-3192, Japan
It has been a long belief that release of substances from
the cell to the extracellular milieu by exocytosis is completed by
diffusion of the substances from secretory vesicles through the fusion
pore. Involvement of any mechanical force that may be superposed on the
diffusion to enhance the releasing process has not been elucidated to
date. We tackled this problem in cultured bovine chromaffin cells using
direct and sensitive methods: the laser-trap forcemetry and the
evanescent-wave fluorescence microscopy. With a laser beam, we trapped
a micro bead in the vicinity of a cell (with 1 µm of separation) and
observed movements of the bead optically. Electrical stimulation of the
cell induced many of rapid and transient movements of the bead in a
direction away from the cell surface. Upon the same stimulation,
secretory vesicles stained with a fluorescent probe, acridine orange,
and excited under the evanescent field illumination, showed a
flash-like response: a transient increase in fluorescence intensity
associated with a diffuse cloud of brightness, followed by a complete
disappearance. These mechanical and fluorescence transients indicate a
directional flow of substances. Blockers of the Cl
channel suppressed the rates of both responses in a characteristic way
but not exocytotic fusion itself. Immunocytochemical studies revealed
the presence of Cl
and K+ channels on the
vesicle membranes. These results suggest that the externalization of
hormones or transmitters upon exocytosis of vesicles is augmented by
secretion of water from the vesicle membrane through the widened fusion
pore, possibly modulating the rate and reach of the hormone or
transmitter release and facilitating transport of the signal molecules
in intercellular spaces.
Biophys J, July 2002, p. 172-183, Vol. 83, No. 1
© 2002 by the Biophysical Society 0006-3495/02/07/172/12 $2.00
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