The potentiostatic control of surface charge density and interfacial tensio
n of an electrode immersed in an aqueous electrolyte solution offers a poss
ibility for direct studies of non-specific interactions in cell adhesion. U
nicellular marine alga, Dunaliella tertiolecta (Chlorophyceae) of micromete
r size and flexible cell envelope was used as a model cell and 0.1 M NaCl a
s supporting electrolyte. The dropping mercury electrode acted as in situ a
dhesion sensor and the electrochemical technique of chronoamperometry allow
ed measurement of the spread cell-electrode interface area and the distance
of the closest approach of a cell. The adhesion and spreading of a single
cell at the mercury electrode causes a displacement of counter-ions from th
e electrical double layer over a broad range of the positive and negative s
urface charge densities (from + 16.0 to - 8.2 muC/cm(2)). The flow of compe
nsating current reflects the dynamics of adhesive contact formation and sub
sequent spreading of a cell. The adhesion and spreading rates are enhanced
by the hydrodynamic regime of electrode's growing fluid interface. The dist
ance of the closest approach of an adherent cell is smaller or equal to the
distance of the outer Helmholz plane within the electrical double layer, i
.e. 0.3-0.5 nm. There is a clear evidence of cell rupture for the potential
s of maximum attraction as the area of the contact interface exceeded up to
100 times the cross-section area of a free cell. (C) 2000 Elsevier Science
S.A. All rights reserved.