Chemotaxis, the directional locomotion of a cell toward a source of a
chemical gradient, is an important phenomenon occurring for mobilizing
immune cells at sites-of infection and injury. This phenomenon has be
en modelized in analyzing the movement in vitro of a chemoattracted ce
ll inside a glass micropipette. A microneedle filled with fMLP, N-form
yl-methionyl-leucyl-phenylalanine, at a concentration of 9.10(-7) M in
1% gelatin, is inserted in a glass micropipette containing Hanks buff
er solution. After diffusion of fMLP in the glass micropipette until a
constant gradient is established, the tip of the glass micropipette i
s moved near a polymorphonuclear neutrophil. Its spontaneous movement
inside the micropipette towards the chemotactic source can be observed
and quantified. Without any counter-pressure (positive pressure), the
cell spontaneously advances with an average velocity of 0.14 +/- 0.04
mu m/s. Corresponding to the maxi mal strength developed by the cell
during its motion, the required strength to stop the chemotactic migra
tion has been estimated to be 39 +/- 4 nN.Giving both qualitative and
quantitative information on the dynamics of cell motility, this experi
ment will be helpful in the understanding of some aspects of cell moti
lity in the tissues