At issue is the type of constitutive equation that can be used to desc
ribe all possible types of deformation of the neutrophil. Here a neutr
ophil undergoing small deformations is studied by aspirating it into a
glass pipet with a diameter that is only slightly smaller than the di
ameter of the spherically shaped cell. After being held in the pipet f
or at least seven seconds, the cell is rapidly expelled and allowed to
recover its undeformed, spherical shape. The recovery takes approxima
tely 15 s. An analysis of the recovery process that treats the cell as
a simple Newtonian liquid drop with a constant cortical (surface) ten
sion gives a value of 3.3 X 10(-5) cm/s for the ratio of the cortical
tension to cytoplasmic viscosity. This value is about twice as large a
s a previously published value obtained with the same model from studi
es of large deformations of neutrophils. This discrepancy indicates th
at the cytoplasmic viscosity decreases as the amount of deformation de
creases. An extrapolated value for the cytoplasmic viscosity at zero d
eformation is approximately 600 poise when a value for the cortical te
nsion of 0.024 dyn/cm is assumed. Clearly the neutrophil does not beha
ve like a simple Newtonian liquid drop in that small deformations are
inherently different from large deformations. More complex models cons
isting either of two or more fluids or multiple shells must be develop
ed. The complex structure inside the neutrophil is shown in scanning e
lectron micrographs of osmotically burst cells and cells whose membran
e has been dissolved away.