In vitro aged rabbit erythrocytes are 2- to 3-fold less sensitive than
fresh erythrocytes to lysis by the alpha toxin of Staphylococcus aure
us. Previously, we correlated the loss in hemolytic sensitivity as cel
ls aged with the proteolytic degradation of Band 3, a putative binding
site for staphylococcal alpha toxin. Here we separated young and old
erythrocytes by density gradient centrifugation and compared their pat
terns of lysis by alpha toxin. Derivative plots of lytic-time curves e
xhibited two lytic peaks for young erythrocytes versus a single peak f
or the aged erythrocytes. Hit analysis showed that the first peak in t
he young cells was generated by the monomeric form of the toxin while
the second peak involved the polymeric form. Similar analysis of the s
ingle peak in the aged erythrocytes showed that only a monomeric form
of the toxin is involved in the lysis. Furthermore, analysis of alpha
toxin receptor (Band 3) indicated that the receptor is gradually lost
as erythrocytes age. This loss in Band 3 is proportional to the decrea
se in the rate of lysis by alpha toxin. Based on these comparisons we
suggest that the intact Band 3 promotes polymeric assembly of the alph
a toxin which becomes disrupted by the age-related changes occurring i
n the receptor.