We hypothesized that the requirement for Ca2+-dependent exocytosis in tell-
membrane repair is to provide an adequate lowering of membrane tension to p
ermit membrane resealing. We used laser tweezers to form membrane tethers a
nd measured the force of those tethers to estimate the membrane tension of
Swiss 3T3 fibroblasts after membrane disruption and during resealing. These
measurements show that, for fibroblasts wounded in normal Ca2+ Ringer's so
lution, the membrane tension decreased dramatically after the wounding and
resealing coincided with a decrease of similar to 60% of control tether for
ce values. However, the tension did not decrease if cells were wounded in a
low Ca2+ Ringer's solution that inhibited both membrane resealing and exoc
ytosis. When cells were wounded twice in normal Ca2+ Ringer's solution, dec
eases in tension at the second wound were 2.3 times faster than at the firs
t wound, correlating well with twofold faster resealing rates for repeated
wounds. The facilitated resealing to a second wound requires a new vesicle
pool, which is generated via a protein kinase C (PKC)-dependent and brefeld
in A (BFA)-sensitive process. Tension decrease at the second wound was slow
ed or inhibited by PKC inhibitor or BFA. Lowering membrane tension by cytoc
halasin D treatment could substitute for exocytosis and could restore membr
ane resealing in low Ca2+ Ringer's solution.