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(Received for publication, October 12, 1994; and in revised form, January 9,
1995) From the
Fertilization of mature mouse oocytes triggered highly
repetitive Ca Preincubation of oocytes with
thapsigargin or ryanodine significantly attenuated the normal
fertilization Ca
Volume 270,
Number 12,
Issue of March 24, 1995 pp. 6671-6677
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Release
Increase during Meiotic Maturation of Mouse Oocytes (*)
oscillations lasting 2-3 h.
However, immature oocytes generated only two or three oscillations,
which ceased within 1 h. Development of repetitive Ca
transients to sperm occurred late in oocyte maturation and was
dependent on cytoplasmic modifications that were independent of cell
cycle progression from metaphase I to metaphase II. Immature oocytes
released significantly less Ca
from stores than
mature oocytes in response to ionomycin and thapsigargin. Ryanodine had
no effect on intracellular Ca
in maturing oocytes but
stimulated an increase in Ca
in mature oocytes. The
ability of ryanodine to increase Ca
levels was,
however, strain-dependent.
response, causing a decrease in the
number and the rate of rise of the transients. The inhibition of
sperm-induced Ca
transients by ryanodine was
independent of its ability to cause an immediate Ca
increase. Low concentrations of ryanodine had no effect on
resting Ca
levels but inhibited Ca
oscillations at fertilization. Similarly Ca
oscillations were blocked in oocytes from a strain of mouse that
showed no immediate Ca
increase with ryanodine. These
results suggest that modifications in Ca
stores and
ryanodine-sensitive Ca
release mechanisms during
oocyte maturation play an important role in Ca
oscillations at fertilization.
)
,
inositol trisphosphate; CICR, Ca
-induced
Ca
release; GV, germinal vesicle; GVBD, GV breakdown;
BSA, bovine serum albumin.
We thank Dr. Karl Swann for critical reading of this
manuscript.
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
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