KYONO, K., HOSHI, K., SAITO, A., TSUIKI, A., HOSHIAI, H. and SUZUKI, M.
Effects of Phospholipase A2, Lysophosphatidyl Choline, and Fatty Acid on the Acrosome Reaction of Human Spermatozoa. Tohoku J. exp. Med., 1984,
144 (3), 257-263 - An in vitro penetration assay employing zona-free hamster eggs was used to study the effects of phospholipase A
2, lysophosphatidyl choline, and fatty acid on the acrosome reaction of human spermatozoa. Human spermatozoa were preincubated for 4hr in modified Biggers, Whitten, and Whittingham's medium (mBWW) containing a specific phospholipase A
2 inhibitor, p-bromophenacyl bromide (p-BPB: 1×10
-5-1×10
-3M), lysophosphatidyl choline (LC: 5-500μg/ml), and arachidonic acid (AA: 5-500μg/ml), prior to the addition of zona-free superovulated hamster eggs. Eggs were examined microscopically 2 or 4hr later for evidence of swelling or decondensing sperm heads in the cytoplasm. Lysophosphatidyl choline increased penetration rates of spermatozoa from 43.2% (control) to 91.4% (LC: 50μg/ml). Arachidonic acid also increased penetration rates from 51.6% (control) to 87.0% (AA: 5μg/ml) and 80.5% (AA: 50μg/ml). p-BPB decreased penetration rates from 90.6% (1% dimethyl sulfoxide) to 16.0°C (1% dimethyl sulfoxide+p-BPB 1×10
-4M). These results suggest that endogenous phospholipase A
2 may break membrane phosphatidyl choline into lysophosphatidyl choline and fatty acid, when the acrosome reaction occurs
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