4.4 Article

Patterns of [Ca2+]i mobilization and cell response in human spermatozoa exposed to progesterone

Journal

DEVELOPMENTAL BIOLOGY
Volume 302, Issue 1, Pages 324-332

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2006.09.040

Keywords

sperm; progesterone; calcium; calcium store; secretory pathway calcium ATPase

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Human spermatozoa stimulated with progesterone (a product of the cumulus and thus encountered by sperm prior to fertilization in vivo) apparently mobilize Ca2+ and respond very differently according to the way in which the steroid is presented. A progesterone concentration ramp (0-3 mu M) induces [Ca2+](i) oscillations (repetitive store mobilization) which modify flagellar beating, whereas bolus application of micromolar progesterone causes a single large transient (causing acrosome reaction) which is apparently dependent upon Ca2+ influx. We have investigated Ca2+-mobilization and functional responses in human sperm exposed to 3 mu M progesterone. The [Ca2+](i) response to progesterone was abolished by 4 min incubation in 0 Ca2+ medium (2 mM EGTA) but in nominally Ca2+-free medium (no added Ca2+; 0 EGTA) a smaller, slow response occurred. Single cell imaging showed a similar effect of nominally Ca2+-free medium and approximate to 5% of cells generated a small transient even in the presence of EGTA. When cells were exposed to EGTA-containing saline (5 min) and then returned to nominally Ca2+-free medium before stimulation, the [Ca2+](i) transient was greatly delayed (approximate to 50 s) and rise time was doubled in comparison to cells not subjected to EGTA pretreatment. We conclude that mobilization of stored Ca2+ contributes a 'slow' component to the progesterone-induced [Ca2+](i) transient and that incubation in EGTA-buffered saline is able rapidly to deplete this store. Analysis of flagellar activity induced by 3 mu M progesterone showed an effect (modified beating) associated with the [Ca2+](i) transient, in > 80% of cells bathed in nominally Ca2+-free medium. This was reduced greatly in cells subjected to 5 min EGTA pre-treatment. The store-mediated transient showed a pharmacological sensitivity similar to that of progesterone-induced [Ca2+](i) oscillations (consistent with filling of the store by an SPCA) suggesting that the transient induced by micromolar progesterone is a 'single shot' activation of the same store that generates Ca2+ oscillations. (c) 2006 Elsevier Inc. All rights reserved.

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