297 A METHOD TO DRIVE CALCIUM SIGNALLING DYNAMICS IN FERTILIZED MOUSE EGGS

Following fertilization, eggs exhibit a series of repetitive increases in intracellular calcium that activate development. The developmental impact of the long-lasting series of Ca 2+ signals is still a subject of controversy. Although several studies using parthenogenetically activated eggs suggest that Ca 2+ dynamics affect post-implantation development, artificial stimulation of Ca 2+ signaling after ICSI in bovine eggs shows that development still remains poor in comparison to fertilized eggs. Such divergence between parthenogenetic studies and those aimed at stimulating ICSI eggs makes it impossible to draw any conclusions regarding the function of Ca 2+ signaling for two reasons. First, non-fertilized eggs do not release Ca 2+ from intracellular stores and their development is compromised due to the absence of paternally-derived chromosomes. Second, because ICSI eggs are excitable, Ca 2+ stimulation generates additional Ca 2+ oscillations that might compromise their development. Moreover, in both cases, Ca 2+ signaling is not physiological. To understand better the function of Ca 2+ signaling at fertilization, we developed a new approach based on micro fluidic technology that makes it possible to drive Ca 2+ signal dynamics of fertilized eggs with no apparent deleterious effects.This method relies on the fact that the properties of the IP3 receptor (IP3R) calcium channel are changed after fertilization, and IP3 and Ca 2+ act as co-agonists to cause Ca 2+ -induced Ca 2+ release (CICR) from intracellular stores. Because Ca 2+ has both an inhibiting and a stimulating function, we exploited these opposing properties. First, we inhibited Ca 2+ release by external washing with Ca 2+ -free medium; this extra cellular washing decreases cytosolic [Ca 2+ ]I, and facilitates dissociation of Ca 2+ ions from the IP3R that in turn decreases the probability of IP3R channel opening. Second, once the IP3R is inhibited, a simple injection of Ca 2+ ions by electropermeabilization triggers channel opening and induces Ca 2+ release. Then, by just varying the time interval and the number of the electrical pulses, it is possible to drive the dynamics of the CICR process that initiates development. Intracellular Ca 2+ imaging demonstrated that fertilized eggs subjected to 24 electrical pulses (1.45kVcm −1 ) every 8min for 3h in the microfluidic processor responded by exhibiting 24 induced-Ca 2+ transients that are caused by calcium release from intracellular stores. All auto-regenerative responses between pulses were inhibited. Among 60 treated embryos transferred to pseudo-pregnant recipients, 40 (67%) developed to term, with birth of live offspring, thus demonstrating that this new methodology does not compromise development. Because the eggs are fertilized, it now becomes possible to study the function of Ca 2+ signaling during egg activation and to evaluate its developmental impact, if any, in association with genomic approaches.