2025 AMA Research Challenge – Member Premier Access

October 22, 2025

Virtual only, United States

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Abstract Title Platelet-activating factor has a positive effect on intracellular calcium and motility in sea urchin spermatozoa Background Platelet-activating factor (PAF) is a pleiotropic phospholipid molecule first described for its role in inflammation, vasodilation, and platelet aggregation. PAF is also known to regulate many different reproductive processes, such as fertilization. Studies have suggested PAF as an autocrine mediator of fertilization via induction of spermatozoa capacitation, a calcium mediated event involving hyperactivation of motility, making it of emergent interest in fundamental reproductive research with fertility applications. While PAF is produced by sea urchin spermatozoa, the mechanism of action of PAF in this organism is uncertain. Therefore, the objective of this study was to determine the effect of exogenous PAF on intracellular calcium and spermatozoa motility in the sea urchin, a time-honored model for developmental physiology studies. Methods Spermatozoa shedding from Lytechinus variegatus sea urchins was induced by peri-oral injection of 0.5M KCl. Sperm motility, before and after PAF (10-7 M) exposure, was assessed via a computer-assisted semen analyzer (SQA-V Gold, Medical Electronic Systems). Spermatozoa were tagged with a calcium indicator (5µM Fluo-4), incubated for 1 hour at room temperature, and then centrifuged (1,000xg; 1 minute) to remove excess Fluo-4. To minimize movement, spermatozoa were imaged on poly-L-lysine coated slides. Calcium release was observed before and after PAF (10-7 M) exposure via fluorescence imaging acquired using an epifluorescence microscope (Revolve Echo) with a FITC filter set. Images were analyzed using a custom Python-based workflow with Fluo-4 signal intensity recorded as relative fluorescence units (RFU). Lyso-PAF, the biologically inactive form of PAF, was used as a control. Data were analyzed via paired t-test (Sigma Plot). Results There was a significant (p<0.05) rise in spermatozoa motility following the addition of PAF (mean SMI=71) over control (mean SMI=47). There was also a significant difference (p<0.05) in intracellular calcium levels following PAF administration (control 14.57 RFU; PAF 17.77 RFU). Lyso-PAF had no effect on motility or intracellular calcium levels. Conclusion This study validates PAF as a positive mediator of spermatozoa motility, most likely via an increase in intracellular calcium. Insight into a potential mechanism by which PAF exerts its effects via intracellular calcium release may lead to identification of cell-surface PAF receptors coupled to Gq protein alpha subunits on spermatozoa of the sea urchin. Additional studies are warranted to further understand the cause-and-effect relationship between PAF and intracellular calcium on spermatozoa motility.

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