Sphingolipids as key mediators in folliculogenesis and female fertility

This review investigates the regulatory functions of sphingolipids-particularly sphingosine-1-phosphate (S1P) and ceramide-in the process of ovarian folliculogenesis. It emphasizes how the dynamic balance between ceramide and S1P, orchestrated by enzymes like sphingomyelinase, ceramidase, and sphingosine kinase (SphK1/2), governs follicle development, survival, and reproductive potential.

A comprehensive review of recent experimental and clinical studies was performed to examine the impact of sphingolipids and their metabolic enzymes on follicular activation, growth, and maturation. Special focus was placed on the signaling mechanisms mediated by S1P and ceramide in ovarian cells.

Sphingolipids are essential mediators of proliferation, differentiation, and programmed cell death during folliculogenesis. S1P enhances follicle survival and growth by activating S1P receptors (notably S1PR1 and S1PR3), which in turn stimulate PI3K/Akt/mTOR and ERK/MAPK signaling cascades. Additionally, S1P-induced calcium mobilization via Gq- and Gi-coupled pathways supports metabolic resilience and cellular longevity. Acting as a pro-survival factor, S1P is particularly influential during physiological events such as the LH surge. Conversely, ceramide-whether derived from sphingomyelin hydrolysis or de novo synthesis-accumulates in mitochondria and promotes apoptosis by activating Bax and suppressing Bcl-2 family proteins. The interplay between ceramide and S1P, often referred to as the "sphingolipid rheostat," plays a central role in determining follicular destiny.

Modulating sphingolipid signaling and its enzymatic regulators holds promise as a therapeutic avenue for enhancing ovarian function and treating gynecological conditions. This review highlights the critical importance of maintaining a functional ceramide/S1P balance to preserve follicular viability and overall reproductive health.