ACTIVE CALCIUM MOBILIZATION FROM A THAPSIGARGIN-SENSITIVE POOL BY FREE 32:5n-6 IN SPERMATIDS

SANTIAGO VALTIERRA, F.X.; PEÑALVA, D.A.; LUQUEZ, J.M.; AVELDAÑO, M.I.; REYES, J.G.; ORESTI, G.M.

Congreso; LVI Reunión Anual de la Sociedad Argentina de Bioquímica y Biología molecular; 2020

In their free form, long chain (C18-22) polyunsaturated fatty acids (PUFA), especially 20:4n-6, can modify calcium homeostasis in male germ cells. These cells also contain unusual n-6 very-long-chain (VLC) PUFA (28:4, 30:5, and 32:5), in non-hydroxy (n-V) and 2-hydroxy (h-V) forms, in their membrane sphingolipids. Potential biological roles of VLCPUFA, as free fatty acids (FFA), in the physiology of male germ cells are unknown. In this study we explored the ability of n-V FFA, and their h-V counterparts, to modify the intracellular calcium homeostasis in rat spermatids. After obtaining the n-V and h-V FFA from testicular sphingomyelin, their natural source, each group was separately added to spermatids suspensions at an 8 µM concentration. The n-V FFA increased the intracellular calcium concentration ([Ca2+]i) in spermatids several fold more intensely than did the h-V FFA. After isolating the components of n-V and h-V mixtures by HPLC to study the effect of each VLCPUFA, free n-32:5 was found to be the most active in increasing the [Ca2+]i, followed by n-30:5, while h-32:5 augmented it only slightly. In addition to fatty acid-specific, the response was dose-dependent. The rates of [Ca2+]i upsurge were independent of the presence of extracellular calcium. Pretreatment with thapsigargin inhibited the effect of n-32:5, suggesting that this FFA promotes the release of Ca2+ from intracellular calcium stores, mainly the endoplasmic reticulum. The n-V FFA did not seem to exert their effects through the G protein-coupled receptor GPR120, a putative receptor for free PUFA, as they occurred in the presence of a GPR120 inhibitor. Ceramides containing the same fatty acids did not modify [Ca2+]i, thus the observed [Ca2+]i increases may be attributed to the FFA themselves. The possibility that they occur after VLC-FFAs are converted into other bioactive compounds remains to be investigated. Our results revealed a biological activity of VLCPUFA that suggests a physiological role for these fatty acids. As VLCPUFA-mediated Ca2+ rises occurred in spermatids, they may activate Ca2+ signaling pathways with specific functional targets in germ cells differentiation.