Role of calcium on the initiation of sperm motility in
the European eel
Luz
Pérez, M. Carmen Vílchez, Víctor Gallego, Marina Morini, David S. Peñaranda,
Juan F. Asturiano
Abstract
Abstract
Sperm from European eel males treated with hCGrec was
washed in a calcium free extender, and sperm motility was activated both in the
presence (seawater, SW) and in the absence of calcium (NaCl+EDTA), and treated
with calcium inhibitors or modulators. The sperm motility parameters were
evaluated by a computer-assisted sperm analysis (CASA) system, and changes in
the [Ca2+]i fluorescence (and in [Na+]i in some cases) were evaluated by flow
cytometry.
After sperm motility was activated in a medium
containing Ca2+ (seawater, SW) the intracellular fluorescence emitted by Ca2+
increased 4-6-fold compared to the levels in quiescent sperm. However, whilst
sperm activation in a Ca-free media (NaCl+EDTA) resulted in a percentage of
motility similar to seawater, the [Ca2+]i levels did not increase at all. This
result strongly suggests that increasing [Ca2+]i is not a pre-requisite for the induction of sperm motility in European
eel sperm. Several sperm velocities (VCL, VSL, VAP) decreased when sperm was
activated in the Ca-free activator, thus supporting the theory that Ca2+ has a
modulatory effect on sperm motility. The results indicate that a calcium/sodium
exchanger (NCX) which is inhibited by bepridil and a calcium calmodulin kinase
(inhibited by W-7), are involved in the sperm motility of the European eel. Our
results indicate that the increase in [Ca2+]i concentrations during sperm
activation is due to an influx from the external medium, but, unlike in most other
species, it does not appear to be necessary for the activation of motility in
European eel sperm.
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