C. Munoz-garay et al., Inwardly rectifying K+ channels in spermatogenic cells: Functional expression and implication in sperm capacitation, DEVELOP BIO, 234(1), 2001, pp. 261-274
To fertilize, mammalian sperm must complete a maturational process called c
apacitation. It is thought that the membrane potential of sperm hyperpolari
zes during capacitation, possibly due to the opening of K+ channels, but el
ectrophysiological evidence is lacking. In this report, using patch-clamp r
ecordings obtained from isolated mouse spermatogenic cells we document the
presence of a novel K+-selective inwardly rectifying current. Macroscopic c
urrent activated at membrane potentials below the equilibrium potential for
K+ and its magnitude was dependent on the external K+ concentration. The c
hannels selected K+ over other monovalent cations, Current was virtually ab
sent when external K+ was replaced with Na+ or N-methyl-D-glucamine. Additi
on of Cs+ or Ba2+ (IC50 of similar to 15 muM) to the external solution effe
ctively blocked K+ current. Dialyzing the cells with a Mg2+-free solution d
id not affect channel activity. Cytosolic acidification reversibly inhibite
d the current. We verified that the resting membrane potential of mouse spe
rm changed from -52 +/- 6 to -66 +/- 9 mV during capacitation in vitro. Not
ably, application of 0.3-1 mM Ba2+ during capacitation prevented this hyper
polarization and decreased the subsequent exocytotic response to zona pellu
cida. A mechanism is proposed whereby opening of inwardly rectifying K+ cha
nnels may produce hyperpolarization under physiological conditions and cont
ribute to the cellular changes that give rise to the capacitated state in m
ature sperm. (C) 2001 Academic Press.