Intracellular calcium-dependent regulation of the sperm-specific calcium-activated potassium channel, hSlo3, by the BK(Ca) activator LDD175.
10.4196/kjpp.2017.21.2.241
- Author:
Tharaka Darshana WIJERATHNE
1
;
Jihyun KIM
;
Dongki YANG
;
Kyu Pil LEE
Author Information
1. Laboratory of Physiology, College of Veterinary Medicine, Chungnam National University, Daejeon 34134, Korea. kplee@cnu.ac.kr
- Publication Type:Original Article
- Keywords:
Ca²⁺-activated potassium channel;
hLRRC52;
hSlo3;
KSper;
LDD175;
Sperm motility
- MeSH:
4-Aminopyridine;
Animals;
Cell Membrane;
Fertilization;
HEK293 Cells;
Humans;
Hydrogen-Ion Concentration;
Membrane Potentials;
Membranes;
Mice;
Potassium Channels, Calcium-Activated*;
Sperm Capacitation;
Sperm Motility;
Spermatozoa;
Tea
- From:The Korean Journal of Physiology and Pharmacology
2017;21(2):241-249
- CountryRepublic of Korea
- Language:English
-
Abstract:
Plasma membrane hyperpolarization associated with activation of Ca²⁺-activated K⁺ channels plays an important role in sperm capacitation during fertilization. Although Slo3 (slowpoke homologue 3), together with the auxiliary γ2-subunit, LRRC52 (leucine-rich-repeat–containing 52), is known to mediate the pH-sensitive, sperm-specific K⁺ current KSper in mice, the molecular identity of this channel in human sperm remains controversial. In this study, we tested the classical BK(Ca) activators, NS1619 and LDD175, on human Slo3, heterologously expressed in HEK293 cells together with its functional interacting γ2 subunit, hLRRC52. As previously reported, Slo3 K⁺ current was unaffected by iberiotoxin or 4-aminopyridine, but was inhibited by ~50% by 20 mM TEA. Extracellular alkalinization potentiated hSlo3 K⁺ current, and internal alkalinization and Ca²⁺ elevation induced a leftward shift its activation voltage. NS1619, which acts intracellularly to modulate hSlo1 gating, attenuated hSlo3 K⁺ currents, whereas LDD175 increased this current and induced membrane potential hyperpolarization. LDD175-induced potentiation was not associated with a change in the half-activation voltage at different intracellular pHs (pH 7.3 and pH 8.0) in the absence of intracellular Ca²⁺. In contrast, elevation of intracellular Ca²⁺ dramatically enhanced the LDD175-induced leftward shift in the half-activation potential of hSlo3. Therefore, the mechanism of action does not involve pH-dependent modulation of hSlo3 gating; instead, LDD175 may modulate Ca²⁺-dependent activation of hSlo3. Thus, LDD175 potentially activates native KSper and may induce membrane hyperpolarization-associated hyperactivation in human sperm.
