TY - JOUR
T1 - TRPV4 is the temperature-sensitive ion channel of human sperm
AU - Mundt, Nadine
AU - Spehr, Marc
AU - Lishko, Polina V.
N1 - Publisher Copyright:
© Mundt et al.
PY - 2018/7/2
Y1 - 2018/7/2
N2 - Ion channels control the ability of human sperm to fertilize the egg by triggering hyperactivated motility, which is regulated by membrane potential, intracellular pH, and cytosolic calcium. Previous studies unraveled three essential ion channels that regulate these parameters: (1) the Ca 2+ channel CatSper, (2) the K + channel KSper, and (3) the H + channel Hv1. However, the molecular identity of the sperm Na + conductance that mediates initial membrane depolarization and, thus, triggers downstream signaling events is yet to be defined. Here, we functionally characterize DSper, the Depolarizing Channel of Sperm, as the temperature-activated channel TRPV4. It is functionally expressed at both mRNA and protein levels, while other temperature-sensitive TRPV channels are not functional in human sperm. DSper currents are activated by warm temperatures and mediate cation conductance, that shares a pharmacological profile reminiscent of TRPV4. Together, these results suggest that TRPV4 activation triggers initial membrane depolarization, facilitating both CatSper and Hv1 gating and, consequently, sperm hyperactivation.
AB - Ion channels control the ability of human sperm to fertilize the egg by triggering hyperactivated motility, which is regulated by membrane potential, intracellular pH, and cytosolic calcium. Previous studies unraveled three essential ion channels that regulate these parameters: (1) the Ca 2+ channel CatSper, (2) the K + channel KSper, and (3) the H + channel Hv1. However, the molecular identity of the sperm Na + conductance that mediates initial membrane depolarization and, thus, triggers downstream signaling events is yet to be defined. Here, we functionally characterize DSper, the Depolarizing Channel of Sperm, as the temperature-activated channel TRPV4. It is functionally expressed at both mRNA and protein levels, while other temperature-sensitive TRPV channels are not functional in human sperm. DSper currents are activated by warm temperatures and mediate cation conductance, that shares a pharmacological profile reminiscent of TRPV4. Together, these results suggest that TRPV4 activation triggers initial membrane depolarization, facilitating both CatSper and Hv1 gating and, consequently, sperm hyperactivation.
UR - http://www.scopus.com/inward/record.url?scp=85052205665&partnerID=8YFLogxK
U2 - 10.7554/eLife.35853
DO - 10.7554/eLife.35853
M3 - Article
C2 - 29963982
AN - SCOPUS:85052205665
SN - 2050-084X
VL - 7
JO - eLife
JF - eLife
M1 - e35853
ER -