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The sodium-proton exchangers sNHE and NHE1 control plasma membrane hyperpolarization in mouse sperm.

Analia G Novero | Paulina Torres Rodríguez | José L De la Vega Beltrán | Liz J Schiavi-Ehrenhaus | Guillermina M Luque | Micaela Carruba | Cintia Stival | Iñaki Gentile | Carla Ritagliati | Celia M Santi | Takuya Nishigaki | Diego Krapf | Mariano G Buffone | Alberto Darszon | Claudia L Treviño | Dario Krapf
bioRxiv : the preprint server for biology | 2024

Sperm capacitation, crucial for fertilization, occurs in the female reproductive tract and can be replicated in vitro using a medium rich in bicarbonate, calcium, and albumin. These components trigger the cAMP-PKA signaling cascade, proposed to promote hyperpolarization of the mouse sperm plasma membrane through activation of SLO3 K+ channel. Hyperpolarization is a hallmark of capacitation: proper membrane hyperpolarization renders higher in vitro fertilizing ability, while Slo3 KO mice are infertile. However, the precise regulation of SLO3 opening remains elusive. Our study challenges the involvement of PKA in this event and reveals the role of Na+/H+ exchangers. During capacitation, calcium increase through CatSper channels activates NHE1, while cAMP directly stimulates the sperm-specific NHE, collectively promoting the alkalinization threshold needed for SLO3 opening. Hyperpolarization then feeds back Na+/H+ activity. Our work is supported by pharmacology, and a plethora of KO mouse models, and proposes a novel pathway leading to hyperpolarization.

Pubmed ID: 38496535

Research resources used in this publication

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Associated grants

  • Agency: NICHD NIH HHS, United States
    Id: R01 HD038082
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD069631
  • Agency: NICHD NIH HHS, United States
    Id: R01 HD106968

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