Reorganization of the flagellum scaffolding induces a sperm standstill during fertilization

Mammalian sperm delve into the female reproductive tract to fertilize the female gamete. The available information about how sperm regulate their motility during the final journey to the fertilization site is extremely limited. In this work, we investigated the structural and functional changes in the sperm flagellum after acrosomal exocytosis (AE) and during the interaction with the eggs. The evidence demonstrates that the double helix actin network surrounding the mitochondrial sheath of the midpiece undergoes structural changes prior to the motility cessation. This structural modification is accompanied by a decrease in diameter of the midpiece and is driven by intracellular calcium changes that occur concomitant with a reorganization of the actin helicoidal cortex. Midpiece contraction occurs in a subset of cells that undergo AE, and live-cell imaging during in vitro fertilization showed that the midpiece contraction is required for motility cessation after fusion is initiated. These findings provide the first evidence of the F-actin network’s role in regulating sperm motility, adapting its function to meet specific cellular requirements during fertilization, and highlighting the broader significance of understanding sperm motility.

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Publication Details

Journal
eLife
Published
2024-11-12
DOI
https://doi.org/10.7554/elife.93792.3
Citations
5
Primary Topic
Reproductive Biology and Fertility
Type
article
Field-Weighted Citation Impact
2.71

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article

Reorganization of the flagellum scaffolding induces a sperm standstill during fertilization

César A. Cárdenas, Alejandro López‐Saavedra, Alberto Darszon, Diego Krapf et al.
5 citations
eLife
Reproductive Biology and Fertility
2.71
article

Reorganization of the flagellum scaffolding induces a sperm standstill during fertilization

César A. Cárdenas, Alejandro López‐Saavedra, Alberto Darszon, Diego Krapf, Gabriel Corkidi, Martina Jabloñski, Mariano G. Buffone, Darío Krapf, Guillermina M. Luque, Adán Guerrero, Xinran Xu, María del Pilar Ramos‐Godínez, Alejandro Linares, Jose L de La Vega Beltran, Víctor Abonza, Aquetzalli Arenas-Hernández, Matias Gomez Elias
article en
5 citations

Abstract

Mammalian sperm delve into the female reproductive tract to fertilize the female gamete. The available information about how sperm regulate their motility during the final journey to the fertilization site is extremely limited. In this work, we investigated the structural and functional changes in the sperm flagellum after acrosomal exocytosis (AE) and during the interaction with the eggs. The evidence demonstrates that the double helix actin network surrounding the mitochondrial sheath of the midpiece undergoes structural changes prior to the motility cessation. This structural modification is accompanied by a decrease in diameter of the midpiece and is driven by intracellular calcium changes that occur concomitant with a reorganization of the actin helicoidal cortex. Midpiece contraction occurs in a subset of cells that undergo AE, and live-cell imaging during in vitro fertilization showed that the midpiece contraction is required for motility cessation after fusion is initiated. These findings provide the first evidence of the F-actin network’s role in regulating sperm motility, adapting its function to meet specific cellular requirements during fertilization, and highlighting the broader significance of understanding sperm motility.

eLifeVol. 13
Consejo Nacional de Investigaciones Científicas y Técnicas (AR), National University of Rosario (AR), Instituto de Biología Molecular y Celular de Rosario (AR), Experimental Medicine and Biology Institute (AR), Universidad Nacional Autónoma de México (MX), Colorado State University (US), Tecnológico de Monterrey (MX)
Chan Zuckerberg Initiative, National Institutes of Health, Agencia Nacional de Promoción Científica y Tecnológica, Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México
Openalex Percentile: Top 9%
Reproductive Biology and Fertility
2.71
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