The Cell Biology of Fertilization

A special issue of Cells (ISSN 2073-4409). This special issue belongs to the section "Cell Proliferation and Division".

Deadline for manuscript submissions: closed (31 March 2024) | Viewed by 1457

Special Issue Editors


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Guest Editor
Research Director, Stazione Zoologica Anton Dohrn, Napoli, Italy
Interests: maturation; fertilization, actin cytoskeleton, calcium signalling; cell biology; developmental biology

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Guest Editor
Research Infrastructures for Marine Biological Resources, Napoli, Italy
Interests: maturation; fertilization, actin cytoskeleton, calcium signalling; cell biology; developmental biology

Special Issue Information

Dear Colleagues,

Fertilization that is required for activating oocytes stimulated at different maturation stages is a critical process in embryo development. Since the beginning, the study of oogenesis and spermatogenesis and the many events that precede and follow the interaction of male and female gametes have highlighted the complexity of the fertilization process. During the past few years, significant advances have been made in deciphering the crucial role played by the structural reorganization of the cortex of oocytes during the maturation of several species that are necessary to ensure optimal fertilization conditions. Studies on the sequential spatial/temporal series of fast events regulating the fertilization process have provided live cell imaging methodologies and insights for clarifying the changes induced by the egg's extracellular coats on the sperm physiology and the interaction of species–species complementary receptors on the sperm and egg plasma membranes. Following gamete fusion, the changes in the egg plasma membrane potential, intracellular calcium and pH, and the subsequent actin remodeling to ensure monospermic fertilization and regulate cleavage demonstrate the complex program of cell signaling in sustaining the control of vital cellular activities. Thus, in addition to shedding light on the cell signaling between male and female gametes, studies on maturation and fertilization processes using large cells will help us understand the basic structural and biochemical mechanisms regulating critical cellular functions in response to a myriad of stimuli.

This Special Issue aims to assemble various lines of research to provide an in-depth description of the "state-of-the-art" regarding the fertilizability of gametes, their species-specific interaction, the signal transduction of egg activation, and cleavage.

Dr. Luigia Santella
Dr. Nunzia Limatola
Guest Editors

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Keywords

  • oocyte maturation
  • acrosome reaction
  • gamete interaction
  • actin remodelling
  • calcium
  • monospermy

Published Papers (1 paper)

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Review

12 pages, 1276 KiB  
Review
Sperm-Induced Ca2+ Release in Mammalian Eggs: The Roles of PLCζ, InsP3, and ATP
by Karl Swann
Cells 2023, 12(24), 2809; https://0-doi-org.brum.beds.ac.uk/10.3390/cells12242809 - 10 Dec 2023
Viewed by 983
Abstract
Mammalian egg activation at fertilization is triggered by a long-lasting series of increases in cytosolic Ca2+ concentration. These Ca2+ oscillations are due to the production of InsP3 within the egg and the subsequent release of Ca2+ from the endoplasmic [...] Read more.
Mammalian egg activation at fertilization is triggered by a long-lasting series of increases in cytosolic Ca2+ concentration. These Ca2+ oscillations are due to the production of InsP3 within the egg and the subsequent release of Ca2+ from the endoplasmic reticulum into the cytosol. The generation of InsP3 is initiated by the diffusion of sperm-specific phospholipase Czeta1 (PLCζ) into the egg after gamete fusion. PLCζ enables a positive feedback loop of InsP3 production and Ca2+ release which then stimulates further InsP3 production. Most cytosolic Ca2+ increases in eggs at fertilization involve a fast Ca2+ wave; however, due to the limited diffusion of InsP3, this means that InsP3 must be generated from an intracellular source rather than at the plasma membrane. All mammalian eggs studied generated Ca2+ oscillations in response to PLCζ, but the sensitivity of eggs to PLCζ and to some other stimuli varies between species. This is illustrated by the finding that incubation in Sr2+ medium stimulates Ca2+ oscillations in mouse and rat eggs but not eggs from other mammalian species. This difference appears to be due to the sensitivity of the type 1 InsP3 receptor (IP3R1). I suggest that ATP production from mitochondria modulates the sensitivity of the IP3R1 in a manner that could account for the differential sensitivity of eggs to stimuli that generate Ca2+ oscillations. Full article
(This article belongs to the Special Issue The Cell Biology of Fertilization)
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