133 research outputs found

    Mechanical Property Characterization of Mouse Zona Pellucida

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    Previous intracytoplasmic sperm injection (ICSI) studies have indicated significant variation in ICSI success rates among different species. In mouse ICSI, the zona pellucida (ZP) undergoes a hardening process at fertilization in order to prevent subsequent sperm from penetrating. There have been few studies investigating changes in the mechanical properties of mouse ZP post fertilization. To characterize mouse ZP mechanical properties and quantitate the mechanical property differences of the ZP before and after fertilization, a microelectromechanical systems-based multiaxis cellular force sensor has been developed. A microrobotic cell manipulation system employing the multiaxis cellular force sensor is used to conduct mouse ZP force sensing, establishing a quantitative relationship between applied forces and biomembrane structural deformations on both mouse oocytes and embryos. An analytical biomembrane elastic model is constructed to describe biomembrane mechanical properties. The characterized elastic modulus of embryos is 2.3 times that of oocytes, and the measured forces for puncturing embryo ZP are 1.7 times those for oocyte ZP. The technique and model presented in this paper can be applied to investigations into the mechanical properties of other biomembranes, such as the plasma membrane of oocytes or other cell types

    Reversible Disassembly of the Actin Cytoskeleton Improves the Survival Rate and Developmental Competence of Cryopreserved Mouse Oocytes

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    Effective cryopreservation of oocytes is critically needed in many areas of human reproductive medicine and basic science, such as stem cell research. Currently, oocyte cryopreservation has a low success rate. The goal of this study was to understand the mechanisms associated with oocyte cryopreservation through biophysical means using a mouse model. Specifically, we experimentally investigated the biomechanical properties of the ooplasm prior and after cryopreservation as well as the consequences of reversible dismantling of the F-actin network in mouse oocytes prior to freezing. The study was complemented with the evaluation of post-thaw developmental competence of oocytes after in vitro fertilization. Our results show that the freezing-thawing process markedly alters the physiological viscoelastic properties of the actin cytoskeleton. The reversible depolymerization of the F-actin network prior to freezing preserves normal ooplasm viscoelastic properties, results in high post-thaw survival and significantly improves developmental competence. These findings provide new information on the biophysical characteristics of mammalian oocytes, identify a pathophysiological mechanism underlying cryodamage and suggest a novel cryopreservation method

    Mammalian Sperm Motility: Observation and Theory

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    Mammalian spermatozoa motility is a subject of growing importance because of rising human infertility and the possibility of improving animal breeding. We highlight opportunities for fluid and continuum dynamics to provide novel insights concerning the mechanics of these specialized cells, especially during their remarkable journey to the egg. The biological structure of the motile sperm appendage, the flagellum, is described and placed in the context of the mechanics underlying the migration of mammalian sperm through the numerous environments of the female reproductive tract. This process demands certain specific changes to flagellar movement and motility for which further mechanical insight would be valuable, although this requires improved modeling capabilities, particularly to increase our understanding of sperm progression in vivo. We summarize current theoretical studies, highlighting the synergistic combination of imaging and theory in exploring sperm motility, and discuss the challenges for future observational and theoretical studies in understanding the underlying mechanics.\ud Acronyms and Definitions\ud Acrosome: the cap of the sperm head containing enzymes allowing penetration of the zona pellucida via the acrosome reaction\ud Adenosine triphosphate (ATP): the currency unit of chemical energy transfer in living cells\ud Axoneme: a phylogenetically conserved structure within the eukaryotic flagellum consisting of a ring of nine microtubule doublets and a central pair, frequently referred to as 9 + 2\ud Bending moment density: the moment per unit length associated with flagellar bending; it can be divided into a hydrodynamic moment, an elastic moment (from the flagellar bending stiffness), an active moment (generated by dyneins exerting forces between adjacent microtubule doublets), and a passive moment resisting shear\ud Capacitation: the physiological state of a sperm required for fertilization, which is accompanied by the motility patterns associated with hyperactivation, characterized in saline by high-amplitude asymmetric beating\ud Central pair: a pair of microtubules along the length of the axoneme, symmetrically and slightly offset from the axoneme centerline\ud Cumulus oophorus: the outer vestment of the mammalian egg consisting of hundreds of cells radiating out from the egg embedded within a non-Newtonian hyaluronic acid gel\ud Dynein: a molecular motor within the axoneme, attached between adjacent microtubule doublets, that exerts a shearing force to induce axonemal bending\ud Flagellum: a motile cellular appendage that drives the swimming of sperm and other cells; this article focuses on the eukaryotic flagellum\ud Microtubule doublet: a pair of proteinaceous filament structures running the length of the axoneme; dyneins drive their bending, which induces flagellar motion\ud Mid-piece: the region of a sperm flagellum with a mitochondrial sheath, where ATP is generated\ud Oocyte: the egg\ud Outer dense fibers and fibrous sheath: accessory structures reinforcing the mammalian sperm flagellum; the combined axoneme and accessory structures are referred to as 9+9+2\ud Resistive-force theory: an approximation for the local drag of a slender filament element in Stokes flow (or a viscoelastic generalization thereof)\ud Rheotaxis: directed motility in response to the influence of fluid flow\ud Shear: in the context of the flagellum, the relative movement of adjacent microtubule doublets\ud Slender-body theory: an improved approximation for the local drag on a slender filament element in Stokes flow (or a viscoelastic generalization thereof)\ud Zona pellucida: a tough glycoprotein coat between the human egg and the cumulus oophorus, which a sperm must penetrate for successful fertilizatio

    Update on mammalian sperm capacitation : how much does the horse differ from other species?

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    In contrast to various other mammalian species, conventional in vitro fertilization (IVF) with horse gametes is not reliably successful. In particular, stallion spermatozoa fails to penetrate the zona pellucida, most likely due to incomplete activation of stallion spermatozoa (capacitation) under in vitro conditions. In other mammalian species, specific capacitation triggers have been described; unfortunately, none of these is able to induce full capacitation in stallion spermatozoa. Nevertheless, knowledge of capacitation pathways and their molecular triggers might improve our understanding of capacitation-related events observed in stallion sperm. When sperm cells are exposed to appropriate capacitation triggers, several molecular and biochemical changes should be induced in the sperm plasma membrane and cytoplasm. At the level of the sperm plasma membrane, (1) an increase in membrane fluidity, (2) cholesterol depletion and (3) lipid raft aggregation should occur consecutively; the cytoplasmic changes consist of protein tyrosine phosphorylation and elevated pH, cAMP and Ca2+ concentrations. These capacitation-related events enable the switch from progressive to hyperactivated motility of the sperm cells, and the induction of the acrosome reaction. These final capacitation triggers are indispensable for sperm cells to migrate through the viscous oviductal environment, penetrate the cumulus cells and zona pellucida and, finally, fuse with the oolemma. This review will focus on molecular aspects of sperm capacitation and known triggers in various mammalian species. Similarities and differences with the horse will be highlighted to improve our understanding of equine sperm capacitation/fertilizing events

    Finite element simulation for the effect of loading rate on visco-hyperelastic characterisation of soft materials by spherical nanoindentation

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    Nanoindentation test performed by atomic force microscopy is highly recommended for the characterisation of soft materials at nanoscale. The assumption proposed in the characterisation is that the material is pure elastic with no viscosity. However, this assumption does not represent the real characteristics of soft materials such as bio tissues or cells. Therefore, a parametric finite element simulation of nanoindentation by spherical tip was carried out to investigate the response of cells with different constitutive laws (elastic, hyperelastic and visco-hyperelastic). The investigation of the loading rate effect on the characterisation of cell mechanical properties was performed for different size of spherical tips. The selected dimensions of spherical tips cover commercially available products. The viscosity effects are insensitive to the varied dimensions of spherical tip in this study. A limit loading rate was found above which viscous effect has to be considered to correctly determine the mechanical properties. The method in this work can be implemented to propose a criterion for the threshold of loading rate when viscosity effect can be neglected for soft material characterisation

    Role of α/β hydroxylase domain containing protein 2 in stallion sperm activation

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    2019 Fall.Includes bibliographical references.Cell signaling pathways involved in stallion sperm activation are not completely understood. Furthermore, failure of equine in vitro fertilization is commonly attributed to an inability to successfully capacitate sperm. Sperm activation describes the process by which sperm undergo capacitation, hyperactivation, and acrosome reaction in preparation for interaction with an oocyte. 2-arachidonoylglycerol (2AG) is found in the human sperm membrane and prevents calcium influx through the CatSper channel. The α/β hydroxylase domain containing protein 2 (ABHD2) is also found in the human sperm membrane and functions as a progesterone receptor. When progesterone binds to ABHD2, it removes 2AG from the membrane allowing CatSper to open, which leads to calcium entrance into the cell, resulting in sperm activation. It is unclear if this mechanism holds true in stallion. Experiments were conducted to test the hypothesis that progesterone causes sperm activation through interaction with ABHD2 by 1) determining whether the ABHD2 receptor exists on stallion spermatozoa, 2) determining if progesterone binds to ABHD2 on stallion spermatozoa and 3) demonstrating the role of ABHD2 in sperm activation through correlations between ABHD2 and hyperactivation and/or acrosome reaction. Immunoblotting identified ABHD2 protein in stallion sperm and immunocytochemistry (ICC) localized the receptor to the tail region of stallion spermatozoa. Immunocytochemistry also demonstrated that ABHD2 binds progesterone by restricting fluorescence exhibited by ABHD2 when incubated with progesterone. Stallion sperm were evaluated for hyperactivation with computer assisted sperm analysis (CASA) following incubation in capacitation medium with either 1) an endogenous activator of sperm; 3 µM progesterone (P4), 2) a positive pharmacological stimulator of hyperactivation not associated with ABHD2; procaine or 3) a known ABHD2-action inhibitor methyl arachidonyl flourophosphatnate (MAFP). MAFP is a serine hydroxylase inhibitor and functions by preventing the removal of 2AG caused by exposure of ABHD2 to progesterone and, thus, limits hyperactivation. Flow cytometry was used to measure the acrosomal status of treated sperm as a subset of the hyperactivation measurements. When MAFP was administered prior to treatment with either P4 and/or procaine the hyperactive movement was inhibited (p < 0.05) in the presence of P4 but did not affect procaine induced activity. Results were similar for all ejaculates. The reduced hyperactivation of sperm when incubated with both progesterone and MAFP illustrates a potential connection between ABHD2 and CatSper. No change in acrosomal status was discovered through incubation with P4, procaine, or MAFP. These results indicate 1) that ABHD2 is present on stallion sperm, 2) that progesterone binds to ABHD2 and 3) that progesterone has the potential for causing hyperactivation but does not affect the acrosome reaction

    Regulation of motility and Ca2+ signalling in human sperm

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    Human sperm motility is complex, involving several behaviours with different functions. The sperm ‘selects’ and switches between behaviours by using calcium signalling. For example, during the sperm’s transit through the female reproductive tract, it undergoes molecular changes (capacitation, which is absolutely necessary for successful fertilisation). This is accompanied by the adoption of a whiplash-like behaviour called hyperactivation, which enables the sperm to penetrate the oocyte. Many infertile men have sufficient sperm, but their sperm have decreased in motility and/or have failed to adopt the appropriate behaviours, and so they fail to reach and/or fertilise the oocyte. In order to develop a treatment for these cases, it is important to understand the determination and regulation of sperm motility (Alasmari et al.,2013; Tamburrino et al.,2014). In this project, I investigated the effects on human sperm behaviour of the preparation method (conventional density gradient method versus the direct swim up method) and manipulation of Ca2+ store mobilisation and CatSper activation and assessed the efficacy of the different behaviours for penetration through artificial viscous and viscoelastic environments composed of methylcellulose and polyacrylamide. Levels of spontaneously-occurring hyperactivated motility were greater in density-gradient than swim-up prepared cells but swim-up cells performed better in the Kremer penetration test (p<0.005). 4-AP proved a potent inducer of hyperactivated motility but inhibited penetration into viscous medium in cells prepared by both methods

    Experimental Measurement of Human Oocyte Mechanical Properties on a Micro and Nanoforce Sensing Platform Based on Magnetic Springs.

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    International audienceThis article presents a new micro and nanoforce sensor used to perform a mechanical characterisation of human oocytes. This device is based on the use of low-sti_ness magnetic springs. The oocytes to be characterised are placed on a force-sensitive platform. A manipulator equipped with a standard micropipette is used to mechanically compress the oocyte. Some complete \force-compression length" curves associated with mechanical load-unload cycles are given. These curves show the linear, the non-linear and also the plastic mechanical behaviour of the oocytes. These characterisations must be considered as a preliminary result which illustrates that the mechanical variability and the mechanical evolution of human oocytes during their maturation process can be observed with a force sensor based on magnetic springs
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