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Open AccessJournal ArticleDOI

Comparison of the capacitation-like state of cooled boar spermatozoa with true capacitation

CE Green, +1 more
- 01 Dec 2001 - 
- Vol. 122, Iss: 6, pp 889-898
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TLDR
Cooling spermatozoa to 5 degrees C results in a similar endpoint to that observed in capacitated cells in terms of reactive membranes and changes in intracellular ion concentrations, which may account for their comparable functionality.
Abstract
Cryopreserved spermatozoa demonstrate reduced conception rates compared with fresh spermatozoa when used for artificial insemination. The preliminary stage of cryopreservation of spermatozoa involves cooling to 5 degrees C, during which spermatozoa experience a capacitation-like change, which may be partially responsible for the reduced conception rate observed. The aim of this study was to determine the nature of these capacitation-like changes and how much this process resembles true capacitation. Boar spermatozoa, cooled to 5 degrees C and re-warmed to physiological temperatures (39 degrees C), were compared with spermatozoa capacitated in Tyrode's complete medium (TALP) for 2 h at 39 degrees C. Fluorescent probes, and SDS-PAGE and western blotting were used to visualize events known to occur during capacitation in vitro. Chlortetracycline staining of membrane domains and Fluo-3 detection of changes in intracellular free calcium by flow cytometry in cooled and re-warmed spermatozoa showed similarities to those of capacitated spermatozoa. Alterations to lipid bilayer fluidity assessed by merocyanine fluorescence staining and intracellular signalling pathways detected by tyrosine phosphorylation of cooled and re-warmed spermatozoa, did not completely reflect the changes detected during capacitation in vitro. Thus, cooling spermatozoa to 5 degrees C results in a similar endpoint to that observed in capacitated cells in terms of reactive membranes and changes in intracellular ion concentrations, which may account for their comparable functionality. However, these modifications are not completely analogous and should not be considered true capacitation, but rather a by-passing of the capacitation process.

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Citations
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Detection of damage in mammalian sperm cells.

TL;DR: The integrity of sperm DNA can be measured at three different levels by assessing the degree of DNA-protamine condensation, the incidence of breaks and nicks in the DNA and the frequency of fragmentation of the nuclei into sub-haploid apoptotic bodies.
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Flow cytometric evaluation of sperm parameters in relation to fertility potential.

TL;DR: Flow cytometry is a tool that may be used in the future to monitor many new potential markers of sperm function and in conjunction with the flow cytometer, permit the evaluation of a large number of spermatozoa.
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Antioxidant supplementation in vitro improves boar sperm motility and mitochondrial membrane potential after cryopreservation of different fractions of the ejaculate.

TL;DR: In the present trial, exogenous Trolox positively affected post-thaw sperm viability (as motility and mitochondrial membrane potential) in both fractions of the ejaculate.
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Sperm cryopreservation update: Cryodamage, markers, and factors affecting the sperm freezability in pigs.

TL;DR: The present work summarizes the principles of cryoinjury and the relevance of permeating and nonpermeating cryoprotective agents and speculates with new research horizons on the preservation of boar sperm, such as vitrification and freeze-drying.
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Bicarbonate-induced membrane processing in sperm capacitation

TL;DR: It is discovered that bicarbonate induces a rapid collapse of phospholipid transverse asymmetry, exposing phosphatidylethanolamine andosphatidylserine at the outer surface of the lipid bilayer, in conflict with earlier surmises that cholesterol loss precedes activation of the cyclic AMP-protein kinase A axis.
References
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Journal ArticleDOI

Recent developments and concepts in the cryopreservation of spermatozoa and the assessment of their post-thawing function.

TL;DR: The hypothesis is advanced that cryopreserved mammalian spermatozoa are in a state resembling capacitation, which accounts for their relatively reduced longevity and their readiness to undergo egg penetration without incubation.
Journal ArticleDOI

Cold shock damage is due to lipid phase transitions in cell membranes: A demonstration using sperm as a model

TL;DR: The lipid phase behavior was consistent with the temperature range over which cooling was damaging for pig and shrimp sperm, and the with the extent of damage produced in pig and human sperm, the first direct evidence that cold shock results from lipid phase transitions in cell membranes.
Journal ArticleDOI

Determination of the time course of capacitation in mouse spermatozoa using a chlortetracycline fluorescence assay.

TL;DR: The results imply that spermatozoa showing CTC fluorescence pattern B can be considered to be capacitated and that a functional definition for capacitation is the acquired ability to undergo the acrosome reaction rapidly when treated with acid-solubilized zonae pellucidae.
Book ChapterDOI

Fluorescent indicators of ion concentrations.

TL;DR: Ion-concentration gradients across cell membranes are central to any understanding of biological energetics and signal transduction and the characterization of ion gradients requires knowing both extracellular and intracellular ion activities and free concentrations.
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