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Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli

Human sperm show a variety of different behaviours (types of motility) that have different functional roles. Previous reports suggest that sperm may reversibly switch between these behaviours. We have recorded and analysed the behaviour of individual human sperm (180 cells in total), each cell monit...

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Autores principales: Achikanu, Cosmas, Correia, Joao, Guidobaldi, Héctor A, Giojalas, Laura C, Barratt, Christopher L R, Da Silva, Sarah Martins, Publicover, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736438/
https://www.ncbi.nlm.nih.gov/pubmed/31194869
http://dx.doi.org/10.1093/molehr/gaz034
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author Achikanu, Cosmas
Correia, Joao
Guidobaldi, Héctor A
Giojalas, Laura C
Barratt, Christopher L R
Da Silva, Sarah Martins
Publicover, Stephen
author_facet Achikanu, Cosmas
Correia, Joao
Guidobaldi, Héctor A
Giojalas, Laura C
Barratt, Christopher L R
Da Silva, Sarah Martins
Publicover, Stephen
author_sort Achikanu, Cosmas
collection PubMed
description Human sperm show a variety of different behaviours (types of motility) that have different functional roles. Previous reports suggest that sperm may reversibly switch between these behaviours. We have recorded and analysed the behaviour of individual human sperm (180 cells in total), each cell monitored continuously for 3–3.5 min either under control conditions or in the presence of Ca(2+)-mobilising stimuli. Switching between different behaviours was assessed visually (1 s bins using four behaviour categories), and was verified by fractal dimension analysis of sperm head tracks. In the absence of stimuli, ~90% of cells showed at least one behavioural transition (mean rate under control conditions = 6.4 ± 0.8 transitions.min(−1)). Type 1 behaviour (progressive, activated-like motility) was most common, but the majority of cells (>70%) displayed at least three behaviour types. Treatment of sperm with Ca(2+)-mobilising agonists had negligible effects on the rate of switching but increased the time spent in type 2 and type 3 (hyperactivation-like) behaviours (P < 2(*)10(−8); chi-square). Treatment with 4-aminopyridine under alkaline conditions (pH(o) = 8.5), a highly-potent Ca(2+)-mobilising stimulus, was the most effective in increasing the proportion of type 3 behaviour, biasing switching away from type 1 (P < 0.005) and dramatically extending the duration of type 3 events (P < 10(−16)). Other stimuli, including 300 nM progesterone and 1% human follicular fluid, had qualitatively similar effects but were less potent. We conclude that human sperm observed in vitro constitutively display a range of behaviours and regulation of motility by [Ca(2+)](i), at the level of the single cell, is achieved not by causing cells to adopt a ‘new’ behaviour but by changing the relative contributions of those behaviours.
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spelling pubmed-67364382019-09-16 Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli Achikanu, Cosmas Correia, Joao Guidobaldi, Héctor A Giojalas, Laura C Barratt, Christopher L R Da Silva, Sarah Martins Publicover, Stephen Mol Hum Reprod Editor's Choice Human sperm show a variety of different behaviours (types of motility) that have different functional roles. Previous reports suggest that sperm may reversibly switch between these behaviours. We have recorded and analysed the behaviour of individual human sperm (180 cells in total), each cell monitored continuously for 3–3.5 min either under control conditions or in the presence of Ca(2+)-mobilising stimuli. Switching between different behaviours was assessed visually (1 s bins using four behaviour categories), and was verified by fractal dimension analysis of sperm head tracks. In the absence of stimuli, ~90% of cells showed at least one behavioural transition (mean rate under control conditions = 6.4 ± 0.8 transitions.min(−1)). Type 1 behaviour (progressive, activated-like motility) was most common, but the majority of cells (>70%) displayed at least three behaviour types. Treatment of sperm with Ca(2+)-mobilising agonists had negligible effects on the rate of switching but increased the time spent in type 2 and type 3 (hyperactivation-like) behaviours (P < 2(*)10(−8); chi-square). Treatment with 4-aminopyridine under alkaline conditions (pH(o) = 8.5), a highly-potent Ca(2+)-mobilising stimulus, was the most effective in increasing the proportion of type 3 behaviour, biasing switching away from type 1 (P < 0.005) and dramatically extending the duration of type 3 events (P < 10(−16)). Other stimuli, including 300 nM progesterone and 1% human follicular fluid, had qualitatively similar effects but were less potent. We conclude that human sperm observed in vitro constitutively display a range of behaviours and regulation of motility by [Ca(2+)](i), at the level of the single cell, is achieved not by causing cells to adopt a ‘new’ behaviour but by changing the relative contributions of those behaviours. Oxford University Press 2019-06-13 /pmc/articles/PMC6736438/ /pubmed/31194869 http://dx.doi.org/10.1093/molehr/gaz034 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editor's Choice
Achikanu, Cosmas
Correia, Joao
Guidobaldi, Héctor A
Giojalas, Laura C
Barratt, Christopher L R
Da Silva, Sarah Martins
Publicover, Stephen
Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title_full Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title_fullStr Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title_full_unstemmed Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title_short Continuous behavioural ‘switching’ in human spermatozoa and its regulation by Ca(2+)-mobilising stimuli
title_sort continuous behavioural ‘switching’ in human spermatozoa and its regulation by ca(2+)-mobilising stimuli
topic Editor's Choice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736438/
https://www.ncbi.nlm.nih.gov/pubmed/31194869
http://dx.doi.org/10.1093/molehr/gaz034
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