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Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions

BACKGROUND: The mammalian epididymis is responsible for the provision of a highly specialized environment in which spermatozoa acquire functional maturity and are subsequently stored in preparation for ejaculation. Making important contributions to both processes are epididymosomes, small extracellu...

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Autores principales: Zhou, Wei, Stanger, Simone J., Anderson, Amanda L., Bernstein, Ilana R., De Iuliis, Geoffry N., McCluskey, Adam, McLaughlin, Eileen A., Dun, Matthew D., Nixon, Brett
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474069/
https://www.ncbi.nlm.nih.gov/pubmed/30999907
http://dx.doi.org/10.1186/s12915-019-0653-5
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author Zhou, Wei
Stanger, Simone J.
Anderson, Amanda L.
Bernstein, Ilana R.
De Iuliis, Geoffry N.
McCluskey, Adam
McLaughlin, Eileen A.
Dun, Matthew D.
Nixon, Brett
author_facet Zhou, Wei
Stanger, Simone J.
Anderson, Amanda L.
Bernstein, Ilana R.
De Iuliis, Geoffry N.
McCluskey, Adam
McLaughlin, Eileen A.
Dun, Matthew D.
Nixon, Brett
author_sort Zhou, Wei
collection PubMed
description BACKGROUND: The mammalian epididymis is responsible for the provision of a highly specialized environment in which spermatozoa acquire functional maturity and are subsequently stored in preparation for ejaculation. Making important contributions to both processes are epididymosomes, small extracellular vesicles released from the epididymal soma via an apocrine secretory pathway. While considerable effort has been focused on defining the cargo transferred between epididymosomes and spermatozoa, comparatively less is known about the mechanistic basis of these interactions. To investigate this phenomenon, we have utilized an in vitro co-culture system to track the transfer of biotinylated protein cargo between mouse epididymosomes and recipient spermatozoa isolated from the caput epididymis; an epididymal segment that is of critical importance for promoting sperm maturation. RESULTS: Our data indicate that epididymosome-sperm interactions are initiated via tethering of the epididymosome to receptors restricted to the post-acrosomal domain of the sperm head. Thereafter, epididymosomes mediate the transfer of protein cargo to spermatozoa via a process that is dependent on dynamin, a family of mechanoenzymes that direct intercellular vesicle trafficking. Notably, upon co-culture of sperm with epididymosomes, dynamin 1 undergoes a pronounced relocation between the peri- and post-acrosomal domains of the sperm head. This repositioning of dynamin 1 is potentially mediated via its association with membrane rafts and ideally locates the enzyme to facilitate the uptake of epididymosome-borne proteins. Accordingly, disruption of membrane raft integrity or pharmacological inhibition of dynamin both potently suppress the transfer of biotinylated epididymosome proteins to spermatozoa. CONCLUSION: Together, these data provide new mechanistic insight into epididymosome-sperm interactions with potential implications extending to the manipulation of sperm maturation for the purpose of fertility regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0653-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-64740692019-04-24 Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions Zhou, Wei Stanger, Simone J. Anderson, Amanda L. Bernstein, Ilana R. De Iuliis, Geoffry N. McCluskey, Adam McLaughlin, Eileen A. Dun, Matthew D. Nixon, Brett BMC Biol Research Article BACKGROUND: The mammalian epididymis is responsible for the provision of a highly specialized environment in which spermatozoa acquire functional maturity and are subsequently stored in preparation for ejaculation. Making important contributions to both processes are epididymosomes, small extracellular vesicles released from the epididymal soma via an apocrine secretory pathway. While considerable effort has been focused on defining the cargo transferred between epididymosomes and spermatozoa, comparatively less is known about the mechanistic basis of these interactions. To investigate this phenomenon, we have utilized an in vitro co-culture system to track the transfer of biotinylated protein cargo between mouse epididymosomes and recipient spermatozoa isolated from the caput epididymis; an epididymal segment that is of critical importance for promoting sperm maturation. RESULTS: Our data indicate that epididymosome-sperm interactions are initiated via tethering of the epididymosome to receptors restricted to the post-acrosomal domain of the sperm head. Thereafter, epididymosomes mediate the transfer of protein cargo to spermatozoa via a process that is dependent on dynamin, a family of mechanoenzymes that direct intercellular vesicle trafficking. Notably, upon co-culture of sperm with epididymosomes, dynamin 1 undergoes a pronounced relocation between the peri- and post-acrosomal domains of the sperm head. This repositioning of dynamin 1 is potentially mediated via its association with membrane rafts and ideally locates the enzyme to facilitate the uptake of epididymosome-borne proteins. Accordingly, disruption of membrane raft integrity or pharmacological inhibition of dynamin both potently suppress the transfer of biotinylated epididymosome proteins to spermatozoa. CONCLUSION: Together, these data provide new mechanistic insight into epididymosome-sperm interactions with potential implications extending to the manipulation of sperm maturation for the purpose of fertility regulation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12915-019-0653-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-18 /pmc/articles/PMC6474069/ /pubmed/30999907 http://dx.doi.org/10.1186/s12915-019-0653-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhou, Wei
Stanger, Simone J.
Anderson, Amanda L.
Bernstein, Ilana R.
De Iuliis, Geoffry N.
McCluskey, Adam
McLaughlin, Eileen A.
Dun, Matthew D.
Nixon, Brett
Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title_full Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title_fullStr Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title_full_unstemmed Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title_short Mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
title_sort mechanisms of tethering and cargo transfer during epididymosome-sperm interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6474069/
https://www.ncbi.nlm.nih.gov/pubmed/30999907
http://dx.doi.org/10.1186/s12915-019-0653-5
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