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HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility

Reverse cholesterol transport or cholesterol efflux is part of an extensive plasma membrane remodeling process in spermatozoa that is imperative for fertilization. For ram spermatozoa, sheep serum is well known to support in vitro fertilization (IVF), but knowledge of its explicit role is limited. T...

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Autores principales: Bernecic, Naomi C, de Graaf, Simon P, Leahy, Tamara, Gadella, Bart M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181994/
https://www.ncbi.nlm.nih.gov/pubmed/33674849
http://dx.doi.org/10.1093/biolre/ioab035
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author Bernecic, Naomi C
de Graaf, Simon P
Leahy, Tamara
Gadella, Bart M
author_facet Bernecic, Naomi C
de Graaf, Simon P
Leahy, Tamara
Gadella, Bart M
author_sort Bernecic, Naomi C
collection PubMed
description Reverse cholesterol transport or cholesterol efflux is part of an extensive plasma membrane remodeling process in spermatozoa that is imperative for fertilization. For ram spermatozoa, sheep serum is well known to support in vitro fertilization (IVF), but knowledge of its explicit role is limited. Though, it is postulated to elicit cholesterol efflux owing to the presence of high-density lipoproteins (HDLs) that interact with transmembrane cholesterol transporters, such as adenosinetriphosphate (ATP)-binding cassette transporter A1 (ABCA1) and scavenger receptor class B, type I (SR-BI). In this study, we report that both sheep serum and HDLs were able to elicit cholesterol efflux alone by up to 20–40% (as measured by the boron dipyrromethene (BODIPY)-cholesterol assay). Furthermore, when the antagonists glibenclamide and valspodar were used to inhibit the function of ABCA1 and SR-BI or ABCA1 alone, respectively, cholesterol efflux was only marginally reduced (8–15%). Nevertheless, it is likely that in ram spermatozoa, a specific facilitated pathway of cholesterol efflux is involved in the interaction between cholesterol acceptors and transporters. Interestingly, exposure to HDLs also induced hyperactivated motility, another critical event required for successful fertilization. Taken together, this study details the first report of the dual action of HDLs on ram spermatozoa, providing both an insight into the intricacy of events leading up to fertilization in vivo as well as demonstrating the possible application of HDL supplementation in media for IVF.
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spelling pubmed-81819942021-06-07 HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility Bernecic, Naomi C de Graaf, Simon P Leahy, Tamara Gadella, Bart M Biol Reprod Research Article Reverse cholesterol transport or cholesterol efflux is part of an extensive plasma membrane remodeling process in spermatozoa that is imperative for fertilization. For ram spermatozoa, sheep serum is well known to support in vitro fertilization (IVF), but knowledge of its explicit role is limited. Though, it is postulated to elicit cholesterol efflux owing to the presence of high-density lipoproteins (HDLs) that interact with transmembrane cholesterol transporters, such as adenosinetriphosphate (ATP)-binding cassette transporter A1 (ABCA1) and scavenger receptor class B, type I (SR-BI). In this study, we report that both sheep serum and HDLs were able to elicit cholesterol efflux alone by up to 20–40% (as measured by the boron dipyrromethene (BODIPY)-cholesterol assay). Furthermore, when the antagonists glibenclamide and valspodar were used to inhibit the function of ABCA1 and SR-BI or ABCA1 alone, respectively, cholesterol efflux was only marginally reduced (8–15%). Nevertheless, it is likely that in ram spermatozoa, a specific facilitated pathway of cholesterol efflux is involved in the interaction between cholesterol acceptors and transporters. Interestingly, exposure to HDLs also induced hyperactivated motility, another critical event required for successful fertilization. Taken together, this study details the first report of the dual action of HDLs on ram spermatozoa, providing both an insight into the intricacy of events leading up to fertilization in vivo as well as demonstrating the possible application of HDL supplementation in media for IVF. Oxford University Press 2021-03-01 /pmc/articles/PMC8181994/ /pubmed/33674849 http://dx.doi.org/10.1093/biolre/ioab035 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Society for the Study of Reproduction. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Bernecic, Naomi C
de Graaf, Simon P
Leahy, Tamara
Gadella, Bart M
HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title_full HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title_fullStr HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title_full_unstemmed HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title_short HDL mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
title_sort hdl mediates reverse cholesterol transport from ram spermatozoa and induces hyperactivated motility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8181994/
https://www.ncbi.nlm.nih.gov/pubmed/33674849
http://dx.doi.org/10.1093/biolre/ioab035
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