Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg

Human epididymal sperm protein ARP, a member of the cysteine-rich secretory proteins (CRISP) family, exhibits significant homology with rat epididymal protein DE, a candidate molecule for mediating sperm-egg fusion in rodents. The aim of this study was to investigate the involvement of ARP in human...

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Publicado: 2001
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00063363_v65_n4_p1000_Cohen
http://hdl.handle.net/20.500.12110/paper_00063363_v65_n4_p1000_Cohen
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spelling paper:paper_00063363_v65_n4_p1000_Cohen2023-06-08T14:31:02Z Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg Epididymis Fertilization Gamete biology Ovum Sperm calcium ionophore human epididymal sperm protein ARP polyclonal antibody rat epididymal sperm protein DE recombinant protein secretory protein unclassified drug acrosome reaction animal cell article cell fusion cell viability concentration response controlled study extraction female fertilization hamster human human cell immunofluorescence male metabolic inhibition nonhuman normal human oocyte priority journal sequence homology sperm spermatozoon capacitation spermatozoon motility spermatozoon penetration surface property zona pellucida Human epididymal sperm protein ARP, a member of the cysteine-rich secretory proteins (CRISP) family, exhibits significant homology with rat epididymal protein DE, a candidate molecule for mediating sperm-egg fusion in rodents. The aim of this study was to investigate the involvement of ARP in human gamete fusion. Sequential extraction of proteins from ejaculated human sperm revealed the existence of a population of ARP that is tightly associated with the sperm surface and thus, potentially capable of participating in gamete interaction. Exposure of capacitated human sperm to a polyclonal antibody against recombinant ARP (anti-ARP) produced a significant and concentration-dependent inhibition in the ability of human sperm to penetrate zona-free hamster eggs. This inhibition was not due to a deleterious effect on the gametes because anti-ARP affected neither sperm viability or motility, nor egg penetrability. The antibody did not inhibit the occurrence of spontaneous or Ca 2+ ionophore-induced acrosome reaction, nor did it inhibit the ability of sperm to bind to the oolema, supporting a specific inhibition of the antibody at the sperm-egg fusion level. As a relevant evidence for a role of ARP in gamete fusion, the existence of complementary sites for this protein on the surface of human eggs was investigated. Experiments in which zona-free human oocytes discarded from in vitro fertilization programs were exposed to ARP, fixed, and subjected to indirect immunofluorescence revealed the presence of specific ARP-binding sites on the entire surface of the human egg, in agreement with the fusogenic properties of the human oolema. Together, these results strongly support the participation of ARP in the sperm-egg fusion process, suggesting that this protein would be the functional homologue of DE in humans. 2001 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00063363_v65_n4_p1000_Cohen http://hdl.handle.net/20.500.12110/paper_00063363_v65_n4_p1000_Cohen
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Epididymis
Fertilization
Gamete biology
Ovum
Sperm
calcium ionophore
human epididymal sperm protein ARP
polyclonal antibody
rat epididymal sperm protein DE
recombinant protein
secretory protein
unclassified drug
acrosome reaction
animal cell
article
cell fusion
cell viability
concentration response
controlled study
extraction
female
fertilization
hamster
human
human cell
immunofluorescence
male
metabolic inhibition
nonhuman
normal human
oocyte
priority journal
sequence homology
sperm
spermatozoon capacitation
spermatozoon motility
spermatozoon penetration
surface property
zona pellucida
spellingShingle Epididymis
Fertilization
Gamete biology
Ovum
Sperm
calcium ionophore
human epididymal sperm protein ARP
polyclonal antibody
rat epididymal sperm protein DE
recombinant protein
secretory protein
unclassified drug
acrosome reaction
animal cell
article
cell fusion
cell viability
concentration response
controlled study
extraction
female
fertilization
hamster
human
human cell
immunofluorescence
male
metabolic inhibition
nonhuman
normal human
oocyte
priority journal
sequence homology
sperm
spermatozoon capacitation
spermatozoon motility
spermatozoon penetration
surface property
zona pellucida
Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
topic_facet Epididymis
Fertilization
Gamete biology
Ovum
Sperm
calcium ionophore
human epididymal sperm protein ARP
polyclonal antibody
rat epididymal sperm protein DE
recombinant protein
secretory protein
unclassified drug
acrosome reaction
animal cell
article
cell fusion
cell viability
concentration response
controlled study
extraction
female
fertilization
hamster
human
human cell
immunofluorescence
male
metabolic inhibition
nonhuman
normal human
oocyte
priority journal
sequence homology
sperm
spermatozoon capacitation
spermatozoon motility
spermatozoon penetration
surface property
zona pellucida
description Human epididymal sperm protein ARP, a member of the cysteine-rich secretory proteins (CRISP) family, exhibits significant homology with rat epididymal protein DE, a candidate molecule for mediating sperm-egg fusion in rodents. The aim of this study was to investigate the involvement of ARP in human gamete fusion. Sequential extraction of proteins from ejaculated human sperm revealed the existence of a population of ARP that is tightly associated with the sperm surface and thus, potentially capable of participating in gamete interaction. Exposure of capacitated human sperm to a polyclonal antibody against recombinant ARP (anti-ARP) produced a significant and concentration-dependent inhibition in the ability of human sperm to penetrate zona-free hamster eggs. This inhibition was not due to a deleterious effect on the gametes because anti-ARP affected neither sperm viability or motility, nor egg penetrability. The antibody did not inhibit the occurrence of spontaneous or Ca 2+ ionophore-induced acrosome reaction, nor did it inhibit the ability of sperm to bind to the oolema, supporting a specific inhibition of the antibody at the sperm-egg fusion level. As a relevant evidence for a role of ARP in gamete fusion, the existence of complementary sites for this protein on the surface of human eggs was investigated. Experiments in which zona-free human oocytes discarded from in vitro fertilization programs were exposed to ARP, fixed, and subjected to indirect immunofluorescence revealed the presence of specific ARP-binding sites on the entire surface of the human egg, in agreement with the fusogenic properties of the human oolema. Together, these results strongly support the participation of ARP in the sperm-egg fusion process, suggesting that this protein would be the functional homologue of DE in humans.
title Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
title_short Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
title_full Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
title_fullStr Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
title_full_unstemmed Evidence that human epididymal protein ARP plays a role in gamete fusion through complementary sites on the surface of the human egg
title_sort evidence that human epididymal protein arp plays a role in gamete fusion through complementary sites on the surface of the human egg
publishDate 2001
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00063363_v65_n4_p1000_Cohen
http://hdl.handle.net/20.500.12110/paper_00063363_v65_n4_p1000_Cohen
_version_ 1768541683440418816