Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions

Building on our recent discovery of the zinc signature phenomenon present in boar, bull, and human spermatozoa, we have further characterized the role of zinc ions in the spermatozoa’s pathway to fertilization. In boar, the zinc signature differed between the three major boar ejaculate fra...

Full description

Bibliographic Details
Main Authors: Karl Kerns, Momal Sharif, Michal Zigo, Wei Xu, Lauren E. Hamilton, Miriam Sutovsky, Mark Ellersieck, Erma Z. Drobnis, Nicolai Bovin, Richard Oko, David Miller, Peter Sutovsky
Format: Article
Language:English
Published: MDPI AG 2020-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/6/2121
id doaj-212cb55f398045f1b14176eeba4cfb28
record_format Article
spelling doaj-212cb55f398045f1b14176eeba4cfb282020-11-25T01:53:43ZengMDPI AGInternational Journal of Molecular Sciences1422-00672020-03-01216212110.3390/ijms21062121ijms21062121Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida InteractionsKarl Kerns0Momal Sharif1Michal Zigo2Wei Xu3Lauren E. Hamilton4Miriam Sutovsky5Mark Ellersieck6Erma Z. Drobnis7Nicolai Bovin8Richard Oko9David Miller10Peter Sutovsky11Division of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USADepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADivision of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USADepartment of Biomedical and Molecular Sciences, Queen’s University, Kingston, ON K7L 3 N6, CanadaDivision of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USADivision of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USADivision of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USADepartment of Obstetrics, Gynecology and Women’s Health, University of Missouri, Columbia, MO 65211-5300, USAShemyakin Institute of Bioorganic Chemistry, Moscow 117997, RussiaDepartment of Biomedical and Molecular Sciences, Queen’s University, Kingston, ON K7L 3 N6, CanadaDepartment of Animal Sciences, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USADivision of Animal Sciences, University of Missouri, Columbia, MO 65211-5300, USABuilding on our recent discovery of the zinc signature phenomenon present in boar, bull, and human spermatozoa, we have further characterized the role of zinc ions in the spermatozoa’s pathway to fertilization. In boar, the zinc signature differed between the three major boar ejaculate fractions, the initial pre-rich, the sperm-rich, and the post-sperm-rich fraction. These differences set in the sperm ejaculatory sequence establish two major sperm cohorts with marked differences in their sperm capacitation progress. On the subcellular level, we show that the capacitation-induced Zn-ion efflux allows for sperm release from oviductal glycans as analyzed with the oviductal epithelium mimicking glycan binding assay. Sperm zinc efflux also activates zinc-containing enzymes and proteases involved in sperm penetration of the zona pellucida, such as the inner acrosomal membrane matrix metalloproteinase 2 (MMP2). Both MMP2 and the 26S proteasome showed severely reduced activity in the presence of zinc ions, through studies using by gel zymography and the fluorogenic substrates, respectively. In the context of the fertilization-induced oocyte zinc spark and the ensuing oocyte-issued polyspermy-blocking zinc shield, the inhibitory effect of zinc on sperm-borne enzymes may contribute to the fast block of polyspermy. Altogether, our findings establish a new paradigm on the role of zinc ions in sperm function and pave the way for the optimization of animal semen analysis, artificial insemination (AI), and human male-factor infertility diagnostics.https://www.mdpi.com/1422-0067/21/6/2121spermzinccapacitationoviductal reservoirfertilization
collection DOAJ
language English
format Article
sources DOAJ
author Karl Kerns
Momal Sharif
Michal Zigo
Wei Xu
Lauren E. Hamilton
Miriam Sutovsky
Mark Ellersieck
Erma Z. Drobnis
Nicolai Bovin
Richard Oko
David Miller
Peter Sutovsky
spellingShingle Karl Kerns
Momal Sharif
Michal Zigo
Wei Xu
Lauren E. Hamilton
Miriam Sutovsky
Mark Ellersieck
Erma Z. Drobnis
Nicolai Bovin
Richard Oko
David Miller
Peter Sutovsky
Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
International Journal of Molecular Sciences
sperm
zinc
capacitation
oviductal reservoir
fertilization
author_facet Karl Kerns
Momal Sharif
Michal Zigo
Wei Xu
Lauren E. Hamilton
Miriam Sutovsky
Mark Ellersieck
Erma Z. Drobnis
Nicolai Bovin
Richard Oko
David Miller
Peter Sutovsky
author_sort Karl Kerns
title Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
title_short Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
title_full Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
title_fullStr Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
title_full_unstemmed Sperm Cohort-Specific Zinc Signature Acquisition and Capacitation-Induced Zinc Flux Regulate Sperm-Oviduct and Sperm-Zona Pellucida Interactions
title_sort sperm cohort-specific zinc signature acquisition and capacitation-induced zinc flux regulate sperm-oviduct and sperm-zona pellucida interactions
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2020-03-01
description Building on our recent discovery of the zinc signature phenomenon present in boar, bull, and human spermatozoa, we have further characterized the role of zinc ions in the spermatozoa’s pathway to fertilization. In boar, the zinc signature differed between the three major boar ejaculate fractions, the initial pre-rich, the sperm-rich, and the post-sperm-rich fraction. These differences set in the sperm ejaculatory sequence establish two major sperm cohorts with marked differences in their sperm capacitation progress. On the subcellular level, we show that the capacitation-induced Zn-ion efflux allows for sperm release from oviductal glycans as analyzed with the oviductal epithelium mimicking glycan binding assay. Sperm zinc efflux also activates zinc-containing enzymes and proteases involved in sperm penetration of the zona pellucida, such as the inner acrosomal membrane matrix metalloproteinase 2 (MMP2). Both MMP2 and the 26S proteasome showed severely reduced activity in the presence of zinc ions, through studies using by gel zymography and the fluorogenic substrates, respectively. In the context of the fertilization-induced oocyte zinc spark and the ensuing oocyte-issued polyspermy-blocking zinc shield, the inhibitory effect of zinc on sperm-borne enzymes may contribute to the fast block of polyspermy. Altogether, our findings establish a new paradigm on the role of zinc ions in sperm function and pave the way for the optimization of animal semen analysis, artificial insemination (AI), and human male-factor infertility diagnostics.
topic sperm
zinc
capacitation
oviductal reservoir
fertilization
url https://www.mdpi.com/1422-0067/21/6/2121
work_keys_str_mv AT karlkerns spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT momalsharif spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT michalzigo spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT weixu spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT laurenehamilton spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT miriamsutovsky spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT markellersieck spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT ermazdrobnis spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT nicolaibovin spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT richardoko spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT davidmiller spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
AT petersutovsky spermcohortspecificzincsignatureacquisitionandcapacitationinducedzincfluxregulatespermoviductandspermzonapellucidainteractions
_version_ 1724989484037046272