Literature DB >> 28175305

The roles of protein disulphide isomerase family A, member 3 (ERp57) and surface thiol/disulphide exchange in human spermatozoa-zona pellucida binding.

Chi-Wai Wong1, Kevin K W Lam1,2,3, Cheuk-Lun Lee1,2,3, William S B Yeung1,2,3, Wei E Zhao4, Pak-Chung Ho1,2,3, Jian-Ping Ou5, Philip C N Chiu1,2,3.   

Abstract

Study question: Are multimeric sperm plasma membrane protein complexes, ERp57 and sperm surface thiol content involved in human spermatozoa-zona pellucida (ZP) interaction? Summary answer: ERp57 is a component of a multimeric spermatozoa-ZP receptor complex involved in regulation of human spermatozoa-ZP binding via up-regulation of sperm surface thiol content. What is known already: A spermatozoon acquires its fertilization capacity within the female reproductive tract by capacitation. Spermatozoa-ZP receptor is suggested to be a composite structure that is assembled into a functional complex during capacitation. Sperm surface thiol content is elevated during capacitation. ERp57 is a protein disulphide isomerase that modulates the thiol-disulphide status of proteins. Study design, size, duration: The binding ability and components of protein complexes in extracted membrane protein fractions of spermatozoa were studied. The roles of capacitation, thiol-disulphide reagent treatments and ERp57 on sperm functions and sperm surface thiol content were assessed. Participants/materials, setting, methods: Spermatozoa were obtained from semen samples from normozoospermic men. Human oocytes were obtained from an assisted reproduction programme. Blue native polyacrylamide gel electrophoresis, western ligand blotting and mass spectrometry were used to identify the components of solubilized ZP/ZP3-binding complexes. The localization and expression of sperm surface thiol and ERp57 were studied by immunostaining and sperm surface protein biotinylation followed by western blotting. Sperm functions were assessed by standard assays. Main results and the role of chance: Several ZP-binding complexes were isolated from the cell membrane of capacitated spermatozoa. ERp57 was a component of one of these complexes. Capacitation significantly increased the sperm surface thiol content, acrosomal thiol distribution and ERp57 expression on sperm surface. Sperm surface thiol and ERp57 immunoreactivity were localized to the acrosomal region of spermatozoa, a region responsible for ZP-binding. Up-regulation of the surface thiol content or ERp57 surface expression in vitro stimulated ZP-binding capacity of human spermatozoa. Blocking of ERp57 function by specific antibody or inhibitors against ERp57 reduced the surface thiol content and ZP-binding capacity of human spermatozoa. Large scale data: N/A. Limitations, reasons for caution: The mechanisms by which up-regulation of surface thiol content stimulates spermatozoa-ZP binding have not been depicted. Wider implications of the findings: Thiol-disulphide exchange is a crucial event in capacitation. ERp57 modulates the event and the subsequent fertilization process. Modulation of the surface thiol content of the spermatozoa of subfertile men may help to increase fertilization rate in assisted reproduction. Study funding/competing interest(s): This work was supported by The Hong Kong Research Grant Council Grant HKU764611 and HKU764512M to P.C.N.C. The authors have no competing interests.
© The Author 2017. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com

Entities:  

Keywords:  ERp57; PDIA3; capacitation; fertilization; sperm function; thiol-disulphide exchange; zona pellucida

Mesh:

Substances:

Year:  2017        PMID: 28175305     DOI: 10.1093/humrep/dex007

Source DB:  PubMed          Journal:  Hum Reprod        ISSN: 0268-1161            Impact factor:   6.918


  5 in total

1.  The proteome of frozen-thawed pig spermatozoa is dependent on the ejaculate fraction source.

Authors:  Cristina Pérez-Patiño; Junwei Li; Isabel Barranco; Emilio A Martínez; Heriberto Rodriguez-Martínez; Jordi Roca; Inmaculada Parrilla
Journal:  Sci Rep       Date:  2019-01-24       Impact factor: 4.379

2.  Spatiotemporal profiling of the bovine oviduct fluid proteome around the time of ovulation.

Authors:  Coline Mahé; Régis Lavigne; Emmanuelle Com; Charles Pineau; Yann Locatelli; Aleksandra Maria Zlotkowska; Carmen Almiñana; Guillaume Tsikis; Pascal Mermillod; Jennifer Schoen; Marie Saint-Dizier
Journal:  Sci Rep       Date:  2022-03-09       Impact factor: 4.379

3.  Peroxiredoxin 6 Peroxidase and Ca2+-Independent Phospholipase A2 Activities Are Essential to Support Male-Mouse Fertility.

Authors:  Edrian Bumanlag; Eleonora Scarlata; Cristian O'Flaherty
Journal:  Antioxidants (Basel)       Date:  2022-01-25

4.  Sperm Proteome after Interaction with Reproductive Fluids in Porcine: From the Ejaculation to the Fertilization Site.

Authors:  Chiara Luongo; Leopoldo González-Brusi; Paula Cots-Rodríguez; Mª José Izquierdo-Rico; Manuel Avilés; Francisco Alberto García-Vázquez
Journal:  Int J Mol Sci       Date:  2020-08-22       Impact factor: 5.923

Review 5.  ERp57/PDIA3: new insight.

Authors:  Silvia Chichiarelli; Fabio Altieri; Giuliano Paglia; Elisabetta Rubini; Marco Minacori; Margherita Eufemi
Journal:  Cell Mol Biol Lett       Date:  2022-02-02       Impact factor: 5.787

  5 in total

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