Cargando…
Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy
Propagation of paternal sperm-contributed mitochondrial genes, resulting in heteroplasmy, is seldom observed in mammals due to post-fertilization degradation of sperm mitochondria, referred to as sperm mitophagy. Whole organelle sperm mitochondrion degradation is thought to be mediated by the interp...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466530/ https://www.ncbi.nlm.nih.gov/pubmed/34572103 http://dx.doi.org/10.3390/cells10092450 |
_version_ | 1784573164731236352 |
---|---|
author | Song, Won-Hee Zuidema, Dalen Yi, Young-Joo Zigo, Michal Zhang, Zhibing Sutovsky, Miriam Sutovsky, Peter |
author_facet | Song, Won-Hee Zuidema, Dalen Yi, Young-Joo Zigo, Michal Zhang, Zhibing Sutovsky, Miriam Sutovsky, Peter |
author_sort | Song, Won-Hee |
collection | PubMed |
description | Propagation of paternal sperm-contributed mitochondrial genes, resulting in heteroplasmy, is seldom observed in mammals due to post-fertilization degradation of sperm mitochondria, referred to as sperm mitophagy. Whole organelle sperm mitochondrion degradation is thought to be mediated by the interplay between the ubiquitin-proteasome system (UPS) and the autophagic pathway (Song et al., Proc. Natl. Acad. Sci. USA, 2016). Both porcine and primate post-fertilization sperm mitophagy rely on the ubiquitin-binding autophagy receptor, sequestosome 1 (SQSTM1), and the proteasome-interacting ubiquitinated protein dislocase, valosin-containing protein (VCP). Consequently, we anticipated that sperm mitophagy could be reconstituted in a cell-free system consisting of permeabilized mammalian spermatozoa co-incubated with porcine oocyte extracts. We found that SQSTM1 was detected in the midpiece/mitochondrial sheath of the sperm tail after, but not before, co-incubation with oocyte extracts. VCP was prominent in the sperm mitochondrial sheath both before and after the extract co-incubation and was also detected in the acrosome and postacrosomal sheath and the subacrosomal layer of the spermatozoa co-incubated with extraction buffer as control. Such patterns are consistent with our previous observation of SQSTM1 and VCP associating with sperm mitochondria inside the porcine zygote. In addition, it was observed that sperm head expansion mimicked the early stages of paternal pronucleus development in a zygote during prolonged sperm-oocyte extract co-incubation. Treatment with anti-SQSTM1 antibody during extract co-incubation prevented ooplasmic SQSTM1 binding to sperm mitochondria. Even in an interspecific cellular environment encompassing bull spermatozoa and porcine oocyte extract, ooplasmic SQSTM1 was recruited to heterospecific sperm mitochondria. Complementary with the binding of SQSTM1 and VCP to sperm mitochondria, two sperm-borne pro-mitophagy proteins, parkin co-regulated gene product (PACRG) and spermatogenesis associated 18 (SPATA18), underwent localization changes after extract coincubation, which were consistent with their degradation observed inside fertilized porcine oocytes. These results demonstrate that the early developmental events of post-fertilization sperm mitophagy observed in porcine zygote can be reconstituted in a cell-free system, which could become a useful tool for identifying additional molecules that regulate mitochondrial inheritance in mammals. |
format | Online Article Text |
id | pubmed-8466530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84665302021-09-27 Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy Song, Won-Hee Zuidema, Dalen Yi, Young-Joo Zigo, Michal Zhang, Zhibing Sutovsky, Miriam Sutovsky, Peter Cells Article Propagation of paternal sperm-contributed mitochondrial genes, resulting in heteroplasmy, is seldom observed in mammals due to post-fertilization degradation of sperm mitochondria, referred to as sperm mitophagy. Whole organelle sperm mitochondrion degradation is thought to be mediated by the interplay between the ubiquitin-proteasome system (UPS) and the autophagic pathway (Song et al., Proc. Natl. Acad. Sci. USA, 2016). Both porcine and primate post-fertilization sperm mitophagy rely on the ubiquitin-binding autophagy receptor, sequestosome 1 (SQSTM1), and the proteasome-interacting ubiquitinated protein dislocase, valosin-containing protein (VCP). Consequently, we anticipated that sperm mitophagy could be reconstituted in a cell-free system consisting of permeabilized mammalian spermatozoa co-incubated with porcine oocyte extracts. We found that SQSTM1 was detected in the midpiece/mitochondrial sheath of the sperm tail after, but not before, co-incubation with oocyte extracts. VCP was prominent in the sperm mitochondrial sheath both before and after the extract co-incubation and was also detected in the acrosome and postacrosomal sheath and the subacrosomal layer of the spermatozoa co-incubated with extraction buffer as control. Such patterns are consistent with our previous observation of SQSTM1 and VCP associating with sperm mitochondria inside the porcine zygote. In addition, it was observed that sperm head expansion mimicked the early stages of paternal pronucleus development in a zygote during prolonged sperm-oocyte extract co-incubation. Treatment with anti-SQSTM1 antibody during extract co-incubation prevented ooplasmic SQSTM1 binding to sperm mitochondria. Even in an interspecific cellular environment encompassing bull spermatozoa and porcine oocyte extract, ooplasmic SQSTM1 was recruited to heterospecific sperm mitochondria. Complementary with the binding of SQSTM1 and VCP to sperm mitochondria, two sperm-borne pro-mitophagy proteins, parkin co-regulated gene product (PACRG) and spermatogenesis associated 18 (SPATA18), underwent localization changes after extract coincubation, which were consistent with their degradation observed inside fertilized porcine oocytes. These results demonstrate that the early developmental events of post-fertilization sperm mitophagy observed in porcine zygote can be reconstituted in a cell-free system, which could become a useful tool for identifying additional molecules that regulate mitochondrial inheritance in mammals. MDPI 2021-09-17 /pmc/articles/PMC8466530/ /pubmed/34572103 http://dx.doi.org/10.3390/cells10092450 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Song, Won-Hee Zuidema, Dalen Yi, Young-Joo Zigo, Michal Zhang, Zhibing Sutovsky, Miriam Sutovsky, Peter Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title | Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title_full | Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title_fullStr | Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title_full_unstemmed | Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title_short | Mammalian Cell-Free System Recapitulates the Early Events of Post-Fertilization Sperm Mitophagy |
title_sort | mammalian cell-free system recapitulates the early events of post-fertilization sperm mitophagy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8466530/ https://www.ncbi.nlm.nih.gov/pubmed/34572103 http://dx.doi.org/10.3390/cells10092450 |
work_keys_str_mv | AT songwonhee mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT zuidemadalen mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT yiyoungjoo mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT zigomichal mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT zhangzhibing mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT sutovskymiriam mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy AT sutovskypeter mammaliancellfreesystemrecapitulatestheearlyeventsofpostfertilizationspermmitophagy |