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Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm
Prohibitin (PHB), a major mitochondrial membrane protein, has been shown earlier in our laboratoryto regulate sperm motility via an alteration in mitochondrial membrane potential (MMP) in infertile men with poor sperm quality. To test if PHB expression is associated with sperm mitochondrial superoxi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192824/ https://www.ncbi.nlm.nih.gov/pubmed/27558591 http://dx.doi.org/10.1111/jcmm.12945 |
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author | Chai, Ran‐Ran Chen, Guo‐Wu Shi, Hui‐Juan O, Wai‐Sum Martin‐DeLeon, Patricia A. Chen, Hong |
author_facet | Chai, Ran‐Ran Chen, Guo‐Wu Shi, Hui‐Juan O, Wai‐Sum Martin‐DeLeon, Patricia A. Chen, Hong |
author_sort | Chai, Ran‐Ran |
collection | PubMed |
description | Prohibitin (PHB), a major mitochondrial membrane protein, has been shown earlier in our laboratoryto regulate sperm motility via an alteration in mitochondrial membrane potential (MMP) in infertile men with poor sperm quality. To test if PHB expression is associated with sperm mitochondrial superoxide (mROS) levels, here we examined sperm mROS levels, high MMP and lipid peroxidation in infertile men with poor sperm motility (asthenospermia, A) and/or low sperm concentrations (oligoasthenospermia, OA). The diaphorase‐type activity of sperm mitochondrial complex I (MCI) and PHB expression were also determined. We demonstrate that mROS and lipid peroxidation levels are significantly higher in sperm from A and OA subjects than in normospermic subjects, whereas high MMP and PHB expression are significantly lower. A positive correlation between mROS and lipid peroxidation and a negative correlation of mROS with PHB expression, high MMP, and sperm motility were found in these subjects. The finding of similar diaphorase‐type activity levels of sperm MCI in the three groups studied suggests that the catalytic subunits of MCI in the matrix arm may produce mROS on its own. There may be a dysfunction of electron transport at MCI associated with decreased expression of PHB in sperm with poor quality. We conclude that mROS level is increased and associated with decreased PHB expression, and it may regulate sperm motility via increases in low MMP and lipid peroxidation. This is the first report on the involvement of PHB in human sperm motility loss associated with increased generation of mROS at MCI. |
format | Online Article Text |
id | pubmed-5192824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51928242017-01-01 Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm Chai, Ran‐Ran Chen, Guo‐Wu Shi, Hui‐Juan O, Wai‐Sum Martin‐DeLeon, Patricia A. Chen, Hong J Cell Mol Med Original Articles Prohibitin (PHB), a major mitochondrial membrane protein, has been shown earlier in our laboratoryto regulate sperm motility via an alteration in mitochondrial membrane potential (MMP) in infertile men with poor sperm quality. To test if PHB expression is associated with sperm mitochondrial superoxide (mROS) levels, here we examined sperm mROS levels, high MMP and lipid peroxidation in infertile men with poor sperm motility (asthenospermia, A) and/or low sperm concentrations (oligoasthenospermia, OA). The diaphorase‐type activity of sperm mitochondrial complex I (MCI) and PHB expression were also determined. We demonstrate that mROS and lipid peroxidation levels are significantly higher in sperm from A and OA subjects than in normospermic subjects, whereas high MMP and PHB expression are significantly lower. A positive correlation between mROS and lipid peroxidation and a negative correlation of mROS with PHB expression, high MMP, and sperm motility were found in these subjects. The finding of similar diaphorase‐type activity levels of sperm MCI in the three groups studied suggests that the catalytic subunits of MCI in the matrix arm may produce mROS on its own. There may be a dysfunction of electron transport at MCI associated with decreased expression of PHB in sperm with poor quality. We conclude that mROS level is increased and associated with decreased PHB expression, and it may regulate sperm motility via increases in low MMP and lipid peroxidation. This is the first report on the involvement of PHB in human sperm motility loss associated with increased generation of mROS at MCI. John Wiley and Sons Inc. 2016-08-25 2017-01 /pmc/articles/PMC5192824/ /pubmed/27558591 http://dx.doi.org/10.1111/jcmm.12945 Text en © 2016 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Chai, Ran‐Ran Chen, Guo‐Wu Shi, Hui‐Juan O, Wai‐Sum Martin‐DeLeon, Patricia A. Chen, Hong Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title | Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title_full | Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title_fullStr | Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title_full_unstemmed | Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title_short | Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm |
title_sort | prohibitin involvement in the generation of mitochondrial superoxide at complex i in human sperm |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192824/ https://www.ncbi.nlm.nih.gov/pubmed/27558591 http://dx.doi.org/10.1111/jcmm.12945 |
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