Not all sperm are equal: functional mitochondria characterize a subpopulation of human sperm with better fertilization potential
Human sperm samples are very heterogeneous and include a low amount of truly functional gametes. Distinct strategies have been developed to characterize and isolate this specific subpopulation. In this study we have used fluorescence microscopy and fluorescence-activated cell sorting to determine if...
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creator | Sousa, Ana Paula Amaral, Alexandra Baptista, Marta Tavares, Renata Caballero Campo, Pedro Caballero Peregrín, Pedro Freitas, Albertina Paiva, Artur Almeida-Santos, Teresa Ramalho-Santos, João |
description | Human sperm samples are very heterogeneous and include a low amount of truly functional gametes. Distinct strategies have been developed to characterize and isolate this specific subpopulation. In this study we have used fluorescence microscopy and fluorescence-activated cell sorting to determine if mitochondrial function, as assessed using mitochondrial-sensitive probes, could be employed as a criterion to obtain more functional sperm from a given ejaculate. We first determined that mitochondrial activity correlated with the quality of distinct human samples, from healthy donors to patients with decreased semen quality. Furthermore, using fluorescence-activated cell sorting to separate sperm with active and inactive mitochondria we found that this was also true within samples. Indeed, sperm with active mitochondria defined a more functional subpopulation, which contained more capacitated and acrosome intact cells, sperm with lower chromatin damage, and, crucially, sperm more able to decondense and participate in early development using both chemical induction and injection into mature bovine oocytes. Furthermore, cell sorting using mitochondrial activity produced a more functional sperm subpopulation than classic swim-up, both in terms of improvement in a variety of functional sperm parameters and in statistical significance. In conclusion, whatever the true biological role of sperm mitochondria in fertilization, mitochondrial activity is a clear hallmark of human sperm functionality. |
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Distinct strategies have been developed to characterize and isolate this specific subpopulation. In this study we have used fluorescence microscopy and fluorescence-activated cell sorting to determine if mitochondrial function, as assessed using mitochondrial-sensitive probes, could be employed as a criterion to obtain more functional sperm from a given ejaculate. We first determined that mitochondrial activity correlated with the quality of distinct human samples, from healthy donors to patients with decreased semen quality. Furthermore, using fluorescence-activated cell sorting to separate sperm with active and inactive mitochondria we found that this was also true within samples. Indeed, sperm with active mitochondria defined a more functional subpopulation, which contained more capacitated and acrosome intact cells, sperm with lower chromatin damage, and, crucially, sperm more able to decondense and participate in early development using both chemical induction and injection into mature bovine oocytes. Furthermore, cell sorting using mitochondrial activity produced a more functional sperm subpopulation than classic swim-up, both in terms of improvement in a variety of functional sperm parameters and in statistical significance. In conclusion, whatever the true biological role of sperm mitochondria in fertilization, mitochondrial activity is a clear hallmark of human sperm functionality.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0018112</identifier><identifier>PMID: 21448461</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Aldehydes - metabolism ; Animals ; Biology ; Cattle ; Cell Fractionation ; Cell Separation ; Chromatin ; Chromatin - metabolism ; Fertilization ; Fertilization - physiology ; Flow Cytometry ; Fluorescence ; Fluorescence microscopy ; Gametes ; Humans ; Laboratories ; Life sciences ; Male ; Medicine ; Metaphase ; Microscopy ; Mitochondria ; Mitochondria - metabolism ; Motility ; Neurosciences ; Oocytes ; Oocytes - metabolism ; Semen ; Sperm ; Sperm Motility - physiology ; Spermatozoa - metabolism ; Staining and Labeling ; Statistical analysis ; Statistical methods</subject><ispartof>PloS one, 2011-03, Vol.6 (3), p.e18112-e18112</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Sousa et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Distinct strategies have been developed to characterize and isolate this specific subpopulation. In this study we have used fluorescence microscopy and fluorescence-activated cell sorting to determine if mitochondrial function, as assessed using mitochondrial-sensitive probes, could be employed as a criterion to obtain more functional sperm from a given ejaculate. We first determined that mitochondrial activity correlated with the quality of distinct human samples, from healthy donors to patients with decreased semen quality. Furthermore, using fluorescence-activated cell sorting to separate sperm with active and inactive mitochondria we found that this was also true within samples. 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In conclusion, whatever the true biological role of sperm mitochondria in fertilization, mitochondrial activity is a clear hallmark of human sperm functionality.</description><subject>Aldehydes - metabolism</subject><subject>Animals</subject><subject>Biology</subject><subject>Cattle</subject><subject>Cell Fractionation</subject><subject>Cell Separation</subject><subject>Chromatin</subject><subject>Chromatin - metabolism</subject><subject>Fertilization</subject><subject>Fertilization - physiology</subject><subject>Flow Cytometry</subject><subject>Fluorescence</subject><subject>Fluorescence microscopy</subject><subject>Gametes</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Life sciences</subject><subject>Male</subject><subject>Medicine</subject><subject>Metaphase</subject><subject>Microscopy</subject><subject>Mitochondria</subject><subject>Mitochondria - metabolism</subject><subject>Motility</subject><subject>Neurosciences</subject><subject>Oocytes</subject><subject>Oocytes - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sousa, Ana Paula</au><au>Amaral, Alexandra</au><au>Baptista, Marta</au><au>Tavares, Renata</au><au>Caballero Campo, Pedro</au><au>Caballero Peregrín, Pedro</au><au>Freitas, Albertina</au><au>Paiva, Artur</au><au>Almeida-Santos, Teresa</au><au>Ramalho-Santos, João</au><au>Clarke, Hugh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Not all sperm are equal: functional mitochondria characterize a subpopulation of human sperm with better fertilization potential</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2011-03-23</date><risdate>2011</risdate><volume>6</volume><issue>3</issue><spage>e18112</spage><epage>e18112</epage><pages>e18112-e18112</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Human sperm samples are very heterogeneous and include a low amount of truly functional gametes. Distinct strategies have been developed to characterize and isolate this specific subpopulation. In this study we have used fluorescence microscopy and fluorescence-activated cell sorting to determine if mitochondrial function, as assessed using mitochondrial-sensitive probes, could be employed as a criterion to obtain more functional sperm from a given ejaculate. We first determined that mitochondrial activity correlated with the quality of distinct human samples, from healthy donors to patients with decreased semen quality. Furthermore, using fluorescence-activated cell sorting to separate sperm with active and inactive mitochondria we found that this was also true within samples. Indeed, sperm with active mitochondria defined a more functional subpopulation, which contained more capacitated and acrosome intact cells, sperm with lower chromatin damage, and, crucially, sperm more able to decondense and participate in early development using both chemical induction and injection into mature bovine oocytes. Furthermore, cell sorting using mitochondrial activity produced a more functional sperm subpopulation than classic swim-up, both in terms of improvement in a variety of functional sperm parameters and in statistical significance. In conclusion, whatever the true biological role of sperm mitochondria in fertilization, mitochondrial activity is a clear hallmark of human sperm functionality.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21448461</pmid><doi>10.1371/journal.pone.0018112</doi><tpages>e18112</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aldehydes - metabolism Animals Biology Cattle Cell Fractionation Cell Separation Chromatin Chromatin - metabolism Fertilization Fertilization - physiology Flow Cytometry Fluorescence Fluorescence microscopy Gametes Humans Laboratories Life sciences Male Medicine Metaphase Microscopy Mitochondria Mitochondria - metabolism Motility Neurosciences Oocytes Oocytes - metabolism Semen Sperm Sperm Motility - physiology Spermatozoa - metabolism Staining and Labeling Statistical analysis Statistical methods |
title | Not all sperm are equal: functional mitochondria characterize a subpopulation of human sperm with better fertilization potential |
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