Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media
Purpose Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability. Methods Cow ovarian fragments were i...
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Veröffentlicht in: | Journal of assisted reproduction and genetics 2020-10, Vol.37 (10), p.2477-2486 |
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creator | Vilela, Janice de M. V. Dolmans, Marie-Madeleine Maruhashi, Emi Blackman, Marine C. N. M. Sonveaux, Pierre Miranda-Vilela, Ana Luisa Amorim, Christiani A. |
description | Purpose
Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability.
Methods
Cow ovarian fragments were immersed in 0.9% NaCl solution, IVF medium, Leibovitz 15 medium (L-15), or PBS for 1, 4, or 24 h at 4 °C. Media were analyzed for pH, lactate dehydrogenase (LDH) activity, and glucose, pyruvate, and lactate concentrations, while apoptosis was assessed by TUNEL assays in fixed fragments. Viability rates were assessed by flow cytometry (FACS).
Results
There were lower pH levels in NaCl at all time points compared with other media. LDH activity increased with time and was lowest in NaCl at 1 and 4 h. There was no significant difference in glucose levels, but a significant pyruvate decrease in L-15 and a significant lactate increase in all media. TUNEL showed apoptosis rates ranging from 0 to 5%. FACS showed a mean of 4% necrotic cells and 15–19% apoptotic cells after 1 h of incubation, but less than 1% necrotic cells and 2–6% apoptotic cells after 24 h in all media.
Conclusion
Our results indicate marked metabolic activity in ovarian tissue at 4 °C and suggest that cells use internal sources of energy, which may influence transplantation outcomes. This highlights the importance of better understanding whole tissue dynamics to develop a standard protocol for ovarian tissue transportation.
Graphical abstract |
doi_str_mv | 10.1007/s10815-020-01935-y |
format | Article |
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Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability.
Methods
Cow ovarian fragments were immersed in 0.9% NaCl solution, IVF medium, Leibovitz 15 medium (L-15), or PBS for 1, 4, or 24 h at 4 °C. Media were analyzed for pH, lactate dehydrogenase (LDH) activity, and glucose, pyruvate, and lactate concentrations, while apoptosis was assessed by TUNEL assays in fixed fragments. Viability rates were assessed by flow cytometry (FACS).
Results
There were lower pH levels in NaCl at all time points compared with other media. LDH activity increased with time and was lowest in NaCl at 1 and 4 h. There was no significant difference in glucose levels, but a significant pyruvate decrease in L-15 and a significant lactate increase in all media. TUNEL showed apoptosis rates ranging from 0 to 5%. FACS showed a mean of 4% necrotic cells and 15–19% apoptotic cells after 1 h of incubation, but less than 1% necrotic cells and 2–6% apoptotic cells after 24 h in all media.
Conclusion
Our results indicate marked metabolic activity in ovarian tissue at 4 °C and suggest that cells use internal sources of energy, which may influence transplantation outcomes. This highlights the importance of better understanding whole tissue dynamics to develop a standard protocol for ovarian tissue transportation.
Graphical abstract</description><identifier>ISSN: 1058-0468</identifier><identifier>EISSN: 1573-7330</identifier><identifier>DOI: 10.1007/s10815-020-01935-y</identifier><identifier>PMID: 32885380</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Fertility Preservation ; Gynecology ; Human Genetics ; Medicine ; Medicine & Public Health ; Reproductive Medicine</subject><ispartof>Journal of assisted reproduction and genetics, 2020-10, Vol.37 (10), p.2477-2486</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-6a07a6eb8619e45de000cefbfe4489427e5cebb7b22145fb99e6a196046c3e863</citedby><cites>FETCH-LOGICAL-c489t-6a07a6eb8619e45de000cefbfe4489427e5cebb7b22145fb99e6a196046c3e863</cites><orcidid>0000-0003-1794-0368 ; 0000-0003-1840-9974 ; 0000-0002-6331-3026 ; 0000-0002-4762-8757 ; 0000-0001-6484-8834</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550475/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550475/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids></links><search><creatorcontrib>Vilela, Janice de M. V.</creatorcontrib><creatorcontrib>Dolmans, Marie-Madeleine</creatorcontrib><creatorcontrib>Maruhashi, Emi</creatorcontrib><creatorcontrib>Blackman, Marine C. N. M.</creatorcontrib><creatorcontrib>Sonveaux, Pierre</creatorcontrib><creatorcontrib>Miranda-Vilela, Ana Luisa</creatorcontrib><creatorcontrib>Amorim, Christiani A.</creatorcontrib><title>Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media</title><title>Journal of assisted reproduction and genetics</title><addtitle>J Assist Reprod Genet</addtitle><description>Purpose
Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability.
Methods
Cow ovarian fragments were immersed in 0.9% NaCl solution, IVF medium, Leibovitz 15 medium (L-15), or PBS for 1, 4, or 24 h at 4 °C. Media were analyzed for pH, lactate dehydrogenase (LDH) activity, and glucose, pyruvate, and lactate concentrations, while apoptosis was assessed by TUNEL assays in fixed fragments. Viability rates were assessed by flow cytometry (FACS).
Results
There were lower pH levels in NaCl at all time points compared with other media. LDH activity increased with time and was lowest in NaCl at 1 and 4 h. There was no significant difference in glucose levels, but a significant pyruvate decrease in L-15 and a significant lactate increase in all media. TUNEL showed apoptosis rates ranging from 0 to 5%. FACS showed a mean of 4% necrotic cells and 15–19% apoptotic cells after 1 h of incubation, but less than 1% necrotic cells and 2–6% apoptotic cells after 24 h in all media.
Conclusion
Our results indicate marked metabolic activity in ovarian tissue at 4 °C and suggest that cells use internal sources of energy, which may influence transplantation outcomes. This highlights the importance of better understanding whole tissue dynamics to develop a standard protocol for ovarian tissue transportation.
Graphical abstract</description><subject>Fertility Preservation</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Reproductive Medicine</subject><issn>1058-0468</issn><issn>1573-7330</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9UU1v1TAQtBCoLaV_gJOPXAzrr8S5IKGqfEiVuNCz5Tib4irPDrYT9P59XV6FxIXTrrQzs7M7hLzl8J4D9B8KB8M1AwEM-CA1O74gF1z3kvVSwsvWgzYMVGfOyetSHgBgMEKekXMpjNHSwAWZbvYwYfRI00wPWN2YluCp8zXsoR7ptOUQ7-mSfrOKhxWzq1tu4N3l4CKtoZQN6ZqxYN5dDSnSEOkU5hkzxtokp-DekFezWwpePddLcvf55sf1V3b7_cu360-3zCszVNY56F2Ho-n4gEpP2Ax7nMcZVZsr0aP2OI79KARXeh6HATvHh65d6CWaTl6SjyfddRvbYt8MZLfYNYeDy0ebXLD_TmL4ae_TbnutQfW6Cbx7Fsjp14al2kMoHpfFRUxbsUKphpNaigYVJ6jPqZSM8981HOxTPPYUj23x2D_x2GMjyROprE9vxWwf0pZj-8n_WI-EgZV3</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Vilela, Janice de M. V.</creator><creator>Dolmans, Marie-Madeleine</creator><creator>Maruhashi, Emi</creator><creator>Blackman, Marine C. N. M.</creator><creator>Sonveaux, Pierre</creator><creator>Miranda-Vilela, Ana Luisa</creator><creator>Amorim, Christiani A.</creator><general>Springer US</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1794-0368</orcidid><orcidid>https://orcid.org/0000-0003-1840-9974</orcidid><orcidid>https://orcid.org/0000-0002-6331-3026</orcidid><orcidid>https://orcid.org/0000-0002-4762-8757</orcidid><orcidid>https://orcid.org/0000-0001-6484-8834</orcidid></search><sort><creationdate>20201001</creationdate><title>Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media</title><author>Vilela, Janice de M. V. ; Dolmans, Marie-Madeleine ; Maruhashi, Emi ; Blackman, Marine C. N. M. ; Sonveaux, Pierre ; Miranda-Vilela, Ana Luisa ; Amorim, Christiani A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-6a07a6eb8619e45de000cefbfe4489427e5cebb7b22145fb99e6a196046c3e863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Fertility Preservation</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Reproductive Medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vilela, Janice de M. V.</creatorcontrib><creatorcontrib>Dolmans, Marie-Madeleine</creatorcontrib><creatorcontrib>Maruhashi, Emi</creatorcontrib><creatorcontrib>Blackman, Marine C. N. M.</creatorcontrib><creatorcontrib>Sonveaux, Pierre</creatorcontrib><creatorcontrib>Miranda-Vilela, Ana Luisa</creatorcontrib><creatorcontrib>Amorim, Christiani A.</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of assisted reproduction and genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vilela, Janice de M. V.</au><au>Dolmans, Marie-Madeleine</au><au>Maruhashi, Emi</au><au>Blackman, Marine C. N. M.</au><au>Sonveaux, Pierre</au><au>Miranda-Vilela, Ana Luisa</au><au>Amorim, Christiani A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media</atitle><jtitle>Journal of assisted reproduction and genetics</jtitle><stitle>J Assist Reprod Genet</stitle><date>2020-10-01</date><risdate>2020</risdate><volume>37</volume><issue>10</issue><spage>2477</spage><epage>2486</epage><pages>2477-2486</pages><issn>1058-0468</issn><eissn>1573-7330</eissn><abstract>Purpose
Although ovarian tissue transportation has been validated for up to 24 h, there is no standard protocol to date. We aimed to elucidate how existing media currently used for ovarian tissue transportation affect ovarian tissue metabolism and cell viability.
Methods
Cow ovarian fragments were immersed in 0.9% NaCl solution, IVF medium, Leibovitz 15 medium (L-15), or PBS for 1, 4, or 24 h at 4 °C. Media were analyzed for pH, lactate dehydrogenase (LDH) activity, and glucose, pyruvate, and lactate concentrations, while apoptosis was assessed by TUNEL assays in fixed fragments. Viability rates were assessed by flow cytometry (FACS).
Results
There were lower pH levels in NaCl at all time points compared with other media. LDH activity increased with time and was lowest in NaCl at 1 and 4 h. There was no significant difference in glucose levels, but a significant pyruvate decrease in L-15 and a significant lactate increase in all media. TUNEL showed apoptosis rates ranging from 0 to 5%. FACS showed a mean of 4% necrotic cells and 15–19% apoptotic cells after 1 h of incubation, but less than 1% necrotic cells and 2–6% apoptotic cells after 24 h in all media.
Conclusion
Our results indicate marked metabolic activity in ovarian tissue at 4 °C and suggest that cells use internal sources of energy, which may influence transplantation outcomes. This highlights the importance of better understanding whole tissue dynamics to develop a standard protocol for ovarian tissue transportation.
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subjects | Fertility Preservation Gynecology Human Genetics Medicine Medicine & Public Health Reproductive Medicine |
title | Evidence of metabolic activity during low-temperature ovarian tissue preservation in different media |
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