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Improving Freezing Protocols and Organotypic Culture: A Histological Study on Rat Prepubertal Testicular Tissue
Testicular tissue freezing before gonadotoxic treatments allows the preservation of fertility for children suffering from cancer. Recently, the testis organ culture method was presented as a relevant method to restore the fertility of these patients. However, the yield of spermatozoa production is l...
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Published in: | Annals of biomedical engineering 2021-01, Vol.49 (1), p.203-218 |
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creator | Saulnier, Justine Oblette, Antoine Delessard, Marion Dumont, Ludovic Rives, Aurélie Rives, Nathalie Rondanino, Christine |
description | Testicular tissue freezing before gonadotoxic treatments allows the preservation of fertility for children suffering from cancer. Recently, the testis organ culture method was presented as a relevant method to restore the fertility of these patients. However, the yield of spermatozoa production is low in the mouse model and no gamete has been obtained
in vitro
in the rat model. Here, we assess different cryopreservation protocols and culture conditions to improve the efficiency of
in vitro
maturation of rat prepubertal testes. Testes from male rats aged 5 or 8 days
post
-
partum
were cultured onto agarose gels of different percentages. After determining the best culture conditions, different cryopreservation protocols were assessed. Finally, testicular tissues were cultured with media of various compositions and analyzed at different time points. Our results show that the cryopreservation protocols allow the preservation of tissue architecture, cell proliferation, with no or moderate increase of cell death.
In vitro
spermatogenesis did not proceed beyond the pachytene spermatocyte stage. Only 2 of the 6 tested media allowed the survival of differentiated germ cells over the 45-day culture period. In conclusion, this study highlights the necessity to further improve the organ culture method before applying it into the clinics. |
doi_str_mv | 10.1007/s10439-020-02535-8 |
format | article |
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in vitro
in the rat model. Here, we assess different cryopreservation protocols and culture conditions to improve the efficiency of
in vitro
maturation of rat prepubertal testes. Testes from male rats aged 5 or 8 days
post
-
partum
were cultured onto agarose gels of different percentages. After determining the best culture conditions, different cryopreservation protocols were assessed. Finally, testicular tissues were cultured with media of various compositions and analyzed at different time points. Our results show that the cryopreservation protocols allow the preservation of tissue architecture, cell proliferation, with no or moderate increase of cell death.
In vitro
spermatogenesis did not proceed beyond the pachytene spermatocyte stage. Only 2 of the 6 tested media allowed the survival of differentiated germ cells over the 45-day culture period. In conclusion, this study highlights the necessity to further improve the organ culture method before applying it into the clinics.</description><identifier>ISSN: 0090-6964</identifier><identifier>EISSN: 1573-9686</identifier><identifier>DOI: 10.1007/s10439-020-02535-8</identifier><identifier>PMID: 32440757</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Animals ; Biochemistry ; Biological and Medical Physics ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Biophysics ; Cell culture ; Cell death ; Cell differentiation ; Cell Proliferation ; Classical Mechanics ; Cryopreservation ; Fertility ; Freezing ; Gametocytes ; Gels ; Germ cells ; Life Sciences ; Male ; Organ culture ; Organ Culture Techniques ; Original Article ; Pachytene ; Rats ; Rats, Wistar ; Sexual Maturation ; Spermatogenesis ; Spermatozoa ; Testes ; Testis</subject><ispartof>Annals of biomedical engineering, 2021-01, Vol.49 (1), p.203-218</ispartof><rights>Biomedical Engineering Society 2020</rights><rights>Biomedical Engineering Society 2020.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-4761242bc096cbb7e93249ec35c940cf1a68f3b7b9285c96ea87eea2bb75745a3</citedby><cites>FETCH-LOGICAL-c512t-4761242bc096cbb7e93249ec35c940cf1a68f3b7b9285c96ea87eea2bb75745a3</cites><orcidid>0000-0002-1100-9401 ; 0000-0002-5748-6342 ; 0000-0001-9377-5531 ; 0000-0003-2161-0919 ; 0000-0001-6882-6413 ; 0000-0001-9102-1111 ; 0000-0001-7958-8019</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32440757$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://normandie-univ.hal.science/hal-04046432$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Saulnier, Justine</creatorcontrib><creatorcontrib>Oblette, Antoine</creatorcontrib><creatorcontrib>Delessard, Marion</creatorcontrib><creatorcontrib>Dumont, Ludovic</creatorcontrib><creatorcontrib>Rives, Aurélie</creatorcontrib><creatorcontrib>Rives, Nathalie</creatorcontrib><creatorcontrib>Rondanino, Christine</creatorcontrib><title>Improving Freezing Protocols and Organotypic Culture: A Histological Study on Rat Prepubertal Testicular Tissue</title><title>Annals of biomedical engineering</title><addtitle>Ann Biomed Eng</addtitle><addtitle>Ann Biomed Eng</addtitle><description>Testicular tissue freezing before gonadotoxic treatments allows the preservation of fertility for children suffering from cancer. Recently, the testis organ culture method was presented as a relevant method to restore the fertility of these patients. However, the yield of spermatozoa production is low in the mouse model and no gamete has been obtained
in vitro
in the rat model. Here, we assess different cryopreservation protocols and culture conditions to improve the efficiency of
in vitro
maturation of rat prepubertal testes. Testes from male rats aged 5 or 8 days
post
-
partum
were cultured onto agarose gels of different percentages. After determining the best culture conditions, different cryopreservation protocols were assessed. Finally, testicular tissues were cultured with media of various compositions and analyzed at different time points. Our results show that the cryopreservation protocols allow the preservation of tissue architecture, cell proliferation, with no or moderate increase of cell death.
In vitro
spermatogenesis did not proceed beyond the pachytene spermatocyte stage. Only 2 of the 6 tested media allowed the survival of differentiated germ cells over the 45-day culture period. In conclusion, this study highlights the necessity to further improve the organ culture method before applying it into the clinics.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biological and Medical Physics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Biophysics</subject><subject>Cell culture</subject><subject>Cell death</subject><subject>Cell differentiation</subject><subject>Cell Proliferation</subject><subject>Classical Mechanics</subject><subject>Cryopreservation</subject><subject>Fertility</subject><subject>Freezing</subject><subject>Gametocytes</subject><subject>Gels</subject><subject>Germ cells</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Organ culture</subject><subject>Organ Culture Techniques</subject><subject>Original Article</subject><subject>Pachytene</subject><subject>Rats</subject><subject>Rats, 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Mechanics</topic><topic>Cryopreservation</topic><topic>Fertility</topic><topic>Freezing</topic><topic>Gametocytes</topic><topic>Gels</topic><topic>Germ cells</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Organ culture</topic><topic>Organ Culture Techniques</topic><topic>Original Article</topic><topic>Pachytene</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sexual Maturation</topic><topic>Spermatogenesis</topic><topic>Spermatozoa</topic><topic>Testes</topic><topic>Testis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saulnier, Justine</creatorcontrib><creatorcontrib>Oblette, Antoine</creatorcontrib><creatorcontrib>Delessard, Marion</creatorcontrib><creatorcontrib>Dumont, Ludovic</creatorcontrib><creatorcontrib>Rives, Aurélie</creatorcontrib><creatorcontrib>Rives, Nathalie</creatorcontrib><creatorcontrib>Rondanino, 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(HAL)</collection><jtitle>Annals of biomedical engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saulnier, Justine</au><au>Oblette, Antoine</au><au>Delessard, Marion</au><au>Dumont, Ludovic</au><au>Rives, Aurélie</au><au>Rives, Nathalie</au><au>Rondanino, Christine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improving Freezing Protocols and Organotypic Culture: A Histological Study on Rat Prepubertal Testicular Tissue</atitle><jtitle>Annals of biomedical engineering</jtitle><stitle>Ann Biomed Eng</stitle><addtitle>Ann Biomed Eng</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>49</volume><issue>1</issue><spage>203</spage><epage>218</epage><pages>203-218</pages><issn>0090-6964</issn><eissn>1573-9686</eissn><abstract>Testicular tissue freezing before gonadotoxic treatments allows the preservation of fertility for children suffering from cancer. Recently, the testis organ culture method was presented as a relevant method to restore the fertility of these patients. However, the yield of spermatozoa production is low in the mouse model and no gamete has been obtained
in vitro
in the rat model. Here, we assess different cryopreservation protocols and culture conditions to improve the efficiency of
in vitro
maturation of rat prepubertal testes. Testes from male rats aged 5 or 8 days
post
-
partum
were cultured onto agarose gels of different percentages. After determining the best culture conditions, different cryopreservation protocols were assessed. Finally, testicular tissues were cultured with media of various compositions and analyzed at different time points. Our results show that the cryopreservation protocols allow the preservation of tissue architecture, cell proliferation, with no or moderate increase of cell death.
In vitro
spermatogenesis did not proceed beyond the pachytene spermatocyte stage. Only 2 of the 6 tested media allowed the survival of differentiated germ cells over the 45-day culture period. In conclusion, this study highlights the necessity to further improve the organ culture method before applying it into the clinics.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>32440757</pmid><doi>10.1007/s10439-020-02535-8</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-1100-9401</orcidid><orcidid>https://orcid.org/0000-0002-5748-6342</orcidid><orcidid>https://orcid.org/0000-0001-9377-5531</orcidid><orcidid>https://orcid.org/0000-0003-2161-0919</orcidid><orcidid>https://orcid.org/0000-0001-6882-6413</orcidid><orcidid>https://orcid.org/0000-0001-9102-1111</orcidid><orcidid>https://orcid.org/0000-0001-7958-8019</orcidid></addata></record> |
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subjects | Animals Biochemistry Biological and Medical Physics Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Biophysics Cell culture Cell death Cell differentiation Cell Proliferation Classical Mechanics Cryopreservation Fertility Freezing Gametocytes Gels Germ cells Life Sciences Male Organ culture Organ Culture Techniques Original Article Pachytene Rats Rats, Wistar Sexual Maturation Spermatogenesis Spermatozoa Testes Testis |
title | Improving Freezing Protocols and Organotypic Culture: A Histological Study on Rat Prepubertal Testicular Tissue |
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