HPV-16 exposed mouse embryos: a potential model for pregnancy wastage

Purpose Placentas from spontaneous abortions and preterm deliveries have a higher prevalence of Human papillomavirus (HPV) compared to placentas from elective abortions and term births. The objective was to determine the effects of HPV-16 on the adhesion and implantation properties of early embryo t...

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Veröffentlicht in:Archives of gynecology and obstetrics 2013-06, Vol.287 (6), p.1093-1097
Hauptverfasser: Hong, Linda J., Oshiro, Bryan T., Chan, Philip J.
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creator Hong, Linda J.
Oshiro, Bryan T.
Chan, Philip J.
description Purpose Placentas from spontaneous abortions and preterm deliveries have a higher prevalence of Human papillomavirus (HPV) compared to placentas from elective abortions and term births. The objective was to determine the effects of HPV-16 on the adhesion and implantation properties of early embryo trophoblasts. Methods Two-cell mouse embryos were cultured (medium G2, 5 % CO 2 , 37 °C) for 72–96 h and exposed to either HPV-16 rich SiHa cell lysates which were refrigerated after mechanical lysis, thawed lysates which had been frozen for freeze/thaw lysis method, or control medium, incubated (4–5 days) and evaluated by microscopy ( N  = 96 embryos, 3 repeated experiments). Trophoblasts were stained and images were digitized. Adhesion and dimension data were analyzed by Chi-square and t test, respectively. Results HPV-16 exposed embryos exhibited less adhesion through reduced implantation compared with the control (combined lysates 53.8 vs. 85.7 %, P  
doi_str_mv 10.1007/s00404-013-2711-5
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The objective was to determine the effects of HPV-16 on the adhesion and implantation properties of early embryo trophoblasts. Methods Two-cell mouse embryos were cultured (medium G2, 5 % CO 2 , 37 °C) for 72–96 h and exposed to either HPV-16 rich SiHa cell lysates which were refrigerated after mechanical lysis, thawed lysates which had been frozen for freeze/thaw lysis method, or control medium, incubated (4–5 days) and evaluated by microscopy ( N  = 96 embryos, 3 repeated experiments). Trophoblasts were stained and images were digitized. Adhesion and dimension data were analyzed by Chi-square and t test, respectively. Results HPV-16 exposed embryos exhibited less adhesion through reduced implantation compared with the control (combined lysates 53.8 vs. 85.7 %, P  &lt; 0.05). Refrigerated and thawed lysate groups had similar reduced implantations (58.3 vs. 50.0 %). Of the embryos with implantation, 100 % in the refrigerated lysates were noted to have loose or abnormal adhesion. This was measured when embryos were noted to be lost after washes with HTF. There was no difference in trophoblast viability among the groups. Total trophoblast area was greater in the HPV-16 exposed frozen lysate group (1,881.8 ± 605.3 vs. control 848.8 ± 298.0 square units, mean ± SEM). Conclusions HPV-16 inhibited trophoblasts adhesion needed for normal implantation, but not embryo development. Total trophoblast spread was increased after HPV-16 exposure suggesting that HPV-16 altered trophoblast migration. These results suggest that HPV-16 may induce abnormal placental growth resulting in pregnancy wastage.</description><identifier>ISSN: 0932-0067</identifier><identifier>EISSN: 1432-0711</identifier><identifier>DOI: 10.1007/s00404-013-2711-5</identifier><identifier>PMID: 23307167</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Abortion, Spontaneous - virology ; Animals ; Embryo Culture Techniques ; Embryo Implantation ; Embryo Transfer ; Embryo, Mammalian - virology ; Embryonic Development ; Embryos ; Endocrinology ; Female ; Gynecology ; Human Genetics ; Human papillomavirus ; Human papillomavirus 16 - physiology ; Maternal-Fetal Medicine ; Medicine ; Medicine &amp; Public Health ; Mice ; Obstetrics/Perinatology/Midwifery ; Pregnancy ; Trophoblasts - physiology ; Trophoblasts - virology</subject><ispartof>Archives of gynecology and obstetrics, 2013-06, Vol.287 (6), p.1093-1097</ispartof><rights>Springer-Verlag Berlin Heidelberg 2013</rights><rights>Archives of Gynecology and Obstetrics is a copyright of Springer, (2013). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-8098641deb51c256f21461b6d32386b993a9b5c26f6e07fb8a5112ae92477e1d3</citedby><cites>FETCH-LOGICAL-c405t-8098641deb51c256f21461b6d32386b993a9b5c26f6e07fb8a5112ae92477e1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00404-013-2711-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00404-013-2711-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23307167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hong, Linda J.</creatorcontrib><creatorcontrib>Oshiro, Bryan T.</creatorcontrib><creatorcontrib>Chan, Philip J.</creatorcontrib><title>HPV-16 exposed mouse embryos: a potential model for pregnancy wastage</title><title>Archives of gynecology and obstetrics</title><addtitle>Arch Gynecol Obstet</addtitle><addtitle>Arch Gynecol Obstet</addtitle><description>Purpose Placentas from spontaneous abortions and preterm deliveries have a higher prevalence of Human papillomavirus (HPV) compared to placentas from elective abortions and term births. The objective was to determine the effects of HPV-16 on the adhesion and implantation properties of early embryo trophoblasts. Methods Two-cell mouse embryos were cultured (medium G2, 5 % CO 2 , 37 °C) for 72–96 h and exposed to either HPV-16 rich SiHa cell lysates which were refrigerated after mechanical lysis, thawed lysates which had been frozen for freeze/thaw lysis method, or control medium, incubated (4–5 days) and evaluated by microscopy ( N  = 96 embryos, 3 repeated experiments). Trophoblasts were stained and images were digitized. Adhesion and dimension data were analyzed by Chi-square and t test, respectively. Results HPV-16 exposed embryos exhibited less adhesion through reduced implantation compared with the control (combined lysates 53.8 vs. 85.7 %, P  &lt; 0.05). Refrigerated and thawed lysate groups had similar reduced implantations (58.3 vs. 50.0 %). Of the embryos with implantation, 100 % in the refrigerated lysates were noted to have loose or abnormal adhesion. This was measured when embryos were noted to be lost after washes with HTF. There was no difference in trophoblast viability among the groups. Total trophoblast area was greater in the HPV-16 exposed frozen lysate group (1,881.8 ± 605.3 vs. control 848.8 ± 298.0 square units, mean ± SEM). Conclusions HPV-16 inhibited trophoblasts adhesion needed for normal implantation, but not embryo development. Total trophoblast spread was increased after HPV-16 exposure suggesting that HPV-16 altered trophoblast migration. These results suggest that HPV-16 may induce abnormal placental growth resulting in pregnancy wastage.</description><subject>Abortion, Spontaneous - virology</subject><subject>Animals</subject><subject>Embryo Culture Techniques</subject><subject>Embryo Implantation</subject><subject>Embryo Transfer</subject><subject>Embryo, Mammalian - virology</subject><subject>Embryonic Development</subject><subject>Embryos</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Gynecology</subject><subject>Human Genetics</subject><subject>Human papillomavirus</subject><subject>Human papillomavirus 16 - physiology</subject><subject>Maternal-Fetal Medicine</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Mice</subject><subject>Obstetrics/Perinatology/Midwifery</subject><subject>Pregnancy</subject><subject>Trophoblasts - physiology</subject><subject>Trophoblasts - virology</subject><issn>0932-0067</issn><issn>1432-0711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkU1LxDAQhoMo7vrxA7xIwYuX6kzSpI03Eb9gQQ_qNaTtdFnpl0mL7r83y64KgngIkzDPvJOZl7EjhDMESM89QAJJDChiniLGcotNMRE8hvDaZlPQqzuodML2vH8FQJ5lapdNuBABUemUXd89vsSoIvroO09l1HSjp4ia3C07fxHZqO8GaoeFrUOqpDqqOhf1juatbYtl9G79YOd0wHYqW3s63MR99nxz_XR1F88ebu-vLmdxkYAc4gx0phIsKZdYcKkqjonCXJWCi0zlWgurc1lwVSmCtMozKxG5Jc2TNCUsxT47Xev2rnsbyQ-mWfiC6tq2FD5uwvCQKdAS_0eFFCB0OAE9-YW-dqNrwyCGc4VZKkGvBHFNFa7z3lFlerdorFsaBLOyw6ztMMEOs7LDyFBzvFEe84bK74qv_QeArwEfUu2c3E_rv1U_AXKokXI</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Hong, Linda J.</creator><creator>Oshiro, Bryan T.</creator><creator>Chan, Philip J.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20130601</creationdate><title>HPV-16 exposed mouse embryos: a potential model for pregnancy wastage</title><author>Hong, Linda J. ; Oshiro, Bryan T. ; Chan, Philip J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-8098641deb51c256f21461b6d32386b993a9b5c26f6e07fb8a5112ae92477e1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abortion, Spontaneous - virology</topic><topic>Animals</topic><topic>Embryo Culture Techniques</topic><topic>Embryo Implantation</topic><topic>Embryo Transfer</topic><topic>Embryo, Mammalian - virology</topic><topic>Embryonic Development</topic><topic>Embryos</topic><topic>Endocrinology</topic><topic>Female</topic><topic>Gynecology</topic><topic>Human Genetics</topic><topic>Human papillomavirus</topic><topic>Human papillomavirus 16 - physiology</topic><topic>Maternal-Fetal Medicine</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Mice</topic><topic>Obstetrics/Perinatology/Midwifery</topic><topic>Pregnancy</topic><topic>Trophoblasts - physiology</topic><topic>Trophoblasts - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hong, Linda J.</creatorcontrib><creatorcontrib>Oshiro, Bryan T.</creatorcontrib><creatorcontrib>Chan, Philip J.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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The objective was to determine the effects of HPV-16 on the adhesion and implantation properties of early embryo trophoblasts. Methods Two-cell mouse embryos were cultured (medium G2, 5 % CO 2 , 37 °C) for 72–96 h and exposed to either HPV-16 rich SiHa cell lysates which were refrigerated after mechanical lysis, thawed lysates which had been frozen for freeze/thaw lysis method, or control medium, incubated (4–5 days) and evaluated by microscopy ( N  = 96 embryos, 3 repeated experiments). Trophoblasts were stained and images were digitized. Adhesion and dimension data were analyzed by Chi-square and t test, respectively. Results HPV-16 exposed embryos exhibited less adhesion through reduced implantation compared with the control (combined lysates 53.8 vs. 85.7 %, P  &lt; 0.05). Refrigerated and thawed lysate groups had similar reduced implantations (58.3 vs. 50.0 %). Of the embryos with implantation, 100 % in the refrigerated lysates were noted to have loose or abnormal adhesion. This was measured when embryos were noted to be lost after washes with HTF. There was no difference in trophoblast viability among the groups. Total trophoblast area was greater in the HPV-16 exposed frozen lysate group (1,881.8 ± 605.3 vs. control 848.8 ± 298.0 square units, mean ± SEM). Conclusions HPV-16 inhibited trophoblasts adhesion needed for normal implantation, but not embryo development. Total trophoblast spread was increased after HPV-16 exposure suggesting that HPV-16 altered trophoblast migration. These results suggest that HPV-16 may induce abnormal placental growth resulting in pregnancy wastage.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>23307167</pmid><doi>10.1007/s00404-013-2711-5</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Abortion, Spontaneous - virology
Animals
Embryo Culture Techniques
Embryo Implantation
Embryo Transfer
Embryo, Mammalian - virology
Embryonic Development
Embryos
Endocrinology
Female
Gynecology
Human Genetics
Human papillomavirus
Human papillomavirus 16 - physiology
Maternal-Fetal Medicine
Medicine
Medicine & Public Health
Mice
Obstetrics/Perinatology/Midwifery
Pregnancy
Trophoblasts - physiology
Trophoblasts - virology
title HPV-16 exposed mouse embryos: a potential model for pregnancy wastage
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