Maternal tract factors contribute to paternal seminal fluid impact on metabolic phenotype in offspring
Paternal characteristics and exposures influence physiology and disease risks in progeny, but the mechanisms are mostly unknown. Seminal fluid, which affects female reproductive tract gene expression as well as sperm survival and integrity, provides one potential pathway. We evaluated in mice the co...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2014-02, Vol.111 (6), p.2200-2205 |
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description | Paternal characteristics and exposures influence physiology and disease risks in progeny, but the mechanisms are mostly unknown. Seminal fluid, which affects female reproductive tract gene expression as well as sperm survival and integrity, provides one potential pathway. We evaluated in mice the consequences for offspring of ablating the plasma fraction of seminal fluid by surgical excision of the seminal vesicle gland. Conception was substantially impaired and, when pregnancy did occur, placental hypertrophy was evident in late gestation. After birth, the growth trajectory and metabolic parameters of progeny were altered, most profoundly in males, which exhibited obesity, distorted metabolic hormones, reduced glucose tolerance, and hypertension. Altered offspring phenotype was partly attributable to sperm damage and partly to an effect of seminal fluid deficiency on the female tract, because increased adiposity was also evident in adult male progeny when normal two-cell embryos were transferred to females mated with seminal vesicle-excised males. Moreover, embryos developed in female tracts not exposed to seminal plasma were abnormal from the early cleavage stages, but culture in vitro partly alleviated this. Absence of seminal plasma was accompanied by down-regulation of the embryotrophic factors Lif, Csf2, Il6, and Egf and up-regulation of the apoptosis-inducing factor Trail in the oviduct. These findings show that paternal seminal fluid composition affects the growth and health of male offspring, and reveal that its impact on the periconception environment involves not only sperm protection but also indirect effects on preimplantation embryos via oviduct expression of embryotrophic cytokines. |
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Seminal fluid, which affects female reproductive tract gene expression as well as sperm survival and integrity, provides one potential pathway. We evaluated in mice the consequences for offspring of ablating the plasma fraction of seminal fluid by surgical excision of the seminal vesicle gland. Conception was substantially impaired and, when pregnancy did occur, placental hypertrophy was evident in late gestation. After birth, the growth trajectory and metabolic parameters of progeny were altered, most profoundly in males, which exhibited obesity, distorted metabolic hormones, reduced glucose tolerance, and hypertension. Altered offspring phenotype was partly attributable to sperm damage and partly to an effect of seminal fluid deficiency on the female tract, because increased adiposity was also evident in adult male progeny when normal two-cell embryos were transferred to females mated with seminal vesicle-excised males. Moreover, embryos developed in female tracts not exposed to seminal plasma were abnormal from the early cleavage stages, but culture in vitro partly alleviated this. Absence of seminal plasma was accompanied by down-regulation of the embryotrophic factors Lif, Csf2, Il6, and Egf and up-regulation of the apoptosis-inducing factor Trail in the oviduct. These findings show that paternal seminal fluid composition affects the growth and health of male offspring, and reveal that its impact on the periconception environment involves not only sperm protection but also indirect effects on preimplantation embryos via oviduct expression of embryotrophic cytokines.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1305609111</identifier><identifier>PMID: 24469827</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>adiposity ; adults ; Animals ; Apoptosis ; Biological Sciences ; Blastocyst ; Blood Pressure ; conception ; Cytokines ; Embryos ; Epigenetics ; excision ; Female ; females ; Gene expression ; Genitalia, Female - physiology ; Genotype & phenotype ; glucose tolerance ; hormones ; hypertension ; hypertrophy ; in vitro culture ; interleukin-6 ; Male ; males ; Mating behavior ; Metabolism ; Mice ; Mice, Inbred BALB C ; Mice, Inbred CBA ; obesity ; Oviducts ; Phenotype ; pregnancy ; progeny ; risk ; Semen ; Seminal plasma ; seminal vesicles ; Spermatozoa ; Survival analysis ; Zygotes</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (6), p.2200-2205</ispartof><rights>copyright © 1993–2008 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Feb 11, 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c565t-259b18ff302e71b06ba3d664a56bff1effa722f0532dfae064e8f76077d1d3073</citedby><cites>FETCH-LOGICAL-c565t-259b18ff302e71b06ba3d664a56bff1effa722f0532dfae064e8f76077d1d3073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/111/6.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23768840$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23768840$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24469827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bromfield, John J.</creatorcontrib><creatorcontrib>Schjenken, John E.</creatorcontrib><creatorcontrib>Chin, Peck Y.</creatorcontrib><creatorcontrib>Care, Alison S.</creatorcontrib><creatorcontrib>Jasper, Melinda J.</creatorcontrib><creatorcontrib>Robertson, Sarah A.</creatorcontrib><title>Maternal tract factors contribute to paternal seminal fluid impact on metabolic phenotype in offspring</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Paternal characteristics and exposures influence physiology and disease risks in progeny, but the mechanisms are mostly unknown. Seminal fluid, which affects female reproductive tract gene expression as well as sperm survival and integrity, provides one potential pathway. We evaluated in mice the consequences for offspring of ablating the plasma fraction of seminal fluid by surgical excision of the seminal vesicle gland. Conception was substantially impaired and, when pregnancy did occur, placental hypertrophy was evident in late gestation. After birth, the growth trajectory and metabolic parameters of progeny were altered, most profoundly in males, which exhibited obesity, distorted metabolic hormones, reduced glucose tolerance, and hypertension. Altered offspring phenotype was partly attributable to sperm damage and partly to an effect of seminal fluid deficiency on the female tract, because increased adiposity was also evident in adult male progeny when normal two-cell embryos were transferred to females mated with seminal vesicle-excised males. Moreover, embryos developed in female tracts not exposed to seminal plasma were abnormal from the early cleavage stages, but culture in vitro partly alleviated this. Absence of seminal plasma was accompanied by down-regulation of the embryotrophic factors Lif, Csf2, Il6, and Egf and up-regulation of the apoptosis-inducing factor Trail in the oviduct. These findings show that paternal seminal fluid composition affects the growth and health of male offspring, and reveal that its impact on the periconception environment involves not only sperm protection but also indirect effects on preimplantation embryos via oviduct expression of embryotrophic cytokines.</description><subject>adiposity</subject><subject>adults</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological Sciences</subject><subject>Blastocyst</subject><subject>Blood Pressure</subject><subject>conception</subject><subject>Cytokines</subject><subject>Embryos</subject><subject>Epigenetics</subject><subject>excision</subject><subject>Female</subject><subject>females</subject><subject>Gene expression</subject><subject>Genitalia, Female - physiology</subject><subject>Genotype & phenotype</subject><subject>glucose tolerance</subject><subject>hormones</subject><subject>hypertension</subject><subject>hypertrophy</subject><subject>in vitro culture</subject><subject>interleukin-6</subject><subject>Male</subject><subject>males</subject><subject>Mating behavior</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred CBA</subject><subject>obesity</subject><subject>Oviducts</subject><subject>Phenotype</subject><subject>pregnancy</subject><subject>progeny</subject><subject>risk</subject><subject>Semen</subject><subject>Seminal plasma</subject><subject>seminal vesicles</subject><subject>Spermatozoa</subject><subject>Survival analysis</subject><subject>Zygotes</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1TAQhS0EopfCmhXIEhs2acfvZIOEKl5SERtYW05it75K7GA7lfrvcXTb28KGjcfSfOdoZg5CrwmcEVDsfAkmnxEGQkJHCHmCdqR-Gsk7eIp2AFQ1Laf8BL3IeQ8AnWjhOTqhnMuupWqH3HdTbApmwiWZoWBXn5gyHmIoyfdrsbhEvNxD2c5-q25a_Yj9vGyaGPBsi-nj5Ae8XNsQy-1isQ84OpeX5MPVS_TMmSnbV3f1FP36_Onnxdfm8seXbxcfL5tBSFEaKrqetM4xoFaRHmRv2CglN0L2zhHrnFGUOhCMjs5YkNy2TklQaiQjqwc5RR8Ovsvaz3YcbN3CTLrOMJt0q6Px-u9O8Nf6Kt5o1lEJLa8G7-8MUvy92lz07PNgp8kEG9esSQuMMCkl_T_Ku46wjosNffcPuo_rdtADBUIoKip1fqCGFHNO1h3nJqC3uPUWt36IuyrePl73yN_n-wjYlEc7QrTUlAJU4M0B2Oea-4MBU7JtObA_Qq-7lQ</recordid><startdate>20140211</startdate><enddate>20140211</enddate><creator>Bromfield, John J.</creator><creator>Schjenken, John E.</creator><creator>Chin, Peck Y.</creator><creator>Care, Alison S.</creator><creator>Jasper, Melinda J.</creator><creator>Robertson, Sarah A.</creator><general>National Academy of Sciences</general><general>National Acad Sciences</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20140211</creationdate><title>Maternal tract factors contribute to paternal seminal fluid impact on metabolic phenotype in offspring</title><author>Bromfield, John J. ; 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Seminal fluid, which affects female reproductive tract gene expression as well as sperm survival and integrity, provides one potential pathway. We evaluated in mice the consequences for offspring of ablating the plasma fraction of seminal fluid by surgical excision of the seminal vesicle gland. Conception was substantially impaired and, when pregnancy did occur, placental hypertrophy was evident in late gestation. After birth, the growth trajectory and metabolic parameters of progeny were altered, most profoundly in males, which exhibited obesity, distorted metabolic hormones, reduced glucose tolerance, and hypertension. Altered offspring phenotype was partly attributable to sperm damage and partly to an effect of seminal fluid deficiency on the female tract, because increased adiposity was also evident in adult male progeny when normal two-cell embryos were transferred to females mated with seminal vesicle-excised males. Moreover, embryos developed in female tracts not exposed to seminal plasma were abnormal from the early cleavage stages, but culture in vitro partly alleviated this. Absence of seminal plasma was accompanied by down-regulation of the embryotrophic factors Lif, Csf2, Il6, and Egf and up-regulation of the apoptosis-inducing factor Trail in the oviduct. These findings show that paternal seminal fluid composition affects the growth and health of male offspring, and reveal that its impact on the periconception environment involves not only sperm protection but also indirect effects on preimplantation embryos via oviduct expression of embryotrophic cytokines.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>24469827</pmid><doi>10.1073/pnas.1305609111</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adiposity adults Animals Apoptosis Biological Sciences Blastocyst Blood Pressure conception Cytokines Embryos Epigenetics excision Female females Gene expression Genitalia, Female - physiology Genotype & phenotype glucose tolerance hormones hypertension hypertrophy in vitro culture interleukin-6 Male males Mating behavior Metabolism Mice Mice, Inbred BALB C Mice, Inbred CBA obesity Oviducts Phenotype pregnancy progeny risk Semen Seminal plasma seminal vesicles Spermatozoa Survival analysis Zygotes |
title | Maternal tract factors contribute to paternal seminal fluid impact on metabolic phenotype in offspring |
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