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Gamete therapeutics: recombinant protein adsorption by sperm for increasing fertility via artificial insemination
A decrease in fertility can have a negative economic impact, both locally and over a broader geographical scope, and this is especially the case with regard to the cattle industry. Therefore, much interest exists in evaluating proteins that might be able to increase the fertility of sperm. Heparin b...
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Published in: | PloS one 2013-06, Vol.8 (6), p.e65083-e65083 |
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creator | Alvarez-Gallardo, Horacio Kjelland, Michael E Moreno, Juan F Welsh, Jr, Thomas H Randel, Ronald D Lammoglia, Miguel A Pérez-Martínez, Mario Lara-Sagahón, Alma V Esperón-Sumano, A Enrique Romo, Salvador |
description | A decrease in fertility can have a negative economic impact, both locally and over a broader geographical scope, and this is especially the case with regard to the cattle industry. Therefore, much interest exists in evaluating proteins that might be able to increase the fertility of sperm. Heparin binding proteins (HBPs), specifically the fertility associated antigen (FAA) and the Type-2 tissue inhibitor of metalloproteinase (TIMP-2), act to favor the capacitation and acrosome reaction and perhaps even modulate the immune system's response toward the sperm. The objective of this research was to determine the effect on fertility of adding recombinant FAA (rFAA) and recombinant TIMP-2 (rTIMP-2) to bovine semen before cryopreservation for use in an artificial insemination (AI) program in a tropical environment. For this experiment, 100 crossbred (Bos taurus x Bos indicus) heifers were selected based on their estrus cycle, body condition score (BCS), of 4 to 6 on a scale of 1 to 9, and adequate anatomical conformation evaluated by pelvic and genital (normal) measurements. Heifers were synchronized using estradiol benzoate (EB), Celosil® (PGF2α) (Shering-Plough) and a controlled internal drug release (CIDR) device was inserted that contained progesterone. Inseminations were performed in two groups at random, 50 animals per group. The control group was inseminated with conventional semen. The treatment group was inseminated with semen containing rFAA (25 µg/mL) and rTIMP-2 (25 µg/mL). In the control group a 16% pregnancy rate was obtained versus a 40% pregnancy rate for the HBP treatment group, resulting in a significant difference (P = 0.0037). Given the results herein, one may conclude that the HBPs can increase fertility and could be an option for cattle in tropical conditions; however, one needs to consider the environment, nutrition, and the genetic interaction affecting the final result in whatever reproductive program that is implemented. |
doi_str_mv | 10.1371/journal.pone.0065083 |
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Therefore, much interest exists in evaluating proteins that might be able to increase the fertility of sperm. Heparin binding proteins (HBPs), specifically the fertility associated antigen (FAA) and the Type-2 tissue inhibitor of metalloproteinase (TIMP-2), act to favor the capacitation and acrosome reaction and perhaps even modulate the immune system's response toward the sperm. The objective of this research was to determine the effect on fertility of adding recombinant FAA (rFAA) and recombinant TIMP-2 (rTIMP-2) to bovine semen before cryopreservation for use in an artificial insemination (AI) program in a tropical environment. For this experiment, 100 crossbred (Bos taurus x Bos indicus) heifers were selected based on their estrus cycle, body condition score (BCS), of 4 to 6 on a scale of 1 to 9, and adequate anatomical conformation evaluated by pelvic and genital (normal) measurements. Heifers were synchronized using estradiol benzoate (EB), Celosil® (PGF2α) (Shering-Plough) and a controlled internal drug release (CIDR) device was inserted that contained progesterone. Inseminations were performed in two groups at random, 50 animals per group. The control group was inseminated with conventional semen. The treatment group was inseminated with semen containing rFAA (25 µg/mL) and rTIMP-2 (25 µg/mL). In the control group a 16% pregnancy rate was obtained versus a 40% pregnancy rate for the HBP treatment group, resulting in a significant difference (P = 0.0037). Given the results herein, one may conclude that the HBPs can increase fertility and could be an option for cattle in tropical conditions; however, one needs to consider the environment, nutrition, and the genetic interaction affecting the final result in whatever reproductive program that is implemented.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0065083</identifier><identifier>PMID: 23762288</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>17β-Estradiol ; Acrosome reaction ; Adsorption ; Agriculture ; Animals ; Anticoagulants ; Artificial insemination ; Beef ; Binding proteins ; Biology ; Bovidae ; Capacitation ; Cattle ; Cryopreservation ; Drug delivery systems ; Economic impact ; Estrus cycle ; Estrus Synchronization ; Female ; Fertility ; Fertility - physiology ; Fluorescent Antibody Technique, Indirect ; Heparin ; Humans ; Immune system ; Impact analysis ; Insemination, Artificial ; Laboratory animals ; Male ; Males ; Membrane Proteins - administration & dosage ; Membrane Proteins - metabolism ; Metalloproteinase ; Nutrition ; Ovulation ; Plasma ; Pregnancy ; Pregnancy Rate ; Progesterone ; Prostate ; Protein adsorption ; Protein binding ; Proteins ; Recombinant proteins ; Recombinant Proteins - administration & dosage ; Recombinant Proteins - metabolism ; Reproduction (biology) ; Semen ; Semen - metabolism ; Sex hormones ; Sperm ; Spermatozoa - metabolism ; Tissue inhibitor of metalloproteinase 2 ; Tissue Inhibitor of Metalloproteinase-2 - administration & dosage ; Tissue Inhibitor of Metalloproteinase-2 - metabolism ; Tropical environment ; Tropical environments ; Veterinary Science</subject><ispartof>PloS one, 2013-06, Vol.8 (6), p.e65083-e65083</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013. This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-f5d14f6d3c7a12129f886089ed4715c1ad2e4b3002ab83298db2312872e919bd3</citedby><cites>FETCH-LOGICAL-c692t-f5d14f6d3c7a12129f886089ed4715c1ad2e4b3002ab83298db2312872e919bd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1366366862/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1366366862?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23762288$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Moreira, Nei</contributor><creatorcontrib>Alvarez-Gallardo, Horacio</creatorcontrib><creatorcontrib>Kjelland, Michael E</creatorcontrib><creatorcontrib>Moreno, Juan F</creatorcontrib><creatorcontrib>Welsh, Jr, Thomas H</creatorcontrib><creatorcontrib>Randel, Ronald D</creatorcontrib><creatorcontrib>Lammoglia, Miguel A</creatorcontrib><creatorcontrib>Pérez-Martínez, Mario</creatorcontrib><creatorcontrib>Lara-Sagahón, Alma V</creatorcontrib><creatorcontrib>Esperón-Sumano, A Enrique</creatorcontrib><creatorcontrib>Romo, Salvador</creatorcontrib><title>Gamete therapeutics: recombinant protein adsorption by sperm for increasing fertility via artificial insemination</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>A decrease in fertility can have a negative economic impact, both locally and over a broader geographical scope, and this is especially the case with regard to the cattle industry. Therefore, much interest exists in evaluating proteins that might be able to increase the fertility of sperm. Heparin binding proteins (HBPs), specifically the fertility associated antigen (FAA) and the Type-2 tissue inhibitor of metalloproteinase (TIMP-2), act to favor the capacitation and acrosome reaction and perhaps even modulate the immune system's response toward the sperm. The objective of this research was to determine the effect on fertility of adding recombinant FAA (rFAA) and recombinant TIMP-2 (rTIMP-2) to bovine semen before cryopreservation for use in an artificial insemination (AI) program in a tropical environment. For this experiment, 100 crossbred (Bos taurus x Bos indicus) heifers were selected based on their estrus cycle, body condition score (BCS), of 4 to 6 on a scale of 1 to 9, and adequate anatomical conformation evaluated by pelvic and genital (normal) measurements. Heifers were synchronized using estradiol benzoate (EB), Celosil® (PGF2α) (Shering-Plough) and a controlled internal drug release (CIDR) device was inserted that contained progesterone. Inseminations were performed in two groups at random, 50 animals per group. The control group was inseminated with conventional semen. The treatment group was inseminated with semen containing rFAA (25 µg/mL) and rTIMP-2 (25 µg/mL). In the control group a 16% pregnancy rate was obtained versus a 40% pregnancy rate for the HBP treatment group, resulting in a significant difference (P = 0.0037). Given the results herein, one may conclude that the HBPs can increase fertility and could be an option for cattle in tropical conditions; however, one needs to consider the environment, nutrition, and the genetic interaction affecting the final result in whatever reproductive program that is implemented.</description><subject>17β-Estradiol</subject><subject>Acrosome reaction</subject><subject>Adsorption</subject><subject>Agriculture</subject><subject>Animals</subject><subject>Anticoagulants</subject><subject>Artificial insemination</subject><subject>Beef</subject><subject>Binding proteins</subject><subject>Biology</subject><subject>Bovidae</subject><subject>Capacitation</subject><subject>Cattle</subject><subject>Cryopreservation</subject><subject>Drug delivery systems</subject><subject>Economic impact</subject><subject>Estrus cycle</subject><subject>Estrus Synchronization</subject><subject>Female</subject><subject>Fertility</subject><subject>Fertility - physiology</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Heparin</subject><subject>Humans</subject><subject>Immune system</subject><subject>Impact analysis</subject><subject>Insemination, Artificial</subject><subject>Laboratory animals</subject><subject>Male</subject><subject>Males</subject><subject>Membrane Proteins - administration & dosage</subject><subject>Membrane Proteins - metabolism</subject><subject>Metalloproteinase</subject><subject>Nutrition</subject><subject>Ovulation</subject><subject>Plasma</subject><subject>Pregnancy</subject><subject>Pregnancy Rate</subject><subject>Progesterone</subject><subject>Prostate</subject><subject>Protein adsorption</subject><subject>Protein binding</subject><subject>Proteins</subject><subject>Recombinant proteins</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>Recombinant Proteins - metabolism</subject><subject>Reproduction (biology)</subject><subject>Semen</subject><subject>Semen - metabolism</subject><subject>Sex hormones</subject><subject>Sperm</subject><subject>Spermatozoa - metabolism</subject><subject>Tissue inhibitor of metalloproteinase 2</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - administration & dosage</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - metabolism</subject><subject>Tropical environment</subject><subject>Tropical environments</subject><subject>Veterinary 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therapeutics: recombinant protein adsorption by sperm for increasing fertility via artificial insemination</title><author>Alvarez-Gallardo, Horacio ; Kjelland, Michael E ; Moreno, Juan F ; Welsh, Jr, Thomas H ; Randel, Ronald D ; Lammoglia, Miguel A ; Pérez-Martínez, Mario ; Lara-Sagahón, Alma V ; Esperón-Sumano, A Enrique ; Romo, Salvador</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-f5d14f6d3c7a12129f886089ed4715c1ad2e4b3002ab83298db2312872e919bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>17β-Estradiol</topic><topic>Acrosome reaction</topic><topic>Adsorption</topic><topic>Agriculture</topic><topic>Animals</topic><topic>Anticoagulants</topic><topic>Artificial insemination</topic><topic>Beef</topic><topic>Binding 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alvarez-Gallardo, Horacio</au><au>Kjelland, Michael E</au><au>Moreno, Juan F</au><au>Welsh, Jr, Thomas H</au><au>Randel, Ronald D</au><au>Lammoglia, Miguel A</au><au>Pérez-Martínez, Mario</au><au>Lara-Sagahón, Alma V</au><au>Esperón-Sumano, A Enrique</au><au>Romo, Salvador</au><au>Moreira, Nei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gamete therapeutics: recombinant protein adsorption by sperm for increasing fertility via artificial insemination</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-06-10</date><risdate>2013</risdate><volume>8</volume><issue>6</issue><spage>e65083</spage><epage>e65083</epage><pages>e65083-e65083</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>A decrease in fertility can have a negative economic impact, both locally and over a broader geographical scope, and this is especially the case with regard to the cattle industry. Therefore, much interest exists in evaluating proteins that might be able to increase the fertility of sperm. Heparin binding proteins (HBPs), specifically the fertility associated antigen (FAA) and the Type-2 tissue inhibitor of metalloproteinase (TIMP-2), act to favor the capacitation and acrosome reaction and perhaps even modulate the immune system's response toward the sperm. The objective of this research was to determine the effect on fertility of adding recombinant FAA (rFAA) and recombinant TIMP-2 (rTIMP-2) to bovine semen before cryopreservation for use in an artificial insemination (AI) program in a tropical environment. For this experiment, 100 crossbred (Bos taurus x Bos indicus) heifers were selected based on their estrus cycle, body condition score (BCS), of 4 to 6 on a scale of 1 to 9, and adequate anatomical conformation evaluated by pelvic and genital (normal) measurements. Heifers were synchronized using estradiol benzoate (EB), Celosil® (PGF2α) (Shering-Plough) and a controlled internal drug release (CIDR) device was inserted that contained progesterone. Inseminations were performed in two groups at random, 50 animals per group. The control group was inseminated with conventional semen. The treatment group was inseminated with semen containing rFAA (25 µg/mL) and rTIMP-2 (25 µg/mL). In the control group a 16% pregnancy rate was obtained versus a 40% pregnancy rate for the HBP treatment group, resulting in a significant difference (P = 0.0037). Given the results herein, one may conclude that the HBPs can increase fertility and could be an option for cattle in tropical conditions; however, one needs to consider the environment, nutrition, and the genetic interaction affecting the final result in whatever reproductive program that is implemented.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23762288</pmid><doi>10.1371/journal.pone.0065083</doi><tpages>e65083</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2013-06, Vol.8 (6), p.e65083-e65083 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1366366862 |
source | PubMed Central(OpenAccess); Publicly Available Content (ProQuest) |
subjects | 17β-Estradiol Acrosome reaction Adsorption Agriculture Animals Anticoagulants Artificial insemination Beef Binding proteins Biology Bovidae Capacitation Cattle Cryopreservation Drug delivery systems Economic impact Estrus cycle Estrus Synchronization Female Fertility Fertility - physiology Fluorescent Antibody Technique, Indirect Heparin Humans Immune system Impact analysis Insemination, Artificial Laboratory animals Male Males Membrane Proteins - administration & dosage Membrane Proteins - metabolism Metalloproteinase Nutrition Ovulation Plasma Pregnancy Pregnancy Rate Progesterone Prostate Protein adsorption Protein binding Proteins Recombinant proteins Recombinant Proteins - administration & dosage Recombinant Proteins - metabolism Reproduction (biology) Semen Semen - metabolism Sex hormones Sperm Spermatozoa - metabolism Tissue inhibitor of metalloproteinase 2 Tissue Inhibitor of Metalloproteinase-2 - administration & dosage Tissue Inhibitor of Metalloproteinase-2 - metabolism Tropical environment Tropical environments Veterinary Science |
title | Gamete therapeutics: recombinant protein adsorption by sperm for increasing fertility via artificial insemination |
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