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Keller A, Kerns K. Sperm capacitation as a predictor of boar fertility. Mol Reprod Dev<\/i> 2023; 90: 594\u2013600.","DOI":"10.1002\/mrd.23690"},{"key":"2","unstructured":"2. Kemp B, Soede NM. Consequences of variation in interval from insemination to ovulation on fertilization in pigs. J Reprod Fertil Suppl<\/i> 1997; 52: 79\u201389."},{"key":"3","unstructured":"3. Soede NM, Kemp B. Expression of oestrus and timing of ovulation in pigs. J Reprod Fertil Suppl<\/i> 1997; 52: 91\u2013103."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Soede NM, Langendijk P, Kemp B. Reproductive cycles in pigs. Anim Reprod Sci<\/i> 2011; 124: 251\u2013258.","DOI":"10.1016\/j.anireprosci.2011.02.025"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5. Waberski D, Riesenbeck A, Schulze M, Weitze KF, Johnson L. Application of preserved boar semen for artificial insemination: Past, present and future challenges. Theriogenology<\/i> 2019; 137: 2\u20137.","DOI":"10.1016\/j.theriogenology.2019.05.030"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Rodriguez-Martinez H, Martinez-Serrano CA, Alvarez-Rodriguez M, Martinez EA, Roca J. Reproductive physiology of the boar: What defines the potential fertility of an ejaculate? Anim Reprod Sci<\/i> 2024; 269: 107476.","DOI":"10.1016\/j.anireprosci.2024.107476"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7. Llavanera M. Evaluation of sperm quality and male fertility: The use of molecular markers in boar sperm and seminal plasma. Anim Reprod Sci<\/i> 2024; 269: 107545.","DOI":"10.1016\/j.anireprosci.2024.107545"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Coy P, Garcia-Vazquez FA, Visconti PE, Aviles M. Roles of the oviduct in mammalian fertilization. Reproduction<\/i> 2012; 144: 649\u2013660.","DOI":"10.1530\/REP-12-0279"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Miller DJ. Sperm in the mammalian female reproductive tract: surfing through the tract to try to beat the odds. Annu Rev Anim Biosci<\/i> 2024; 12: 301\u2013319.","DOI":"10.1146\/annurev-animal-021022-040629"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Rodriguez-Martinez H, Saravia F, Wallgren M, Tienthai P, Johannisson A, Vazquez JM, Martinez E, Roca J, Sanz L, Calvete JJ. Boar spermatozoa in the oviduct. Theriogenology<\/i> 2005; 63: 514\u2013535.","DOI":"10.1016\/j.theriogenology.2004.09.028"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Hunter RH. Components of oviduct physiology in eutherian mammals. Biol Rev Camb Philos Soc<\/i> 2012; 287: 244\u2013255.","DOI":"10.1111\/j.1469-185X.2011.00196.x"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Hunter RH. Local action of progesterone leading to polyspermic fertilization in pigs. J Reprod Fertil<\/i> 1972; 31: 433\u2013444.","DOI":"10.1530\/jrf.0.0310433"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Hunter RH. Sperm transport and reservoirs in the pig oviduct in relation to the time of ovulation. J Reprod Fertil<\/i> 1981; 63: 109\u2013117.","DOI":"10.1530\/jrf.0.0630109"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. del Olmo D, Parrilla I, Sanchez-Osorio J, Gomis J, Angel MA, Tarantini T, Gil MA, Cuello C, Vazquez JL, Roca J, Vaquez JM, Martinez EA. Successful laparoscopic insemination with a very low number of flow cytometrically sorted boar sperm in field conditions. Theriogenology<\/i> 2014; 81: 315\u2013320.","DOI":"10.1016\/j.theriogenology.2013.09.031"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Mburu JN, Einarsson S, Lundeheim N, Rodriguez-Martinez H. Distribution, number and membrane integrity of spermatozoa in the pig oviduct in relation to spontaneous ovulation. Anim Reprod Sci<\/i> 1996; 45: 109\u2013121.","DOI":"10.1016\/S0378-4320(96)01566-7"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Mburu JN, Rodriguez-Martinez H, Einarsson S. Changes in sperm ultrastructure and localisation in the porcine oviduct around ovulation. Anim Reprod Sci<\/i> 1997; 47: 137\u2013148.","DOI":"10.1016\/S0378-4320(96)01631-4"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. La Spina FA, Puga Molina LC, Romarowski A, Vitale AM, Falzone TL, Krapf D, Hirohashi N, Buffone MG. Mouse sperm begin to undergo acrosomal exocytosis in the upper isthmus of the oviduct. Dev Biol<\/i> 2016; 411: 172\u2013182.","DOI":"10.1016\/j.ydbio.2016.02.006"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Ded L, Hwang JY, Miki K, Shi HF, Chung JJ. 3D in situ imaging of the female reproductive tract reveals molecular signatures of fertilizing spermatozoa in mice. eLife<\/i> 2020; 9.","DOI":"10.7554\/eLife.62043"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. Wang S, Larina IV. In vivo three-dimensional tracking of sperm behaviors in the mouse oviduct. Development<\/i> 2018; 145.","DOI":"10.1242\/dev.157685"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Chang H, Suarez SS. Unexpected flagellar movement patterns and epithelial binding behavior of mouse sperm in the oviduct. Biol Reprod<\/i> 2012; 86: 1\u20138.","DOI":"10.1095\/biolreprod.111.096578"},{"key":"21","doi-asserted-by":"crossref","unstructured":"21. Li S, Winuthayanon W. Oviduct: roles in fertilization and early embryo development. J Endocrinol<\/i> 2017; 232: R1\u2013R26.","DOI":"10.1530\/JOE-16-0302"},{"key":"22","doi-asserted-by":"crossref","unstructured":"22. Nosrati R, Driouchi A, Yip CM, Sinton D. Two-dimensional slither swimming of sperm within a micrometre of a surface. Nat Commun<\/i> 2015; 6: 8703.","DOI":"10.1038\/ncomms9703"},{"key":"23","doi-asserted-by":"crossref","unstructured":"23. Miller DJ. Sperm in the mammalian female reproductive tract: surfing through the tract to try to beat the odds. Annu Rev Anim Biosci<\/i> 2024; 12: 301\u2013319.","DOI":"10.1146\/annurev-animal-021022-040629"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Belda-Perez R, Cimini C, Valbonetti L, Orsini T, D\u2019Elia A, Massari R, Di Carlo C, Paradiso A, Maqsood S, Scavizzi F, Raspa M, Bernabo N, Barboni B. Exploring swine oviduct anatomy through micro-computed tomography: a 3D modeling perspective. Front Vet Sci<\/i> 2024; 11: 1456524.","DOI":"10.3389\/fvets.2024.1456524"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25. Hunter RH. Pre-ovulatory arrest and peri-ovulatory redistribution of competent spermatozoa in the isthmus of the pig oviduct. J Reprod Fertil<\/i> 1984; 72: 203\u2013211.","DOI":"10.1530\/jrf.0.0720203"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26. Wang S, Larina IV. In vivo dynamic 3D imaging of oocytes and embryos in the mouse oviduct. Cell Rep<\/i> 2021; 36: 109382.","DOI":"10.1016\/j.celrep.2021.109382"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27. Lee YL, Lee KF, Xu JS, Wang YL, Tsao SW, Yeung WS. Establishment and characterization of an immortalized human oviductal cell line. Mol Reprod Dev<\/i> 2001; 59: 400\u2013409.","DOI":"10.1002\/mrd.1046"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28. Miyashita N, Akagi S, Somfai T, Hirao Y. Serum-free spontaneously immortalized bovine oviduct epithelial cell conditioned medium promotes the early development of bovine in vitro fertilized embryos. J Reprod Dev<\/i> 2024; 70: 42\u201348.","DOI":"10.1262\/jrd.2023-031"},{"key":"29","doi-asserted-by":"crossref","unstructured":"29. Walter I. Culture of bovine oviduct epithelial cells (BOEC). Anat Rec<\/i> 1995; 243: 347\u2013356.","DOI":"10.1002\/ar.1092430309"},{"key":"30","doi-asserted-by":"crossref","unstructured":"30. Sostaric E, Dieleman SJ, van de Lest CH, Colenbrander B, Vos PL, Garcia-Gil N, Gadella BM. Sperm binding properties and secretory activity of the bovine oviduct immediately before and after ovulation. Mol Reprod Dev<\/i> 2008; 75: 60\u201374.","DOI":"10.1002\/mrd.20766"},{"key":"31","doi-asserted-by":"crossref","unstructured":"31. Schmaltz-Panneau B, Locatelli Y, Uzbekova S, Perreau C, Mermillod P. Bovine oviduct epithelial cells dedifferentiate partly in culture, while maintaining their ability to improve early embryo development rate and quality. Reprod Domest Anim<\/i> 2015; 50: 719\u2013729.","DOI":"10.1111\/rda.12556"},{"key":"32","doi-asserted-by":"crossref","unstructured":"32. Lamy J, Corbin E, Blache MC, Garanina AS, Uzbekov R, Mermillod P, Saint-Dizier M. Steroid hormones regulate sperm-oviduct interactions in the bovine. Reproduction<\/i> 2017; 154: 497\u2013508.","DOI":"10.1530\/REP-17-0328"},{"key":"33","doi-asserted-by":"crossref","unstructured":"33. Ellington JE, Evenson DP, Wright RW Jr, Jones AE, Schneider CS, Hiss GA, Brisbois RS. Higher-quality human sperm in a sample selectively attach to oviduct (fallopian tube) epithelial cells in vitro. Fertil Steril<\/i> 1999; 71: 924\u2013929.","DOI":"10.1016\/S0015-0282(99)00095-3"},{"key":"34","doi-asserted-by":"crossref","unstructured":"34. Chen S, Palma-Vera SE, Kempisty B, Rucinski M, Vernunft A, Schoen J. In vitro mimicking of estrous cycle stages: dissecting the impact of estradiol and progesterone on oviduct epithelium. Endocrinology<\/i> 2018; 159: 3421\u20133432.","DOI":"10.1210\/en.2018-00567"},{"key":"35","doi-asserted-by":"crossref","unstructured":"35. Suarez S, Redfern K, Raynor P, Martin F, Phillips DM. Attachment of boar sperm to mucosal explants of oviduct in vitro: possible role in formation of a sperm reservoir. Biol Reprod<\/i> 1991; 44: 998\u20131004.","DOI":"10.1095\/biolreprod44.6.998"},{"key":"36","doi-asserted-by":"crossref","unstructured":"36. Petrunkina AM, Gehlhaar R, Drommer W, Waberski D, Topfer-Petersen E. Selective sperm binding to pig oviductal epithelium in vitro. Reproduction<\/i> 2001; 121: 889\u2013896.","DOI":"10.1530\/rep.0.1210889"},{"key":"37","doi-asserted-by":"crossref","unstructured":"37. Mahe C, Laffont L, Pranomphon T, Schmaltz L, Reynaud K, Mermillod P, Saint-Dizier M. Assessment of sperm binding capacity in the reservoir using an in vitro model of oviduct epithelial spheroids in cattle. Methods Mol Biol<\/i> 2025; 2897: 687\u2013698.","DOI":"10.1007\/978-1-0716-4406-5_47"},{"key":"38","doi-asserted-by":"crossref","unstructured":"38. Schmaltz L, Prudhomme T, Tsikis G, Reynaud K, Merour I, Mermillod P, Saint-Dizier M. Sperm binding to oviduct epithelial spheroids varies among males and ejaculates but not among females in pigs. Theriogenology<\/i> 2024; 219: 116\u2013125.","DOI":"10.1016\/j.theriogenology.2024.02.022"},{"key":"39","doi-asserted-by":"crossref","unstructured":"39. Lawson EF, Ghosh A, Blanch V, Grupen CG, Aitken RJ, Lim R, Drury HR, Baker MA, Gibb Z, Tanwar PS. Establishment and characterization of oviductal organoids from farm and companion animalsdagger. Biol Reprod<\/i> 2023; 108: 854\u2013865.","DOI":"10.1093\/biolre\/ioad030"},{"key":"40","doi-asserted-by":"crossref","unstructured":"40. Gatimel N, Perez G, Bruno E, Sagnat D, Rolland C, Tanguy-Le-Gac Y, Di Donato E, Racaud C, Leandri R, Bettiol C, Deraison C, Motta JP, Huyghe E, Vergnolle N. Human fallopian tube organoids provide a favourable environment for sperm motility. Hum Reprod<\/i> 2025; 40: 503\u2013517.","DOI":"10.1093\/humrep\/deae258"},{"key":"41","doi-asserted-by":"crossref","unstructured":"41. Ford MJ, Harwalkar K, Pacis AS, Maunsell H, Wang YC, Badescu D, Teng K, Yamanaka N, Bouchard M, Ragoussis J, Yamanaka Y. Oviduct epithelial cells constitute two developmentally distinct lineages that are spatially separated along the distal-proximal axis. Cell Rep<\/i> 2021; 36: 109677.","DOI":"10.1016\/j.celrep.2021.109677"},{"key":"42","doi-asserted-by":"crossref","unstructured":"42. Bourdon G, Cadoret V, Charpigny G, Couturier-Tarrade A, Dalbies-Tran R, Flores MJ, Froment P, Raliou M, Reynaud K, Saint-Dizier M, Jouneau A. Progress and challenges in developing organoids in farm animal species for the study of reproduction and their applications to reproductive biotechnologies. Vet Res (Faisalabad)<\/i> 2021; 52: 42.","DOI":"10.1186\/s13567-020-00891-w"},{"key":"43","doi-asserted-by":"crossref","unstructured":"43. Kadirvel G, Machado SA, Korneli C, Collins E, Miller P, Bess KN, Aoki K, Tiemeyer M, Bovin N, Miller DJ. Porcine sperm bind to specific 6-sialylated biantennary glycans to form the oviduct reservoir. Biol Reprod<\/i> 2012; 87: 147.","DOI":"10.1095\/biolreprod.112.103879"},{"key":"44","doi-asserted-by":"crossref","unstructured":"44. Daigneault BW, McNamara KA, Purdy PH, Krisher RL, Knox RV, Rodriguez-Zas SL, Miller DJ. Enhanced fertility prediction of cryopreserved boar spermatozoa using novel sperm function assessment. Andrology<\/i> 2015; 3: 558\u2013568.","DOI":"10.1111\/andr.12035"},{"key":"45","doi-asserted-by":"crossref","unstructured":"45. Machado SA, Sharif M, Kadirvel G, Bovin N, Miller DJ. Adhesion to oviduct glycans regulates porcine sperm Ca2+ influx and viability. PLoS One<\/i> 2020; 15: e0237666.","DOI":"10.1371\/journal.pone.0237666"},{"key":"46","doi-asserted-by":"crossref","unstructured":"46. Soto-Heras S, Volz LJ, Bovin N, Miller DJ. Porcine sperm bind to an oviduct glycan coupled to glass surfaces as a model of sperm interaction with the oviduct. Sci Rep<\/i> 2025; 15: 4680.","DOI":"10.1038\/s41598-025-88986-2"},{"key":"47","doi-asserted-by":"crossref","unstructured":"47. Camara Pirez M, Steele H, Reese S, Kolle S. Bovine sperm-oviduct interactions are characterized by specific sperm behaviour, ultrastructure and tubal reactions which are impacted by sex sorting. Sci Rep<\/i> 2020; 10: 16522.","DOI":"10.1038\/s41598-020-73592-1"},{"key":"48","doi-asserted-by":"crossref","unstructured":"48. Miller DJ. Review: The epic journey of sperm through the female reproductive tract. Animal<\/i> 2018; 12: s110\u2013s120.","DOI":"10.1017\/S1751731118000526"},{"key":"49","doi-asserted-by":"crossref","unstructured":"49. Saint-Dizier M, Mahe C, Reynaud K, Tsikis G, Mermillod P, Druart X. Sperm interactions with the female reproductive tract: A key for successful fertilization in mammals. Mol Cell Endocrinol<\/i> 2020; 516: 110956.","DOI":"10.1016\/j.mce.2020.110956"},{"key":"50","doi-asserted-by":"crossref","unstructured":"50. Schmaltz L, Barakat E, Fleurot R, Uzbekov R, Reynaud K, Laffont L, Tsikis G, Merour I, Mermillod P, Saint-Dizier M. Phosphatidylserine on sperm head interact with Annexin A5 on oviduct luminal cilia to form a sperm reservoir in pigs. Eur J Cell Biol<\/i> 2024; 104: 151471.","DOI":"10.1016\/j.ejcb.2024.151471"},{"key":"51","doi-asserted-by":"crossref","unstructured":"51. Machado SA, Kadirvel G, Daigneault BW, Korneli C, Miller P, Bovin N, Miller DJ. LewisX-containing glycans on the porcine oviductal epithelium contribute to formation of the sperm reservoir. Biol Reprod<\/i> 2014; 91: 140.","DOI":"10.1095\/biolreprod.114.119503"},{"key":"52","doi-asserted-by":"crossref","unstructured":"52. Teijeiro JM, Ignotz GG, Marini PE. Annexin A2 is involved in pig (Sus scrofa)sperm-oviduct interaction. Mol Reprod Dev<\/i> 2009; 76: 334\u2013341.","DOI":"10.1002\/mrd.20958"},{"key":"53","doi-asserted-by":"crossref","unstructured":"53. Ignotz GG, Cho MY, Suarez SS. Annexins are candidate oviductal receptors for bovine sperm surface proteins and thus may serve to hold bovine sperm in the oviductal reservoir. Biol Reprod<\/i> 2007; 77: 906\u2013913.","DOI":"10.1095\/biolreprod.107.062505"},{"key":"54","doi-asserted-by":"crossref","unstructured":"54. Mahe C, Mowinska AM, Albrecht E, Reynaud K, Lavigne R, Com E, Pineau C, Mermillod P, Saint-Dizier M, Schoen J. Laser capture proteomics reveals new candidates for sperm-interacting proteins in the bovine oviduct epithelium. Reproduction<\/i> 2025; 170.","DOI":"10.1530\/REP-24-0390"},{"key":"55","doi-asserted-by":"crossref","unstructured":"55. Gwathmey TM, Ignotz GG, Mueller JL, Manjunath P, Suarez SS. Bovine seminal plasma proteins PDC-109, BSP-A3, and BSP-30-kDa share functional roles in storing sperm in the oviduct. Biol Reprod<\/i> 2006; 75: 501\u2013507.","DOI":"10.1095\/biolreprod.106.053306"},{"key":"56","doi-asserted-by":"crossref","unstructured":"56. Ekhlasi-Hundrieser M, Gohr K, Wagner A, Tsolova M, Petrunkina A, Topfer-Petersen E. Spermadhesin AQN1 is a candidate receptor molecule involved in the formation of the oviductal sperm reservoir in the pig. Biol Reprod<\/i> 2005; 73: 536\u2013545.","DOI":"10.1095\/biolreprod.105.040824"},{"key":"57","doi-asserted-by":"crossref","unstructured":"57. Suarez SS, Pacey AA. Sperm transport in the female reproductive tract. Hum Reprod Update<\/i> 2006; 12: 23\u201337.","DOI":"10.1093\/humupd\/dmi047"},{"key":"58","doi-asserted-by":"crossref","unstructured":"58. Puga Molina LC, Luque GM, Balestrini PA, Marin-Briggiler CI, Romarowski A, Buffone MG. Molecular basis of human sperm capacitation. Front Cell Dev Biol<\/i> 2018; 6: 72.","DOI":"10.3389\/fcell.2018.00072"},{"key":"59","doi-asserted-by":"crossref","unstructured":"59. Fazeli A, Duncan AE, Watson PF, Holt WV. Sperm-oviduct interaction: induction of capacitation and preferential binding of uncapacitated spermatozoa to oviductal epithelial cells in porcine species. Biol Reprod<\/i> 1999; 60: 879\u2013886.","DOI":"10.1095\/biolreprod60.4.879"},{"key":"60","doi-asserted-by":"crossref","unstructured":"60. Waberski D, Magnus F, Ardon F, Petrunkina AM, Weitze KF, Topfer-Petersen E. Binding of boar spermatozoa to oviductal epithelium in vitro in relation to sperm morphology and storage time. Reproduction<\/i> 2006; 131: 311\u2013318.","DOI":"10.1530\/rep.1.00814"},{"key":"61","doi-asserted-by":"crossref","unstructured":"61. Lefebvre R, Suarez SS. Effect of capacitation on bull sperm binding to homologous oviductal epithelium. Biol Reprod<\/i> 1996; 54: 575\u2013582.","DOI":"10.1095\/biolreprod54.3.575"},{"key":"62","unstructured":"62. Teijeiro JM, Munuce MJ, Caille AM, Zumoffen C, Marini PE. Use of annexin V based sperm selection in assisted reproduction. Andrology<\/i> 2017; 6: 1."},{"key":"63","doi-asserted-by":"crossref","unstructured":"63. Rival CM, Xu W, Shankman LS, Morioka S, Arandjelovic S, Lee CS, Wheeler KM, Smith RP, Haney LB, Isakson BE, Purcell S, Lysiak JJ, Ravichandran KS. Phosphatidylserine on viable sperm and phagocytic machinery in oocytes regulate mammalian fertilization. Nat Commun<\/i> 2019; 10: 4456.","DOI":"10.1038\/s41467-019-12406-z"},{"key":"64","doi-asserted-by":"crossref","unstructured":"64. Hughes JR, McMorrow KJ, Bovin N, Miller DJ. An oviduct glycan increases sperm lifespan by diminishing the production of ubiquinone and reactive oxygen species. Biol Reprod<\/i> 2023; 109: 356\u2013366.","DOI":"10.1093\/biolre\/ioad074"},{"key":"65","doi-asserted-by":"crossref","unstructured":"65. Lopez-Ubeda R, Garcia-Vazquez FA, Gadea J, Matas C. Oviductal epithelial cells selected boar sperm according to their functional characteristics. Asian J Androl<\/i> 2017; 19: 396\u2013403.","DOI":"10.4103\/1008-682X.173936"},{"key":"66","doi-asserted-by":"crossref","unstructured":"66. Petrunkina AM, Simon K, Gunzel-Apel AR, Topfer-Petersen E. Kinetics of protein tyrosine phosphorylation in sperm selected by binding to homologous and heterologous oviductal explants: how specific is the regulation by the oviduct? Theriogenology<\/i> 2004; 61: 1617\u20131634.","DOI":"10.1016\/j.theriogenology.2003.09.011"},{"key":"67","doi-asserted-by":"crossref","unstructured":"67. Leemans B, Gadella BM, Sostaric E, Nelis H, Stout TA, Hoogewijs M, Van Soom A. Oviduct binding and elevated environmental ph induce protein tyrosine phosphorylation in stallion spermatozoa. Biol Reprod<\/i> 2014; 91: 13.","DOI":"10.1095\/biolreprod.113.116418"},{"key":"68","doi-asserted-by":"crossref","unstructured":"68. Luno V, Lopez-Ubeda R, Garcia-Vazquez FA, Gil L, Matas C. Boar sperm tyrosine phosphorylation patterns in the presence of oviductal epithelial cells: in vitro, ex vivo, and in vivo models. Reproduction<\/i> 2013; 146: 315\u2013324.","DOI":"10.1530\/REP-13-0159"},{"key":"69","doi-asserted-by":"crossref","unstructured":"69. Hunter RH, Flechon B, Flechon JE. Pre- and peri-ovulatory distribution of viable spermatozoa in the pig oviduct: a scanning electron microscope study. Tissue Cell<\/i> 1987; 19: 423\u2013436.","DOI":"10.1016\/0040-8166(87)90037-1"},{"key":"70","doi-asserted-by":"crossref","unstructured":"70. Abe H, Hoshi H. Morphometric and ultrastructural changes in ciliated cells of the oviductal epithelium in prolific Chinese Meishan and Large White pigs during the oestrous cycle. Reprod Domest Anim<\/i> 2008; 43: 66\u201373.","DOI":"10.1111\/j.1439-0531.2007.00856.x"},{"key":"71","doi-asserted-by":"crossref","unstructured":"71. DeMott RP, Suarez SS. Hyperactivated sperm progress in the mouse oviduct. Biol Reprod<\/i> 1992; 46: 779\u2013785.","DOI":"10.1095\/biolreprod46.5.779"},{"key":"72","doi-asserted-by":"crossref","unstructured":"72. Donnellan EM, Lonergan P, Meade KG, Fair S. An ex-vivo assessment of differential sperm transport in the female reproductive tract between high and low fertility bulls. Theriogenology<\/i> 2022; 181: 42\u201349.","DOI":"10.1016\/j.theriogenology.2022.01.011"},{"key":"73","doi-asserted-by":"crossref","unstructured":"73. Nag P, Kumaresan A, Akshaya S, Manimaran A, Rajendran D, Paul N, Sharma A, Karuthadurai T, Kaustubh S, Jeyakumar S, Ramesha K. Sperm phenotypic characteristics and oviduct binding ability are altered in breeding bulls with high sperm DNA fragmentation index. Theriogenology<\/i> 2021; 172: 80\u201387.","DOI":"10.1016\/j.theriogenology.2021.06.006"},{"key":"74","doi-asserted-by":"crossref","unstructured":"74. De pauw I, Van Soom A, Laevens H, Verberckmoes S, de Kruif A. Sperm binding to epithelial oviduct explants in bulls with different nonreturn rates investigated with a new in vitro model. Biol Reprod<\/i> 2002; 67: 1073\u20131079.","DOI":"10.1095\/biolreprod67.4.1073"},{"key":"75","doi-asserted-by":"crossref","unstructured":"75. Saraf KK, Singh RK, Kumaresan A, Nayak S, Chhillar S, Lathika S, Datta TK, Mohanty TK. Sperm functional attributes and oviduct explant binding capacity differs between bulls with different fertility ratings in the water buffalo (Bubalus bubalis). Reprod Fertil Dev<\/i> 2019; 31: 395\u2013403.","DOI":"10.1071\/RD17452"},{"key":"76","doi-asserted-by":"crossref","unstructured":"76. Silva MA, Cortat PR, Consentini CEC, Pinto SCC, Celeghini ECC, Carvalho JO, Melo LF, Wiltbank M, Sartori R. Predicting sire fertility in artificial insemination of dairy cows by the ability of spermatozoa to bind to oviduct cell aggregates. J Dairy Sci<\/i> 2025; 108: 12722-12733.","DOI":"10.3168\/jds.2025-27057"},{"key":"77","doi-asserted-by":"crossref","unstructured":"77. Winters RA, Hamilton DN, Bhatnagar AS, Fitzgerald R, Bovin N, Miller DJ. Porcine sperm binding to oviduct cells and glycans as supplements to traditional laboratory semen analysis. J Anim Sci<\/i> 2018; 96: 5265\u20135275.","DOI":"10.1093\/jas\/sky372"},{"key":"78","doi-asserted-by":"crossref","unstructured":"78. Daigneault BW, McNamara KA, Purdy PH, Krisher RL, Knox RV, Miller DJ. Novel and traditional traits of frozen-thawed porcine sperm related to in vitro fertilization success. Theriogenology<\/i> 2014; 82: 266\u2013273.","DOI":"10.1016\/j.theriogenology.2014.04.006"},{"key":"79","doi-asserted-by":"crossref","unstructured":"79. Waberski D, Magnus F, Mendonca Ferreira F, Petrunkina AM, Weitze KF, Topfer-Petersen E. Importance of sperm-binding assays for fertility prognosis of porcine spermatozoa. Theriogenology<\/i> 2005; 63: 470\u2013484.","DOI":"10.1016\/j.theriogenology.2004.09.025"},{"key":"80","doi-asserted-by":"crossref","unstructured":"80. Alvarez-Rodriguez M, Atikuzzaman M, Venhoranta H, Wright D, Rodriguez-Martinez H. Expression of immune regulatory genes in the porcine internal genital tract is differentially triggered by spermatozoa and seminal plasma. Int J Mol Sci<\/i> 2019; 20.","DOI":"10.3390\/ijms20030513"},{"key":"81","doi-asserted-by":"crossref","unstructured":"81. Martinez CA, Alvarez-Rodriguez M, Wright D, Rodriguez-Martinez H. Does the pre-ovulatory pig oviduct rule sperm capacitation in vivo mediating transcriptomics of catsper channels? Int J Mol Sci<\/i> 2020; 21.","DOI":"10.3390\/ijms21051840"},{"key":"82","doi-asserted-by":"crossref","unstructured":"82. Alminana C, Caballero I, Heath PR, Maleki-Dizaji S, Parrilla I, Cuello C, Gil MA, Vazquez JL, Vazquez JM, Roca J, Martinez EA, Holt WV, Fazeli A. The battle of the sexes starts in the oviduct: modulation of oviductal transcriptome by X and Y-bearing spermatozoa. BMC Genomics<\/i> 2014; 15: 293.","DOI":"10.1186\/1471-2164-15-293"},{"key":"83","doi-asserted-by":"crossref","unstructured":"83. Lopez-Ubeda R, Garcia-Vazquez FA, Romar R, Gadea J, Munoz M, Hunter RH, Coy P. Oviductal transcriptome is modified after insemination during spontaneous ovulation in the sow. PLoS One<\/i> 2015; 10: e0130128.","DOI":"10.1371\/journal.pone.0130128"},{"key":"84","doi-asserted-by":"crossref","unstructured":"84. Georgiou AS, Snijders AP, Sostaric E, Aflatoonian R, Vazquez JL, Vazquez JM, Roca J, Martinez EA, Wright PC, Fazeli A. Modulation of the oviductal environment by gametes. J Proteome Res<\/i> 2007; 6: 4656\u20134666.","DOI":"10.1021\/pr070349m"},{"key":"85","doi-asserted-by":"crossref","unstructured":"85. Georgiou AS, Sostaric E, Wong CH, Snijders AP, Wright PC, Moore HD, Fazeli A. Gametes alter the oviductal secretory proteome. Mol Cell Proteomics<\/i> 2005; 4: 1785\u20131796.","DOI":"10.1074\/mcp.M500119-MCP200"},{"key":"86","doi-asserted-by":"crossref","unstructured":"86. Tom\u00e1nek M, Kope\u010dn\u00fd V, Ka\u0148ka J. Genome reactivaton in developing early pig embryos: an ultrastructural and autoradiographic analysis. Anat Embryol (Berl)<\/i> 1989; 180: 309\u2013316.","DOI":"10.1007\/BF00315889"},{"key":"87","doi-asserted-by":"crossref","unstructured":"87. Huang VW, Zhao W, Lee CL, Lee CY, Lam KK, Ko JK, Yeung WS, Ho PC, Chiu PC. Cell membrane proteins from oviductal epithelial cell line protect human spermatozoa from oxidative damage. Fertil Steril<\/i> 2013; 99: 1444\u20131452 e3.","DOI":"10.1016\/j.fertnstert.2012.11.056"},{"key":"88","doi-asserted-by":"crossref","unstructured":"88. Bureau M, Bailey JL, Sirard MA. Influence of oviductal cells and conditioned medium on porcine gametes. Zygote<\/i> 2000; 8: 139\u2013144.","DOI":"10.1017\/S0967199400000915"},{"key":"89","doi-asserted-by":"crossref","unstructured":"89. Gualtieri R, Talevi R. Selection of highly fertilization-competent bovine spermatozoa through adhesion to the Fallopian tube epithelium in vitro. Reproduction<\/i> 2003; 125: 251\u2013258.","DOI":"10.1530\/rep.0.1250251"},{"key":"90","doi-asserted-by":"crossref","unstructured":"90. Kon Y, Iwata H, Shiono H, Matsubara K, Kurita A, Sakaguchi Y, Kuwayama T, Monji Y. Effect of carbohydrates on the ability of bull sperm to bind to bovine oviduct epithelial cells. Reprod Domest Anim<\/i> 2009; 44: 365\u2013370.","DOI":"10.1111\/j.1439-0531.2007.01013.x"},{"key":"91","doi-asserted-by":"crossref","unstructured":"91. El-Sokary MMM, Shehata SF, Mahmoud KGM. Heparin and Progesterone Exert Synergistic Effects to Improve the In-Vitro Fertilization Rate of Bovine Sperm Bound to Oviduct Cell Aggregates from the Isthmus. Vet Sci<\/i> 2022; 9.","DOI":"10.3390\/vetsci9070372"}],"container-title":["Journal of Reproduction and Development"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jrd\/72\/3\/72_2025-112\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,6,20]],"date-time":"2026-06-20T03:22:31Z","timestamp":1781925751000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/jrd\/72\/3\/72_2025-112\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026]]},"references-count":91,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2026]]}},"URL":"https:\/\/doi.org\/10.1262\/jrd.2025-112","relation":{},"ISSN":["0916-8818","1348-4400"],"issn-type":[{"value":"0916-8818","type":"print"},{"value":"1348-4400","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026]]},"article-number":"2025-112"}}