Ontology groups representing angiogenesis and blood vessels development are highly up-regulated during porcine oviductal epithelial cells long-term real-time proliferation – a primary cell culture approach

1. Huang DW, Sherman BT, Tan Q, Kir J, Liu D, Bryant D, Guo Y, Stephens R, Baseler MW, Lane HC, Lempicki RA. DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists. Nucleic Acids Res. 2007;35:W169-75; DOI:10.1093/nar/gkm415.10.1093/nar/gkm415193316917576678Search in Google Scholar

2. Walter W, Sánchez-Cabo F, Ricote M. GOplot: An R package for visually combining expression data with functional analysis. Bioinformatics. 2015;31:2912–4; DOI:10.1093/bioinformatics/btv300.10.1093/bioinformatics/btv30025964631Search in Google Scholar

3. von Mering C, Jensen LJ, Snel B, Hooper SD, Krupp M, Foglierini M, Jouffre N, Huynen MA, Bork P. STRING: known and predicted protein-protein associations, integrated and transferred across organisms. Nucleic Acids Res. 2004;33:D433–7; DOI:10.1093/nar/gki005.10.1093/nar/gki00553995915608232Search in Google Scholar

4. Besenfelder U, Havlicek V, Brem G. Role of the Oviduct in Early Embryo Development. Reprod Domest Anim. 2012;47:156–63; DOI:10.1111/j.1439-0531.2012.02070.x.10.1111/j.1439-0531.2012.02070.x22827365Search in Google Scholar

5. Avilés M, Gutiérrez-Adán A, Coy P. Oviductal secretions: will they be key factors for the future ARTs? MHR Basic Sci Reprod Med. 2010;16:896–906; DOI:10.1093/molehr/gaq056.10.1093/molehr/gaq05620584881Search in Google Scholar

6. Leese HJ, Hugentobler SA, Gray SM, Morris DG, Sturmey RG, Whitear S-L, Sreenan JM. Female reproductive tract fluids: composition, mechanism of formation and potential role in the developmental origins of health and disease. Reprod Fertil Dev. 2008;20:1–8.10.1071/RD0715318154692Search in Google Scholar

7. Zumoffen CM, Gil R, Caille AM, Morente C, Munuce MJ, Ghersevich SA. A protein isolated from human oviductal tissue in vitro secretion, identified as human lactoferrin, interacts with spermatozoa and oocytes and modulates gamete interaction. Hum Reprod. 2013;28:1297–308; DOI:10.1093/humrep/det016.10.1093/humrep/det01623427237Search in Google Scholar

8. Nawrocki MJ, Budna J, Celichowski P, Khozmi R, Bryja A, Kranc W, Borys S, Ciesiółka S, Knap S, Jeseta M, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. Analysis of fructose and mannose regulatory peptides signaling pathway in porcine epithelial oviductal cells (OECs) primary cultured long-term in vitro. Adv Cell Biol. 2017;5:129–35; DOI:10.1515/acb-2017-0011.10.1515/acb-2017-0011Search in Google Scholar

9. Kranc W, Jankowski M, Budna J, Celichowski P, Khozmi R, Bryja A, Borys S, Dyszkiewicz-Konwińska M, Jeseta M, Magas M, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. Amino acids metabolism and degradation is regulated during porcine oviductal epithelial cells (OECs) primary culture in vitro a signaling pathways activation approach. Med J Cell Biol. 2018;6:18–26; DOI:10.2478/acb-2018-0004.10.2478/acb-2018-0004Search in Google Scholar

10. Ferrara N. Vascular Endothelial Growth Factor: Basic Science and Clinical Progress. Endocr Rev. 2004;25:581–611; DOI:10.1210/er.2003-0027.10.1210/er.2003-002715294883Search in Google Scholar

11. Ribeiro LA, Bacci ML, Seren E, Tamanini C, Forni M. Characterization and differential expression of vascular endothelial growth factor isoforms and receptors in swine corpus luteum throughout estrous cycle. Mol Reprod Dev. 2007;74:163–71; DOI:10.1002/mrd.20589.10.1002/mrd.2058916967516Search in Google Scholar

12. Sugino N, Kashida S, Takiguchi S, Karube A, Kato H. Expression of Vascular Endothelial Growth Factor and Its Receptors in the Human Corpus Luteum during the Menstrual Cycle and in Early Pregnancy ¹. J Clin Endocrinol Metab. 2000;85:3919–24; DOI:10.1210/jcem.85.10.6888.10.1210/jcem.85.10.688811061557Search in Google Scholar

13. Goodger AM, Rogers PA. Endometrial endothelial cell proliferation during the menstrual cycle. Hum Reprod. 1994;9:399–405.10.1093/oxfordjournals.humrep.a1385167516347Search in Google Scholar

14. Reynolds LP, Redmer DA. Angiogenesis in the placenta. Biol Reprod. 2001;64:1033–40.10.1095/biolreprod64.4.103311259247Search in Google Scholar

15. Nawrocki MJ, Celichowski P, Budna J, Bryja A, Kranc W, Ciesiółka S, Borys S, Knap S, Jeseta M, Khozmi R, Bukowska D, Antosik P, Brüssow KP, Bruska M, Nowicki M, Zabel M, Kempisty B. The blood vessels development, morphogenesis and blood circulation are three ontologic groups highly up-regulated in porcine oocytes before in vitro maturation. Adv Cell Biol. 2017;5:135–42; DOI:10.1515/acb-2017-0012.10.1515/acb-2017-0012Search in Google Scholar

16. Lam PM, Briton-Jones C, Cheung CK, Lok IH, Cheung LP, Haines C. In vivo regulation of mRNA expression of vascular endothelial growth factor receptors (KDR and flt-1) in the human oviduct. Fertil Steril. 2004;81:416–23; DOI:10.1016/j.fertnstert.2003.06.025.10.1016/j.fertnstert.2003.06.02514967383Search in Google Scholar

17. Małysz-Cymborska I, Andronowska A. Expression of the vascular endothelial growth factor receptor system in porcine oviducts after induction of ovulation and superovulation. Domest Anim Endocrinol. 2014;49:86–95; DOI:10.1016/J.DOMANIEND.2014.06.003.10.1016/j.domaniend.2014.06.00325124278Search in Google Scholar

18. López Albors O, Olsson F, Llinares AB, Gutiérrez H, Latorre R, Candanosa E, Guillén-Martínez A, Izquierdo-Rico MJ. Expression of the vascular endothelial growth factor system (VEGF) in the porcine oviduct during the estrous cycle. Theriogenology. 2017;93:46–54.10.1016/j.theriogenology.2017.01.02828257866Search in Google Scholar

19. Nelis H, D’Herde K, Goossens K, Vandenberghe L, Leemans B, Forier K, Smits K, Braeckmans K, Peelman L, Van Soom A. Equine oviduct explant culture: a basic model to decipher embryo maternal communication. Reprod Fertil Dev. 2014;26:954–66; DOI:10.1071/RD13089.10.1071/RD1308923902648Search in Google Scholar

20. Lanahan A, Zhang X, Fantin A, Zhuang Z, Rivera-Molina F, Speichinger K, Prahst C, Zhang J, Wang Y, Davis G, Toomre D, Ruhrberg C, Simons M. The Neuropilin 1 Cytoplasmic Domain Is Required for VEGF-A-Dependent Arteriogenesis. Dev Cell. 2013;25:156–68; DOI:10.1016/J.DEVCEL.2013.03.019.10.1016/j.devcel.2013.03.019377415423639442Search in Google Scholar

21. Xu X, Yang X-Y, He B-W, Yang W-J, Cheng W-W. Placental NRP1 and VEGF expression in pre-eclamptic women and in a homocysteine-treated mouse model of pre-eclampsia. Eur J Obstet Gynecol Reprod Biol. 2016;196:69–75; DOI:10.1016/j.ejogrb.2015.11.017.10.1016/j.ejogrb.2015.11.01726708340Search in Google Scholar

22. Szpera-Gozdziewicz A, Breborowicz GH. Endothelial dysfunction in the pathogenesis of pre-eclampsia. Front Biosci (Landmark Ed.). 2014;19:734–46.10.2741/4240Search in Google Scholar

23. Akbar F, Heinonen S, Pirskanen M, Uimari P, Tuomainen T-P, Salonen JT. Haplotypic association of DDAH1 with susceptibility to pre-eclampsia. MHR Basic Sci Reprod Med. 2005;11:73–7; DOI:10.1093/molehr/gah116.10.1093/molehr/gah11615501905Search in Google Scholar

24. Murray-Rust J, Leiper J, McAlister M, Phelan J, Tilley S, Maria JS, Vallance P, McDonald N. Structural insights into the hydrolysis of cellular nitric oxide synthase inhibitors by dimethylarginine dimethylaminohydrolase. Nat Struct Biol. 2001;8:679–83; DOI:10.1038/90387.10.1038/9038711473257Search in Google Scholar

25. Depoix CL, Flabat O, Debiève F, Hubinont C. HIF1A and EPAS1 mRNA and protein expression during in vitro culture of human primary term cytotrophoblasts and effect of oxygen tension on their expression. Reprod Biol. 2016;16:203–11; DOI:10.1016/j.repbio.2016.05.001.10.1016/j.repbio.2016.05.00127692362Search in Google Scholar

26. Dickson BJ, Gilestro GF. Regulation of Commissural Axon Pathfinding by Slit and its Robo Receptors. Annu Rev Cell Dev Biol. 2006;22:651–75; DOI:10.1146/annurev.cellbio.21.090704.151234.10.1146/annurev.cellbio.21.090704.15123417029581Search in Google Scholar

27. Zhou W-J, Geng ZH, Chi S, Zhang W, Niu X-F, Lan S-J, Ma L, Yang X, Wang L-J, Ding Y-Q, Geng J-G. Slit-Robo signaling induces malignant transformation through Hakai-mediated E-cadherin degradation during colorectal epithelial cell carcinogenesis. Cell Res. 2011;21:609–26; DOI:10.1038/cr.2011.17.10.1038/cr.2011.17320365421283129Search in Google Scholar

28. Narayan G, Goparaju C, Arias-Pulido H, Kaufmann AM, Schneider A, Dürst M, Mansukhani M, Pothuri B, Murty V V. Promoter hypermethylation-mediated inactivation of multiple Slit-Robo pathway genes in cervical cancer progression. Mol Cancer. 2006;5:16; DOI:10.1186/1476-4598-5-16.10.1186/1476-4598-5-16148271416700909Search in Google Scholar

29. Yuasa-Kawada J, Kinoshita-Kawada M, Rao Y, Wu JY. Deubiquitinating enzyme USP33/VDU1 is required for Slit signaling in inhibiting breast cancer cell migration. Proc Natl Acad Sci. 2009;106:14530–5; DOI:10.1073/pnas.0801262106.10.1073/pnas.0801262106273286019706539Search in Google Scholar

30. Duncan WC, McDonald SE, Dickinson RE, Shaw JL V, Lourenco PC, Wheelhouse N, Lee K-F, Critchley HOD, Horne AW. Expression of the repulsive SLIT/ROBO pathway in the human endometrium and Fallopian tube. Mol Hum Reprod. 2010;16:950–9; DOI:10.1093/molehr/gaq055.10.1093/molehr/gaq055299205020651036Search in Google Scholar

31. Li P, Peng H, Lu W, Shuai H, Zha Q, Yeung C, Li H, Wang L, Ho Lee KK, Zhu W, Yang X. Role of Slit2/Robo1 in trophoblast invasion and vascular remodeling during ectopic tubal pregnancy. Placenta. 2015;36:1087–94; DOI:10.1016/j.placenta.2015.08.002.10.1016/j.placenta.2015.08.00226282852Search in Google Scholar

32. Masaki T. Historical review: Endothelin. Trends Pharmacol Sci. 2004;25:219–24; DOI:10.1016/j.tips.2004.02.008.10.1016/j.tips.2004.02.00815063086Search in Google Scholar

33. Bridges PJ, Cho J, Ko C. Endothelins in regulating ovarian and oviductal function. Front Biosci (Schol Ed). 2011;3:145–55.10.2741/s140Search in Google Scholar

34. Yamamoto Y, Kohka M, Kobayashi Y, Woclawek-Potocka I, Okuda K. Endothelin as a local regulating factor in the bovine oviduct. Reprod Fertil Dev. 2016;28:673; DOI:10.1071/RD14076.10.1071/RD1407625370848Search in Google Scholar

35. Kobayashi Y, Yoshimoto Y, Yamamoto Y, Kimura K, Okuda K. Roles of EDNs in regulating oviductal NO synthesis and smooth muscle motility in cows. Reproduction. 2016;151:615–22; DOI:10.1530/REP-15-0586.10.1530/REP-15-058626980806Search in Google Scholar

36. Jeoung M, Lee S, Hawng H-K, Cheon Y-P, Jeong YK, Gye MC, Iglarz M, Ko C, Bridges PJ. Identification of a novel role for endothelins within the oviduct. Endocrinology. 2010;151:2858–67; DOI:10.1210/en.2009-1155.10.1210/en.2009-1155287581120357223Search in Google Scholar