Melatonin improves the maturation and developmental ability of bovine oocytes by up-regulating GJA4 to enhance gap junction intercellular communication

References

Acuña-Hernández, DG, Arreola-Mendoza, L, Santacruz-Márquez, R, García-Zepeda, SP, Parra-Forero, LY, Olivares-Reyes, JA, and Hernández-Ochoa, I (2018). Bisphenol A alters oocyte maturation by prematurely closing gap junctions in the cumulus cell–oocyte complex. Toxicology and Applied Pharmacology 344, 13–22.
| Bisphenol A alters oocyte maturation by prematurely closing gap junctions in the cumulus cell–oocyte complex.Crossref | GoogleScholarGoogle Scholar | 29458137PubMed |

An, Q, Peng, W, Cheng, Y, Lu, Z, Zhou, C, Zhang, Y, and Su, J (2019). Melatonin supplementation during in vitro maturation of oocyte enhances subsequent development of bovine cloned embryos. Journal of Cellular Physiology 234, 17370–17381.
| Melatonin supplementation during in vitro maturation of oocyte enhances subsequent development of bovine cloned embryos.Crossref | GoogleScholarGoogle Scholar | 30786018PubMed |

Bagg, MA, Nottle, MB, Armstrong, DT, and Grupen, CG (2009). Effect of follicle size and dibutyryl cAMP on the cAMP content and gap junctional communication of porcine prepubertal cumulus–oocyte complexes during IVM. Reproduction, Fertility and Development 21, 796–804.
| Effect of follicle size and dibutyryl cAMP on the cAMP content and gap junctional communication of porcine prepubertal cumulus–oocyte complexes during IVM.Crossref | GoogleScholarGoogle Scholar |

Barceló-Fimbres, M, and Seidel, GE (2007). Effects of fetal calf serum, phenazine ethosulfate and either glucose or fructose during in vitro culture of bovine embryos on embryonic development after cryopreservation. Molecular Reproduction Development 74, 1395–1405.
| Effects of fetal calf serum, phenazine ethosulfate and either glucose or fructose during in vitro culture of bovine embryos on embryonic development after cryopreservation.Crossref | GoogleScholarGoogle Scholar | 17342731PubMed |

Barros, VRP, Monte, APO, Santos, JMS, Lins, TLBG, Cavalcante, AYP, Gouveia, BB, Müller, MC, Oliveira, JL, Donfack, NJ, Araújo, VR, and Matos, MHT (2020). Melatonin improves development, mitochondrial function and promotes the meiotic resumption of sheep oocytes from in vitro grown secondary follicles. Theriogenology 144, 67–73.
| Melatonin improves development, mitochondrial function and promotes the meiotic resumption of sheep oocytes from in vitro grown secondary follicles.Crossref | GoogleScholarGoogle Scholar | 31918071PubMed |

Bernal-Ulloa, SM, Lucas-Hahn, A, Herrmann, D, Hadeler, KG, Aldag, P, Baulain, U, and Niemann, H (2016). Oocyte pre-IVM with caffeine improves bovine embryo survival after vitrification. Theriogenology 86, 1222–1230.
| Oocyte pre-IVM with caffeine improves bovine embryo survival after vitrification.Crossref | GoogleScholarGoogle Scholar | 27180328PubMed |

Blackman, CF, Andrews, PW, Ubeda, A, Wang, X, House, DE, Trillo, MA, and Pimentel, ME (2001). Physiological levels of melatonin enhance gap junction communication in primary cultures of mouse hepatocytes. Cell Biology and Toxicology 17, 1–9.
| Physiological levels of melatonin enhance gap junction communication in primary cultures of mouse hepatocytes.Crossref | GoogleScholarGoogle Scholar | 11504445PubMed |

Brackett, BG, and Oliphant, G (1975). Capacitation of rabbit spermatozoa in vitro. Biology of Reproduction 12, 260–274.
| Capacitation of rabbit spermatozoa in vitro.Crossref | GoogleScholarGoogle Scholar | 1122333PubMed |

Campen, KA, Abbott, CR, Rispoli, LA, Payton, RR, Saxton, AM, and Edwards, JL (2018). Heat stress impairs gap junction communication and cumulus function of bovine oocytes. Journal of Reproduction and Development 64, 385–392.
| Heat stress impairs gap junction communication and cumulus function of bovine oocytes.Crossref | GoogleScholarGoogle Scholar |

Carabatsos, MJ, Sellitto, C, Goodenough, DA, and Albertini, DF (2000). Oocyte–granulosa cell heterologous gap junctions are required for the coordination of nuclear and cytoplasmic meiotic competence. Developmental Biology 226, 167–179.
| Oocyte–granulosa cell heterologous gap junctions are required for the coordination of nuclear and cytoplasmic meiotic competence.Crossref | GoogleScholarGoogle Scholar | 11023678PubMed |

Casillas, F, Ducolomb, Y, López, A, and Betancourt, M (2020). Effect of porcine immature oocyte vitrification on oocyte–cumulus cell gap junctional intercellular communication. Porcine Health Management 6, 37.
| Effect of porcine immature oocyte vitrification on oocyte–cumulus cell gap junctional intercellular communication.Crossref | GoogleScholarGoogle Scholar | 33292603PubMed |

Cavallari, FC, Leal, CLV, Zvi, R, and Hansen, PJ (2019). Effects of melatonin on production of reactive oxygen species and developmental competence of bovine oocytes exposed to heat shock and oxidative stress during in vitro maturation. Zygote 27, 180–186.
| Effects of melatonin on production of reactive oxygen species and developmental competence of bovine oocytes exposed to heat shock and oxidative stress during in vitro maturation.Crossref | GoogleScholarGoogle Scholar | 31171044PubMed |

Chang, AS, Dale, AN, and Moley, KH (2005). Maternal diabetes adversely affects preovulatory oocyte maturation, development, and granulosa cell apoptosis. Endocrinology 146, 2445–2453.
| Maternal diabetes adversely affects preovulatory oocyte maturation, development, and granulosa cell apoptosis.Crossref | GoogleScholarGoogle Scholar | 15718275PubMed |

Chang, HM, Cheng, JC, Taylor, E, and Leung, PC (2014). Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication activity in immortalized human granulosa cells. Molecular Human Reproduction 20, 373–383.
| Oocyte-derived BMP15 but not GDF9 down-regulates connexin43 expression and decreases gap junction intercellular communication activity in immortalized human granulosa cells.Crossref | GoogleScholarGoogle Scholar | 24413384PubMed |

Chen, YC, Chang, HM, Cheng, JC, Tsai, HD, Wu, CH, and Leung, PCK (2015). Transforming growth factor-β1 up-regulates connexin43 expression in human granulosa cells. Human Reproduction 30, 2190–2201.
| Transforming growth factor-β1 up-regulates connexin43 expression in human granulosa cells.Crossref | GoogleScholarGoogle Scholar | 26202915PubMed |

Clarke, HJ (2018). Regulation of germ cell development by intercellular signaling in the mammalian ovarian follicle. Wiley Interdisciplinary Reviews Developmental Biology 7, e294.
| Regulation of germ cell development by intercellular signaling in the mammalian ovarian follicle.Crossref | GoogleScholarGoogle Scholar |

Combelles, CMH, Gupta, S, and Agarwal, A (2009). Could oxidative stress influence the in-vitro maturation of oocytes? Reproductive BioMedicine Online 18, 864–880.
| Could oxidative stress influence the in-vitro maturation of oocytes?Crossref | GoogleScholarGoogle Scholar |

Cos, S, and Fernández, R (2000). Melatonin effects on intercellular junctional communication in MCF-7 human breast cancer cells. Journal of Pineal Research 29, 166–171.
| Melatonin effects on intercellular junctional communication in MCF-7 human breast cancer cells.Crossref | GoogleScholarGoogle Scholar | 11034114PubMed |

Cronier, L, Frendo, JL, Defamie, N, Pidoux, G, Bertin, G, Guibourdenche, J, Pointis, G, and Malassine, A (2003). Requirement of gap junctional intercellular communication for human villous trophoblast differentiation. Biology of Reproduction 69, 1472–1480.
| Requirement of gap junctional intercellular communication for human villous trophoblast differentiation.Crossref | GoogleScholarGoogle Scholar | 12826585PubMed |

De Los Reyes, M, Palomino, J, Gallegos, C, Espinoza, R, Dettleff, P, Peralta, OA, Parraguez, VH, and Ramirez, G (2020). Gene and protein expression of connexins 37 and 43 in cumulus–oocytes complexes throughout the canine oestrous cycle. Reproduction, Fertility and Development 32, 976–987.
| Gene and protein expression of connexins 37 and 43 in cumulus–oocytes complexes throughout the canine oestrous cycle.Crossref | GoogleScholarGoogle Scholar |

Ding, L, Zhang, F, Zhao, MX, Ren, XS, Chen, Q, Li, YH, Kang, YM, and Zhu, GQ (2016). Reduced lipolysis response to adipose afferent reflex involved in impaired activation of adrenoceptor-cAMP-PKA-hormone sensitive lipase pathway in obesity. Scientific Reports 6, 34374.
| Reduced lipolysis response to adipose afferent reflex involved in impaired activation of adrenoceptor-cAMP-PKA-hormone sensitive lipase pathway in obesity.Crossref | GoogleScholarGoogle Scholar | 27694818PubMed |

Domínguez, A, Salazar, Z, Betancourt, M, Ducolomb, Y, Casas, E, Fernández, F, Bahena, I, Salomón, A, Teteltitla, M, Martínez, R, Chaparro, A, Cuapio, P, Salazar-López, C, and Bonilla, E (2019). Effect of perfluorodecanoic acid on pig oocyte viability, intracellular calcium levels and gap junction intercellular communication during oocyte maturation in vitro. Toxicology In Vitro 58, 224–229.
| Effect of perfluorodecanoic acid on pig oocyte viability, intracellular calcium levels and gap junction intercellular communication during oocyte maturation in vitro.Crossref | GoogleScholarGoogle Scholar | 30946969PubMed |

Ezoe, K, Yabuuchi, A, Tani, T, Mori, C, Miki, T, Takayama, Y, Beyhan, Z, Kato, Y, Okuno, T, Kobayashi, T, and Kato, K (2015). Developmental competence of vitrified-warmed bovine oocytes at the germinal-vesicle stage is improved by cyclic adenosine monophosphate modulators during in vitro maturation. PLoS One 10, e0126801.
| Developmental competence of vitrified-warmed bovine oocytes at the germinal-vesicle stage is improved by cyclic adenosine monophosphate modulators during in vitro maturation.Crossref | GoogleScholarGoogle Scholar | 25965267PubMed |

Frielle, T, Daniel, KW, Caron, MG, and Lefkowitz, RJ (1988). Structural basis of beta-adrenergic receptor subtype specificity studied with chimeric beta 1/beta 2-adrenergic receptors. Proceedings of the National Academy of Sciences of the United States of America 85, 9494–9498.
| Structural basis of beta-adrenergic receptor subtype specificity studied with chimeric beta 1/beta 2-adrenergic receptors.Crossref | GoogleScholarGoogle Scholar | 2849109PubMed |

Gershon, E, Plaks, V, and Dekel, N (2008). Gap junctions in the ovary: expression, localization and function. Molecular and Cellular Endocrinology 282, 18–25.
| Gap junctions in the ovary: expression, localization and function.Crossref | GoogleScholarGoogle Scholar | 18162286PubMed |

Gilchrist, RB, Lane, M, and Thompson, JG (2008). Oocyte-secreted factors: regulators of cumulus cell function and oocyte quality. Human Reproduction Update 14, 159–177.
| Oocyte-secreted factors: regulators of cumulus cell function and oocyte quality.Crossref | GoogleScholarGoogle Scholar | 18175787PubMed |

Htet, M, Nally, JE, Shaw, A, Foote, BE, Martin, PE, and Dempsie, Y (2018). Connexin 43 plays a role in pulmonary vascular reactivity in mice. International Journal of Molecular Sciences 19, 1891.
| Connexin 43 plays a role in pulmonary vascular reactivity in mice.Crossref | GoogleScholarGoogle Scholar |

Kang, JT, Koo, OJ, Kwon, DK, Park, HJ, Jang, G, Kang, SK, and Lee, BC (2009). Effects of melatonin on in vitro maturation of porcine oocyte and expression of melatonin receptor RNA in cumulus and granulosa cells. Journal of Pineal Research 46, 22–28.
| Effects of melatonin on in vitro maturation of porcine oocyte and expression of melatonin receptor RNA in cumulus and granulosa cells.Crossref | GoogleScholarGoogle Scholar | 18494781PubMed |

Keshavarzi, S, Salehi, M, Farifteh-Nobijari, F, Hosseini, T, Hosseini, S, Ghazifard, A, Ghaffari Novin, M, Fallah-Omrani, V, Nourozian, M, and Hosseini, A (2018). Melatonin modifies histone acetylation during in vitro maturation of mouse oocytes. Cell Journal 20, 244–249.
| Melatonin modifies histone acetylation during in vitro maturation of mouse oocytes.Crossref | GoogleScholarGoogle Scholar | 29633602PubMed |

Lee, HJ, Lee, HJ, Sohn, EJ, Lee, EO, Kim, JH, Lee, MH, and Kim, SH (2012). Inhibition of connexin 26/43 and extracellular-regulated kinase protein plays a critical role in melatonin facilitated gap junctional intercellular communication in hydrogen peroxide-treated HaCaT keratinocyte cells. Evidence-Based Complementary and Alternative Medicine 2012, 589365.
| Inhibition of connexin 26/43 and extracellular-regulated kinase protein plays a critical role in melatonin facilitated gap junctional intercellular communication in hydrogen peroxide-treated HaCaT keratinocyte cells.Crossref | GoogleScholarGoogle Scholar | 23243457PubMed |

Lee, JY, Song, H, Dash, O, Park, M, Shin, NE, McLane, MW, Lei, J, Hwang, JY, and Burd, I (2019). Administration of melatonin for prevention of preterm birth and fetal brain injury associated with premature birth in a mouse model. The American Journal of Reproductive Immunology 82, e13151.
| Administration of melatonin for prevention of preterm birth and fetal brain injury associated with premature birth in a mouse model.Crossref | GoogleScholarGoogle Scholar | 31131935PubMed |

Leite, RF, Annes, K, Ispada, J, de Lima, CB, Dos Santos, ÉC, Fontes, PK, Nogueira, MFG, and Milazzotto, MP (2017). Oxidative stress alters the profile of transcription factors related to early development on in vitro produced embryos. Oxidative Medicine and Cellular Longevity 2017, 1502489.
| Oxidative stress alters the profile of transcription factors related to early development on in vitro produced embryos.Crossref | GoogleScholarGoogle Scholar | 29209446PubMed |

Li, R, Yu, C, Li, Y, Lam, TW, Yiu, SM, Kristiansen, K, and Wang, J (2009). SOAP2: an improved ultrafast tool for short read alignment. Bioinformatics 25, 1966–1967.
| SOAP₂: an improved ultrafast tool for short read alignment.Crossref | GoogleScholarGoogle Scholar | 19497933PubMed |

Li, Y, Liu, H, Wu, K, Liu, H, Huang, T, Chen, ZJ, Zhao, S, Ma, J, and Zhao, H (2019). Melatonin promotes human oocyte maturation and early embryo development by enhancing clathrin-mediated endocytosis. Journal of Pineal Research 67, e12601.
| Melatonin promotes human oocyte maturation and early embryo development by enhancing clathrin-mediated endocytosis.Crossref | GoogleScholarGoogle Scholar | 31361919PubMed |

Liang, QX, Lin, YH, Zhang, CH, Sun, HM, Zhou, L, Schatten, H, Sun, QY, and Qian, WP (2018). Resveratrol increases resistance of mouse oocytes to postovulatory aging in vivo. Aging (Albany, NY) 10, 1586–1596.
| Resveratrol increases resistance of mouse oocytes to postovulatory aging in vivo.Crossref | GoogleScholarGoogle Scholar | 30036861PubMed |

Lodde, V, Franciosi, F, Tessaro, I, Modina, SC, and Luciano, AM (2013). Role of gap junction-mediated communications in regulating large-scale chromatin configuration remodeling and embryonic developmental competence acquisition in fully grown bovine oocyte. Journal of Assisted Reproduction and Genetics 30, 1219–1226.
| Role of gap junction-mediated communications in regulating large-scale chromatin configuration remodeling and embryonic developmental competence acquisition in fully grown bovine oocyte.Crossref | GoogleScholarGoogle Scholar | 23881161PubMed |

Love, MI, Huber, W, and Anders, S (2014). Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biology 15, 550.
| Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.Crossref | GoogleScholarGoogle Scholar | 25516281PubMed |

Lu, JH, Wang, JZ, Wang, HL, Sui, HS, Liu, Y, Li, JJ, Liang, B, and Tan, JH (2010). Damaging effect of cumulus denudation on rabbit oocytes. Fertility and Sterility 93, 1567–1573.
| Damaging effect of cumulus denudation on rabbit oocytes.Crossref | GoogleScholarGoogle Scholar | 19589519PubMed |

Luciano, AM, Franciosi, F, Modina, SC, and Lodde, V (2011). Gap junction-mediated communications regulate chromatin remodeling during bovine oocyte growth and differentiation through cAMP-dependent mechanism(s). Biology of Reproduction 85, 1252–1259.
| Gap junction-mediated communications regulate chromatin remodeling during bovine oocyte growth and differentiation through cAMP-dependent mechanism(s).Crossref | GoogleScholarGoogle Scholar | 21816847PubMed |

Luciano, AM, Modina, S, Vassena, R, Milanesi, E, Lauria, A, and Gandolfi, F (2004). Role of intracellular cyclic adenosine 3′,5′-monophosphate concentration and oocyte–cumulus cells communications on the acquisition of the developmental competence during in vitro maturation of bovine oocyte. Biology of Reproduction 70, 465–472.
| Role of intracellular cyclic adenosine 3′,5′-monophosphate concentration and oocyte–cumulus cells communications on the acquisition of the developmental competence during in vitro maturation of bovine oocyte.Crossref | GoogleScholarGoogle Scholar | 14568913PubMed |

Macaulay, AD, Gilbert, I, Scantland, S, Fournier, E, Ashkar, F, Bastien, A, Shojaei Saadi, HA, Gagné, D, Sirard, MA, Khandjian, ÉW, Richard, FJ, Hyttel, P, and Robert, C (2016). Cumulus cell transcripts transit to the bovine oocyte in preparation for maturation. Biology of Reproduction 94, 16.
| Cumulus cell transcripts transit to the bovine oocyte in preparation for maturation.Crossref | GoogleScholarGoogle Scholar | 26586844PubMed |

Matzuk, MM, Burns, KH, Viveiros, MM, and Eppig, JJ (2002). Intercellular communication in the mammalian ovary: oocytes carry the conversation. Science 296, 2178–2180.
| Intercellular communication in the mammalian ovary: oocytes carry the conversation.Crossref | GoogleScholarGoogle Scholar | 12077402PubMed |

Mortazavi, A, Williams, BA, McCue, K, Schaeffer, L, and Wold, B (2008). Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nature Methods 5, 621–628.
| Mapping and quantifying mammalian transcriptomes by RNA-Seq.Crossref | GoogleScholarGoogle Scholar | 18516045PubMed |

Moussa, M, Li, MQ, Zheng, HY, Yang, CY, Yan, SF, Yu, NQ, Huang, JX, and Shang, JH (2018). Developmental competence of buffalo (Bubalus bubalis) denuded oocytes cocultured with cumulus cells: protective role of cumulus cells. Theriogenology 120, 40–46.
| Developmental competence of buffalo (Bubalus bubalis) denuded oocytes cocultured with cumulus cells: protective role of cumulus cells.Crossref | GoogleScholarGoogle Scholar | 30092373PubMed |

Nakamura, E, Otsuka, F, Terasaka, T, Inagaki, K, Hosoya, T, Tsukamoto-Yamauchi, N, Toma, K, and Makino, H (2014). Melatonin counteracts BMP-6 regulation of steroidogenesis by rat granulosa cells. Journal of Steroid Biochemistry and Molecular Biology 143, 233–239.
| Melatonin counteracts BMP-6 regulation of steroidogenesis by rat granulosa cells.Crossref | GoogleScholarGoogle Scholar |

Nogueira, D, Cortvrindt, R, De Matos, DG, Vanhoutte, L, and Smitz, J (2003). Effect of phosphodiesterase type 3 inhibitor on developmental competence of immature mouse oocytes in vitro. Biology of Reproduction 69, 2045–2052.
| Effect of phosphodiesterase type 3 inhibitor on developmental competence of immature mouse oocytes in vitro.Crossref | GoogleScholarGoogle Scholar | 12930710PubMed |

Norris, RP, Ratzan, WJ, Freudzon, M, Mehlmann, LM, Krall, J, Movsesian, MA, Wang, H, Ke, H, Nikolaev, VO, and Jaffe, LA (2009). Cyclic GMP from the surrounding somatic cells regulates cyclic AMP and meiosis in the mouse oocyte. Development 136, 1869–1878.
| Cyclic GMP from the surrounding somatic cells regulates cyclic AMP and meiosis in the mouse oocyte.Crossref | GoogleScholarGoogle Scholar | 19429786PubMed |

Nuttinck, F, Peynot, N, Humblot, P, Massip, A, Dessy, F, and Fléchon, JE (2000). Comparative immunohistochemical distribution of connexin 37 and connexin 43 throughout folliculogenesis in the bovine ovary. Molecular Reproduction and Development 57, 60–66.
| Comparative immunohistochemical distribution of connexin 37 and connexin 43 throughout folliculogenesis in the bovine ovary.Crossref | GoogleScholarGoogle Scholar | 10954857PubMed |

Peters, JL, Cassone, VM, and Zoran, MJ (2005). Melatonin modulates intercellular communication among cultured chick astrocytes. Brain Research 1031, 10–19.
| Melatonin modulates intercellular communication among cultured chick astrocytes.Crossref | GoogleScholarGoogle Scholar | 15621008PubMed |

Ratchford, AM, Esguerra, CR, and Moley, KH (2008). Decreased oocyte–granulosa cell gap junction communication and connexin expression in a type 1 diabetic mouse model. Molecular Endocrinology 22, 2643–2654.
| Decreased oocyte–granulosa cell gap junction communication and connexin expression in a type 1 diabetic mouse model.Crossref | GoogleScholarGoogle Scholar | 18829945PubMed |

Richard, S, and Baltz, JM (2014). Prophase I arrest of mouse oocytes mediated by natriuretic peptide precursor C requires GJA1 (connexin-43) and GJA4 (connexin-37) gap junctions in the antral follicle and cumulus–oocyte complex. Biology of Reproduction 90, 137.
| Prophase I arrest of mouse oocytes mediated by natriuretic peptide precursor C requires GJA1 (connexin-43) and GJA4 (connexin-37) gap junctions in the antral follicle and cumulus–oocyte complex.Crossref | GoogleScholarGoogle Scholar | 24804968PubMed |

Roemer, E, Lammerich, HP, Conroy, LL, and Weisensee, D (2013). Characterization of a gap-junctional intercellular communication (GJIC) assay using cigarette smoke. Toxicology Letters 219, 248–253.
| Characterization of a gap-junctional intercellular communication (GJIC) assay using cigarette smoke.Crossref | GoogleScholarGoogle Scholar | 23558295PubMed |

Rosenkrans, CF, and First, NL (1994). Effect of free amino acids and vitamins on cleavage and developmental rate of bovine zygotes in vitro. Journal of Animal Science 72, 434–437.
| Effect of free amino acids and vitamins on cleavage and developmental rate of bovine zygotes in vitro.Crossref | GoogleScholarGoogle Scholar | 8157527PubMed |

Salameh, A, Frenzel, C, Boldt, A, Rassler, B, Glawe, I, Schulte, J, Mühlberg, K, Zimmer, HG, Pfeiffer, D, and Dhein, S (2006). Subchronic alpha- and beta-adrenergic regulation of cardiac gap junction protein expression. FASEB Journal 20, 365–367.
| Subchronic alpha- and beta-adrenergic regulation of cardiac gap junction protein expression.Crossref | GoogleScholarGoogle Scholar | 16352648PubMed |

Sasseville, M, Gagnon, MC, Guillemette, C, Sullivan, R, Gilchrist, RB, and Richard, FJ (2009). Regulation of gap junctions in porcine cumulus–oocyte complexes: contributions of granulosa cell contact, gonadotropins, and lipid rafts. Molecular Endocrinology 23, 700–710.
| Regulation of gap junctions in porcine cumulus–oocyte complexes: contributions of granulosa cell contact, gonadotropins, and lipid rafts.Crossref | GoogleScholarGoogle Scholar | 19228792PubMed |

Shu, C, Huang, W, Zeng, Z, He, Y, Luo, B, Liu, H, Li, J, and Xu, J (2017). Connexin 43 is involved in the sympathetic atrial fibrillation in canine and canine atrial myocytes. Anatolian Journal of Cardiology 18, 3–9.
| Connexin 43 is involved in the sympathetic atrial fibrillation in canine and canine atrial myocytes.Crossref | GoogleScholarGoogle Scholar | 28554986PubMed |

Simon, AM, Chen, H, and Jackson, CL (2006). Cx37 and Cx43 localize to zona pellucida in mouse ovarian follicles. Cell Communication and Adhesion 13, 61–77.
| Cx37 and Cx43 localize to zona pellucida in mouse ovarian follicles.Crossref | GoogleScholarGoogle Scholar | 16613781PubMed |

Simon, AM, Goodenough, DA, Li, E, and Paul, DL (1997). Female infertility in mice lacking connexin 37. Nature 385, 525–529.
| Female infertility in mice lacking connexin 37.Crossref | GoogleScholarGoogle Scholar | 9020357PubMed |

Söhl, G, and Willecke, K (2004). Gap junctions and the connexin protein family. Cardiovascular Research 62, 228–232.
| Gap junctions and the connexin protein family.Crossref | GoogleScholarGoogle Scholar | 15094343PubMed |

Strieder-Barboza, C, and Contreras, GA (2019). Fetuin-A modulates lipid mobilization in bovine adipose tissue by enhancing lipogenic activity of adipocytes. Journal of Dairy Science 102, 4628–4638.
| Fetuin-A modulates lipid mobilization in bovine adipose tissue by enhancing lipogenic activity of adipocytes.Crossref | GoogleScholarGoogle Scholar | 30827564PubMed |

Sugimura, S, Yamanouchi, T, Palmerini, MG, Hashiyada, Y, Imai, K, and Gilchrist, RB (2018). Effect of pre-in vitro maturation with cAMP modulators on the acquisition of oocyte developmental competence in cattle. Journal of Reproduction and Development 64, 233–241.
| Effect of pre-in vitro maturation with cAMP modulators on the acquisition of oocyte developmental competence in cattle.Crossref | GoogleScholarGoogle Scholar |

Sugiura, K, Pendola, FL, and Eppig, JJ (2005). Oocyte control of metabolic cooperativity between oocytes and companion granulosa cells: energy metabolism. Developmental Biology 279, 20–30.
| Oocyte control of metabolic cooperativity between oocytes and companion granulosa cells: energy metabolism.Crossref | GoogleScholarGoogle Scholar | 15708555PubMed | 15708555PubMed |

Takens-Kwak, BR, Jongsma, HJ, Rook, MB, and Van Ginneken, AC (1992). Mechanism of heptanol-induced uncoupling of cardiac gap junctions: a perforated patch-clamp study. American Journal of Physiology 262, C1531–C1538.
| Mechanism of heptanol-induced uncoupling of cardiac gap junctions: a perforated patch-clamp study.Crossref | GoogleScholarGoogle Scholar |

Talhouk, R, Tarraf, C, Kobrossy, L, Shaito, A, Bazzi, S, Bazzoun, D, and El-Sabban, M (2012). Modulation of Cx43 and gap junctional intercellular communication by androstenedione in rat polycystic ovary and granulosa cells in vitro. Journal of Reproduction & Infertility 13, 21–32.

Tan, D-X, and Reiter, RJ (2019). Mitochondria: the birth place, battle ground and the site of melatonin metabolism in cells. Melatonin Research 2, 44–66.
| Mitochondria: the birth place, battle ground and the site of melatonin metabolism in cells.Crossref | GoogleScholarGoogle Scholar |

Tang, F, Barbacioru, C, Nordman, E, Li, B, Xu, N, Bashkirov, VI, Lao, K, and Azim Surani, M (2010). RNA-Seq analysis to capture the transcriptome landscape of a single cell. Nature Protocols 5, 516–535.
| RNA-Seq analysis to capture the transcriptome landscape of a single cell.Crossref | GoogleScholarGoogle Scholar | 20203668PubMed | 20203668PubMed |

Teilmann, SC (2005). Differential expression and localisation of connexin-37 and connexin-43 in follicles of different stages in the 4-week-old mouse ovary. Molecular and Cellular Endocrinology 234, 27–35.
| Differential expression and localisation of connexin-37 and connexin-43 in follicles of different stages in the 4-week-old mouse ovary.Crossref | GoogleScholarGoogle Scholar | 15836950PubMed | 15836950PubMed |

Tian, X, Wang, F, He, C, Zhang, L, Tan, D, Reiter, RJ, Xu, J, Ji, P, and Liu, G (2014). Beneficial effects of melatonin on bovine oocytes maturation: a mechanistic approach. Journal of Pineal Research 57, 239–247.
| Beneficial effects of melatonin on bovine oocytes maturation: a mechanistic approach.Crossref | GoogleScholarGoogle Scholar | 25070516PubMed | 25070516PubMed |

Vaccari, S, Weeks, JL, Hsieh, M, Menniti, FS, and Conti, M (2009). Cyclic GMP signaling is involved in the luteinizing hormone-dependent meiotic maturation of mouse oocytes. Biology of Reproduction 81, 595–604.
| Cyclic GMP signaling is involved in the luteinizing hormone-dependent meiotic maturation of mouse oocytes.Crossref | GoogleScholarGoogle Scholar | 19474061PubMed | 19474061PubMed |

Wang, S, Liu, B, Liu, W, Xiao, Y, Zhang, H, and Yang, L (2017). The effects of melatonin on bovine uniparental embryos development in vitro and the hormone secretion of COCs. PeerJ 5, e3485.
| The effects of melatonin on bovine uniparental embryos development in vitro and the hormone secretion of COCs.Crossref | GoogleScholarGoogle Scholar | 28698819PubMed | 28698819PubMed |

Wigglesworth, K, Lee, KB, O’Brien, MJ, Peng, J, Matzuk, MM, and Eppig, JJ (2013). Bidirectional communication between oocytes and ovarian follicular somatic cells is required for meiotic arrest of mammalian oocytes. Proceedings of the National Academy of Sciences of the United States of America 110, E3723–E3729.
| Bidirectional communication between oocytes and ovarian follicular somatic cells is required for meiotic arrest of mammalian oocytes.Crossref | GoogleScholarGoogle Scholar | 23980176PubMed | 23980176PubMed |

Winterhager, E, and Kidder, GM (2015). Gap junction connexins in female reproductive organs: implications for women’s reproductive health. Human Reproduction Update 21, 340–352.
| Gap junction connexins in female reproductive organs: implications for women’s reproductive health.Crossref | GoogleScholarGoogle Scholar | 25667189PubMed | 25667189PubMed |

Xi, G, An, L, Jia, Z, Tan, K, Zhang, J, Wang, Z, Zhang, C, Miao, K, Wu, Z, and Tian, J (2018). Natriuretic peptide receptor 2 (NPR2) localized in bovine oocyte underlies a unique mechanism for C-type natriuretic peptide (CNP)-induced meiotic arrest. Theriogenology 106, 198–209.
| Natriuretic peptide receptor 2 (NPR2) localized in bovine oocyte underlies a unique mechanism for C-type natriuretic peptide (CNP)-induced meiotic arrest.Crossref | GoogleScholarGoogle Scholar | 29080478PubMed | 29080478PubMed |

Xia, Y, Gong, KZ, Xu, M, Zhang, YY, Guo, JH, Song, Y, and Zhang, P (2009). Regulation of gap-junction protein connexin 43 by beta-adrenergic receptor stimulation in rat cardiomyocytes. Acta Pharmacologica Sinica 30, 928–934.
| Regulation of gap-junction protein connexin 43 by beta-adrenergic receptor stimulation in rat cardiomyocytes.Crossref | GoogleScholarGoogle Scholar | 19574999PubMed | 19574999PubMed |

Yang, M, Tao, J, Chai, M, Wu, H, Wang, J, Li, G, He, C, Xie, L, Ji, P, Dai, Y, Yang, L, and Liu, G (2017). Melatonin improves the quality of inferior bovine oocytes and promoted their subsequent IVF embryo development: mechanisms and results. Molecules 22, 2059.
| Melatonin improves the quality of inferior bovine oocytes and promoted their subsequent IVF embryo development: mechanisms and results.Crossref | GoogleScholarGoogle Scholar |

Yuan, D, Li, X, Luo, C, Li, X, Cheng, N, Ji, H, Qiu, R, Luo, G, Chen, C, and Hei, Z (2019). Inhibition of gap junction composed of Cx43 prevents against acute kidney injury following liver transplantation. Cell Death and Disease 10, 767.
| Inhibition of gap junction composed of Cx43 prevents against acute kidney injury following liver transplantation.Crossref | GoogleScholarGoogle Scholar | 31601792PubMed | 31601792PubMed |

Yuan, Y, Spate, LD, Redel, BK, Tian, Y, Zhou, J, Prather, RS, and Michael Roberts, R (2017). Quadrupling efficiency in production of genetically modified pigs through improved oocyte maturation. Proceedings of the National Academy of Sciences of the United States of America 114, E5796–E5804.
| Quadrupling efficiency in production of genetically modified pigs through improved oocyte maturation.Crossref | GoogleScholarGoogle Scholar | 28673989PubMed | 28673989PubMed |

Zhang, Y, Hou, MC, Li, JJ, Qi, Y, Zhang, Y, She, G, Ren, YJ, Wu, W, Pang, ZD, Xie, W, Deng, XL, and Du, XJ (2020). Cardiac β-adrenergic receptor activation mediates distinct and cell type-dependent changes in the expression and distribution of connexin 43. Journal of Cellular and Molecular Medicine 24, 8505–8517.
| Cardiac β-adrenergic receptor activation mediates distinct and cell type-dependent changes in the expression and distribution of connexin 43.Crossref | GoogleScholarGoogle Scholar | 32578931PubMed | 32578931PubMed |

Zhao, X, Du, F, Liu, X, Ruan, Q, Wu, Z, Lei, C, Deng, Y, Luo, C, Jiang, J, Shi, D, and Lu, F (2019). Brain-derived neurotrophic factor (BDNF) is expressed in buffalo (Bubalus bubalis) ovarian follicles and promotes oocyte maturation and early embryonic development. Theriogenology 130, 79–88.
| Brain-derived neurotrophic factor (BDNF) is expressed in buffalo (Bubalus bubalis) ovarian follicles and promotes oocyte maturation and early embryonic development.Crossref | GoogleScholarGoogle Scholar | 30877846PubMed | 30877846PubMed |

Zhao, XM, Min, JT, Du, WH, Hao, HS, Liu, Y, Qin, T, Wang, D, and Zhu, HB (2015). Melatonin enhances the in vitro maturation and developmental potential of bovine oocytes denuded of the cumulus oophorus. Zygote 23, 525–536.
| Melatonin enhances the in vitro maturation and developmental potential of bovine oocytes denuded of the cumulus oophorus.Crossref | GoogleScholarGoogle Scholar | 24869483PubMed | 24869483PubMed |

Zhao, XM, Wang, N, Hao, HS, Li, CY, Zhao, YH, Yan, CL, Wang, HY, Du, WH, Wang, D, Liu, Y, Pang, YW, and Zhu, HB (2018). Melatonin improves the fertilization capacity and developmental ability of bovine oocytes by regulating cytoplasmic maturation events. Journal of Pineal Research 64, e12445.
| Melatonin improves the fertilization capacity and developmental ability of bovine oocytes by regulating cytoplasmic maturation events.Crossref | GoogleScholarGoogle Scholar |

Zhuan, Q, Ma, H, Chen, J, Luo, Y, Luo, Y, Gao, L, Hou, Y, Zhu, S, and Fu, X (2020). Cytoplasm lipids can be modulated through hormone-sensitive lipase and are related to mitochondrial function in porcine IVM oocytes. Reproduction, Fertility and Development 32, 667–675.
| Cytoplasm lipids can be modulated through hormone-sensitive lipase and are related to mitochondrial function in porcine IVM oocytes.Crossref | GoogleScholarGoogle Scholar |

Zizzadoro, C, Caruso, M, Punzi, S, Crescenzo, G, Zongoli, F, and Belloli, C (2018). A comparative study between responses of isolated bovine and equine digital arteries to vasoactive mediators. Journal of Veterinary Pharmacology and Therapeutics 41, 51–59.
| A comparative study between responses of isolated bovine and equine digital arteries to vasoactive mediators.Crossref | GoogleScholarGoogle Scholar | 28703351PubMed | 28703351PubMed |

Zou, H, Chen, B, Ding, D, Gao, M, Chen, D, Liu, Y, Hao, Y, Zou, W, Ji, D, Zhou, P, Wei, Z, Cao, Y, and Zhang, Z (2020). Melatonin promotes the development of immature oocytes from the COH cycle into healthy offspring by protecting mitochondrial function. Journal of Pineal Research 68, e12621.
| Melatonin promotes the development of immature oocytes from the COH cycle into healthy offspring by protecting mitochondrial function.Crossref | GoogleScholarGoogle Scholar | 31714635PubMed | 31714635PubMed |