Evaluation of viability, developmental competence, and apoptosis-related transcripts during in vivo post-ovulatory oocyte aging in zebrafish Danio rerio (Hamilton, 1822)

. 2024 ; 11 () : 1389070. [epub] 20240617

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid38952806

INTRODUCTION: Post-ovulatory aging is a time-dependent deterioration of ovulated oocytes and a major limiting factor reducing the fitness of offspring. This process may lead to the activation of cell death pathways like apoptosis in oocytes. METHODOLOGY: We evaluated oocyte membrane integrity, egg developmental competency, and mRNA abundance of apoptosis-related genes by RT-qPCR. Oocytes from zebrafish Danio rerio were retained in vivo at 28.5°C for 24 h post-ovulation (HPO). Viability was assessed using trypan blue (TB) staining. The consequences of in vivo oocyte aging on the developmental competence of progeny were determined by the embryo survival at 24 h post fertilization, hatching, and larval malformation rates. RESULTS: The fertilization, oocyte viability, and hatching rates were 91, 97, and 65% at 0 HPO and dropped to 62, 90, and 22% at 4 HPO, respectively. The fertilizing ability was reduced to 2% at 8 HPO, while 72% of oocytes had still intact plasma membranes. Among the apoptotic genes bcl-2 (b-cell lymphoma 2), bada (bcl2-associated agonist of cell death a), cathepsin D, cathepsin Z, caspase 6a, caspase 7, caspase 8, caspase 9, apaf1, tp53 (tumor protein p53), cdk1 (cyclin-dependent kinase 1) studied, mRNA abundance of anti-apoptotic bcl-2 decreased and pro-apoptotic cathepsin D increased at 24 HPO. Furthermore, tp53 and cdk1 mRNA transcripts decreased at 24 HPO compared to 0 HPO. DISCUSSION: Thus, TB staining did not detect the loss of oocyte competency if caused by aging. TB staining, however, could be used as a simple and rapid method to evaluate the quality of zebrafish oocytes before fertilization. Taken together, our results indicate the activation of cell death pathways in the advanced stages of oocyte aging in zebrafish.

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Bobe J, Labbé C. Egg and sperm quality in fish. Gen Comp Endocrinol. (2010) 165:535–48. doi: 10.1016/j.ygcen.2009.02.011 PubMed DOI

Tarin JJ, Perez-Albala S, Cano A. Consequences on offspring of abnormal function in ageing gametes. Hum Reprod Update. (2000) 6:532–49. doi: 10.1093/humupd/6.6.532, PMID: PubMed DOI

Takahashi T, Takahashi E, Igarashi H, Tezuka N, Kurachi H. Impact of oxidative stress in aged mouse oocytes on calcium oscillations at fertilization. Mol Reprod Dev. (2003) 66:143–52. doi: 10.1002/mrd.10341, PMID: PubMed DOI

Perez GI, Trbovich AM, Gosden RG, Tilly JL. Mitochondria and the death of oocytes. Nature. (2000) 403:500–1. doi: 10.1038/35000651 PubMed DOI

Hamatani T, Falco G, Carter MG, Akutsu H, Stagg CA, Sharov AA, et al. . Age-associated alteration of gene expression patterns in mouse oocytes. Hum Mol Genet. (2004) 13:2263–78. doi: 10.1093/hmg/ddh241, PMID: PubMed DOI

Takahashi T, Igarashi H, Amita M, Hara S, Kurachi H. Cellular and molecular mechanisms of various types of oocyte aging. Reprod Med Biol. (2011) 10:239–49. doi: 10.1007/s12522-011-0099-0, PMID: PubMed DOI PMC

Kosubek A, Klein-Hitpass L, Rademacher K, Horsthemke B, Ryffel GU. Aging of Xenopus tropicalis eggs leads to deadenylation of a specific set of maternal mRNAs and loss of developmental potential. PLoS One. (2010) 5:e13532. doi: 10.1371/journal.pone.0013532, PMID: PubMed DOI PMC

Dankert D, Demond H, Trapphoff T, Heiligentag M, Rademacher K, Eichenlaub-Ritter U, et al. . Pre-and postovulatory aging of murine oocytes affect the transcript level and poly (a) tail length of maternal effect genes. PLoS One. (2014) 9:e108907. doi: 10.1371/journal.pone.0108907, PMID: PubMed DOI PMC

Ma W, Zhang D, Hou Y, Li Y-H, Sun Q-Y, Sun X-F, et al. . Reduced expression of MAD2, BCL2, and MAP kinase activity in pig oocytes after in vitro aging are associated with defects in sister chromatid segregation during meiosis II and embryo fragmentation after activation. Biol Reprod. (2005) 72:373–83. doi: 10.1095/biolreprod.104.030999, PMID: PubMed DOI

Tatone C, Carbone MC, Gallo R, Delle Monache S, Di Cola M, Alesse E, et al. . Age-associated changes in mouse oocytes during postovulatory in vitro culture: possible role for meiotic kinases and survival factor BCL21. Biol Reprod. (2006) 74:395–402. doi: 10.1095/biolreprod.105.046169, PMID: PubMed DOI

Huang J-C, Yan L-Y, Lei Z-L, Miao Y-L, Shi L-H, Yang J-W, et al. . Changes in histone acetylation during postovulatory aging of mouse oocyte. Biol Reprod. (2007) 77:666–70. doi: 10.1095/biolreprod.107.062703, PMID: PubMed DOI

Ge Z-J, Schatten H, Zhang C-L, Sun Q-Y. Oocyte ageing and epigenetics. Reproduction. (2015) 149:R103–14. doi: 10.1530/REP-14-0242, PMID: PubMed DOI PMC

Perez GI, Tao X-J, Tilly JL. Fragmentation and death (aka apoptosis) of ovulated oocytes. Mol Hum Reprod. (1999) 5:414–20. doi: 10.1093/molehr/5.5.414, PMID: PubMed DOI

Gordo AC, Rodrigues P, Kurokawa M, Jellerette T, Exley GE, Warner C, et al. . Intracellular calcium oscillations signal apoptosis rather than activation in in vitro aged mouse eggs. Biol Reprod. (2002) 66:1828–37. doi: 10.1095/biolreprod66.6.1828, PMID: PubMed DOI

Tokmakov AA, Sato K-I, Stefanov VE. Postovulatory cell death: why eggs die via apoptosis in biological species with external fertilization. J Reprod Dev. (2017) 64:1–6. doi: 10.1262/jrd.2017-100 PubMed DOI PMC

Ma H, Weber GM, Hostuttler MA, Wei H, Wang L, Yao J. MicroRNA expression profiles from eggs of different qualities associated with post-ovulatory ageing in rainbow trout (Oncorhynchus mykiss). BMC Genomics. (2015) 16:201. doi: 10.1186/s12864-015-1400-0, PMID: PubMed DOI PMC

Samarin A, Samarin A, Østbye T-KK, Ruyter B, Sampels S, Burkina V, et al. . Alteration of mRNA abundance, oxidation products and antioxidant enzyme activities during oocyte ageing in common carp Cyprinus carpio. PLoS One. (2019) 14:e0212694. doi: 10.1371/journal.pone.0212694, PMID: PubMed DOI PMC

Samarin AM, Samarin AM, Østbye T-KK, Ruyter B, Sampels S, Burkina V, et al. . The possible involvement of oxidative stress in the oocyte ageing process in goldfish Carassius auratus (Linnaeus, 1758). Sci Rep. (2019) 9:10469. doi: 10.1038/s41598-019-46895-1 PubMed DOI PMC

Waghmare SG, Samarin AM, Samarin AM, Danielsen M, Møller HS, Policar T, et al. . Histone acetylation dynamics during in vivo and in vitro oocyte aging in common carp Cyprinus carpio. Int J Mol Sci. (2021) 22:6036. doi: 10.3390/ijms22116036, PMID: PubMed DOI PMC

Samarin AM, Policar T, Lahnsteiner F. Fish oocyte ageing and its effect on egg quality. Rev Fish Sci Aquacul. (2015) 23:302–14. doi: 10.1080/23308249.2015.1053560 DOI

Rizzo E, Godinho HP, Sato Y. Short-term storage of oocytes from the neotropical teleost fish Prochilodus marggravii. Theriogenology. (2003) 60:1059–70. doi: 10.1016/S0093-691X(03)00108-0, PMID: PubMed DOI

Niksirat H, Sarvi K, Amiri BM, Karami M, Hatef A. In vitro storage of unfertilized ova of endangered Caspian brown trout (Salmo trutta caspius) in artificial media. Anim Reprod Sci. (2007) 100:356–63. doi: 10.1016/j.anireprosci.2006.08.019, PMID: PubMed DOI

Bahre Kazemi M, Soltani M, Matinfar A, Abtahi B, Pusti I, SamarinA M, et al. . Biochemical and histological studies of over-ripened oocyte in the Caspian brown trout (Salmo trutta caspius) to determine biomarkers for egg quality. Iran J Fish Sci. (2010) 9:33–48. doi: 10.22092/IJFS.2018.114081 DOI

Niksirat H, Sarvi K, Amiri BM, Hatef A. Effects of storage duration and storage media on initial and post-eyeing mortality of stored ova of rainbow trout Oncorhynchus mykiss. Aquaculture. (2007) 262:528–31. doi: 10.1016/j.aquaculture.2006.10.031 DOI

Samarin AM, Ahmadi MR, Azuma T, Rafiee GR, Amiri BM, Naghavi MR. Influence of the time to egg stripping on eyeing and hatching rates in rainbow trout Oncorhynchus mykiss under cold temperatures. Aquaculture. (2008) 278:195–8. doi: 10.1016/j.aquaculture.2008.03.034 DOI

Samarin AM, Blecha M, Uzhytchak M, Bytyutskyy D, Zarski D, Flajshans M, et al. . Post-ovulatory and post-stripping oocyte ageing in northern pike, Esox lucius (Linnaeus, 1758), and its effect on egg viability rates and the occurrence of larval malformations and ploidy anomalies. Aquaculture. (2016) 450:431–8. doi: 10.1016/j.aquaculture.2015.08.017 DOI

Westerfield M. The zebrafish book. A guide for the laboratory use of Zebrafish (Danio rerio), 4th Edition. Eugene: University of Oregon Press; (2000).

Strober W. Trypan blue exclusion test of cell viability. Curr Protoc Immunol. (2015) 111:A–3B. doi: 10.1002/0471142735.ima03bs111 PubMed DOI PMC

Rodina M, Cosson J, Gela D, Linhart O. Kurokura solution as immobilizing medium for spermatozoa of Tench (Tinca tinca L.). Aquac Int. (2004) 12:119–31. doi: 10.1023/B:AQUI.0000017192.75993.e3 DOI

Fauvel C, Suquet M, Cosson J. Evaluation of fish sperm quality. J Appl Ichthyol. (2010) 26:636–43. doi: 10.1111/j.1439-0426.2010.01529.x DOI

Waghmare SG, Samarin AM, Franěk R, Pšenička M, Policar T, Linhart O, et al. . Oocyte ageing in zebrafish Danio rerio (Hamilton, 1822) and its consequence on the viability and ploidy anomalies in the progeny. Animals. (2021) 11:912. doi: 10.3390/ani11030912, PMID: PubMed DOI PMC

Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. (2001) 25:402–8. doi: 10.1006/meth.2001.1262 PubMed DOI

Samarin AM, Sampels S, Policar T, Rodina M, Hematyar N, Samarin AM. mRNA abundance changes during in vitro oocyte ageing in African catfish Clarias gariepinus (Burchell, 1822). Aquac Res. (2018) 49:1037–45. doi: 10.1111/are.13552 DOI

Azuma T, Ohta H, Oda S, Muto K, Yada T, Unuma T. Changes in fertility of rainbow trout eggs retained in coelom. Fish Sci. (2003) 69:131–6. doi: 10.1046/j.1444-2906.2003.00597.x DOI

Nomura K, Takeda Y, Unuma T, Morishima K, Tanaka H, Arai K, et al. . Post-ovulatory oocyte aging induces spontaneous occurrence of polyploids and mosaics in artificial fertilization of Japanese eel, Anguilla japonica. Aquaculture. (2013) 404-405:15–21. doi: 10.1016/j.aquaculture.2013.04.016 DOI

Samarin AM, Blecha M, Bytyutskyy D, Policar T. Post-ovulatory oocyte ageing in pikeperch (Sander lucioperca L.) and its effect on egg viability rates and the occurrence of larval malformations and ploidy anomalies. Turk J Fish Aquat Sci. (2015) 15:429–35. doi: 10.4194/1303-2712-v15_2_29 DOI

do Nascimento NF, Lázaro TM, de Alcântara NR, Senhorini JA, dos Santos SCA, Nakaghi LSO, et al. . In vivo storage of oocytes leads to lower survival, increased abnormalities and may affect the ploidy status in the yellowtail tetra Astyanax altiparanae. Zygote. (2018) 26:471–5. doi: 10.1017/S0967199418000527, PMID: PubMed DOI

Siripattarapravat K, Busta A, Steibel JP, Cibelli J. Characterization and in vitro control of MPF activity in zebrafish eggs. Zebrafish. (2009) 6:97–105. doi: 10.1089/zeb.2008.0527, PMID: PubMed DOI

Cardona-Costa J, Perez-Camps M, Garcia-Ximenez F, Espinos FJ. Effect of gametes aging on their activation and fertilizability in zebrafish (Danio rerio). Zebrafish. (2009) 6:93–5. doi: 10.1089/zeb.2008.0578, PMID: PubMed DOI

Rime H, Guitton N, Pineau C, Bonnet E, Bobe J, Jalabert B. Post-ovulatory ageing and egg quality: a proteomic analysis of rainbow trout coelomic fluid. Reprod Biol Endocrinol. (2004) 2:26. doi: 10.1186/1477-7827-2-26, PMID: PubMed DOI PMC

Kågedal K, Johansson U, Öllinger K. The lysosomal protease cathepsin D mediates apoptosis induced by oxidative stress. FASEB J. (2001) 15:1592–4. doi: 10.1096/fj.00-0708fje PubMed DOI

Paquet C, Sane A, Beauchemin M, Bertrand R. Caspase-and mitochondrial dysfunction-dependent mechanisms of lysosomal leakage and cathepsin B activation in DNA damage-induced apoptosis. Leukemia. (2005) 19:784–91. doi: 10.1038/sj.leu.2403717, PMID: PubMed DOI

Carnevali O, Polzonetti V, Cardinali M, Pugnaloni A, Natalini P, Zmora N, et al. . Apoptosis in sea bream Sparus aurata eggs. Mol Reprod Dev. (2003) 66:291–6. doi: 10.1002/mrd.10356, PMID: PubMed DOI

Aegerter S, Jalabert B, Bobe J. Large scale real-time PCR analysis of mRNA abundance in rainbow trout eggs in relationship with egg quality and post-ovulatory ageing. Mol Reprod Dev. (2005) 72:377–85. doi: 10.1002/mrd.20361, PMID: PubMed DOI

Lubzens E, Bobe J, Young G, Sullivan CV. Maternal investment in fish oocytes and eggs: the molecular cargo and its contributions to fertility and early development. Aquaculture. (2017) 472:107–43. doi: 10.1016/j.aquaculture.2016.10.029 DOI

Conus S, Perozzo R, Reinheckel T, Peters C, Scapozza L, Yousefi S, et al. . Caspase-8 is activated by cathepsin D initiating neutrophil apoptosis during the resolution of inflammation. J Exp Med. (2008) 205:685–98. doi: 10.1084/jem.20072152, PMID: PubMed DOI PMC

Adams JM, Cory S. The Bcl-2 protein family: arbiters of cell survival. Science. (1998) 281:1322–6. doi: 10.1126/science.281.5381.1322, PMID: PubMed DOI

Xu Z, Abbott A, Kopf GS, Schultz RM, Ducibella T. Spontaneous activation of ovulated mouse eggs: time-dependent effects on M-phase exit, cortical granule exocytosis, maternal messenger ribonucleic acid recruitment, and inositol 1, 4, 5-trisphosphate sensitivity. Biol Reprod. (1997) 57:743–50. doi: 10.1095/biolreprod57.4.743, PMID: PubMed DOI

Nakano K, Vousden KH. PUMA, a novel proapoptotic gene, is induced by p53. Mol Cell. (2001) 7:683–94. doi: 10.1016/S1097-2765(01)00214-3, PMID: PubMed DOI

Miyashita T, Reed JC. Tumor suppressor p53 is a direct transcriptional activator of the human bax gene. Cell. (1995) 80:293–9. doi: 10.1016/0092-8674(95)90412-3, PMID: PubMed DOI

Robles AI, Bemmels NA, Foraker AB, Harris CC. APAF-1 is a transcriptional target of p53 in DNA damage-induced apoptosis. Cancer Res. (2001) 61:6660–4. PMID: PubMed

Yu J, Zhang L. The transcriptional targets of p53 in apoptosis control. Biochem Biophys Res Commun. (2005) 331:851–8. doi: 10.1016/j.bbrc.2005.03.189, PMID: PubMed DOI

Aegerter S, Jalabert B, Bobe J. Messenger RNA stockpile of cyclin B, insulin-like growth factor I, insulin-like growth factor II, insulin-like growth factor receptor Ib, and p53 in the rainbow trout oocyte in relation with developmental competence. Mol Reprod Dev. (2004) 67:127–35. doi: 10.1002/mrd.10384, PMID: PubMed DOI

Guglielmino MR, Santonocito M, Vento M, Ragusa M, Barbagallo D, Borzì P, et al. . TAp73 is downregulated in oocytes from women of advanced reproductive age. Cell Cycle. (2011) 10:3253–6. doi: 10.4161/cc.10.19.17585, PMID: PubMed DOI PMC

Jeon H-J, Cui X-S, Guo J, Lee JM, Kim J-S, Oh JS. TCTP regulates spindle assembly during postovulatory aging and prevents deterioration in mouse oocyte quality. Biochimica et Biophysica Acta (BBA) - molecular. Cell Res. (2017) 1864:1328–34. doi: 10.1016/j.bbamcr.2017.05.002 PubMed DOI

Wang T, Gao YY, Chen L, Nie ZW, Cheng W, Liu X, et al. . Melatonin prevents postovulatory oocyte aging and promotes subsequent embryonic development in the pig. Aging. (2017) 9:1552–64. doi: 10.18632/aging.101252, PMID: PubMed DOI PMC

Armstrong JF, Kaufman MH, Harrison DJ, Clarke AR. High-frequency developmental abnormalities in p53-deficient mice. Curr Biol. (1995) 5:931–6. doi: 10.1016/S0960-9822(95)00183-7, PMID: PubMed DOI

Wallingford JB, Seufert DW, Virta VC, Vize PD. p53 activity is essential for normal development in Xenopus. Curr Biol. (1997) 7:747–57. doi: 10.1016/S0960-9822(06)00333-2, PMID: PubMed DOI

Masui Y, Markert CL. Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes. J Exp Zool. (1971) 177:129–45. doi: 10.1002/jez.1401770202, PMID: PubMed DOI

Adhikari D, Zheng W, Shen Y, Gorre N, Ning Y, Halet G, et al. . Cdk1, but not Cdk2, is the sole Cdk that is essential and sufficient to drive resumption of meiosis in mouse oocytes. Hum Mol Genet. (2012) 21:2476–84. doi: 10.1093/hmg/dds061, PMID: PubMed DOI

Iguchi S, Iwasaki T, Fukami Y, Tokmakov AA. Unlaid Xenopus eggs degrade by apoptosis in the genital tract. BMC Cell Biol. (2013) 14:11. doi: 10.1186/1471-2121-14-11 PubMed DOI PMC

Tokmakov AA, Iguchi S, Iwasaki T, Fukami Y. Unfertilized frog eggs die by apoptosis following meiotic exit. BMC Cell Biol. (2011) 12:56. doi: 10.1186/1471-2121-12-56, PMID: PubMed DOI PMC

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