Fol. Biol. 2021, 67, 208-212
https://doi.org/10.14712/fb2021067050208
Prostaglandin F2α Causes Fast Degenerative Changes in Ovulated Mouse Oocytes
References
1. , C. E., Jungheim, E. S. (2015) Inflammation and human ovarian follicular dynamics. Semin. Reprod. Med. 33, 270-275.
<https://doi.org/10.1055/s-0035-1554928>
2. , J. J., Sheldon, I. M. (2011) Lipopolysaccharide initiates inflammation in bovine granulosa cells via the TLR4 pathway and perturbs oocyte meiotic progression in vitro. Endocrinology 152, 5029-5040.
<https://doi.org/10.1210/en.2011-1124>
3. , C., Lindberg, R., Figueroa, R., Gudise, S., Onischenko, E., Hallberg, E. (2009) An integral protein of the inner nuclear membrane localizes to the mitotic spindle in mammalian cells. J. Cell. Sci. 122 (Pt 12), 2100-2107.
<https://doi.org/10.1242/jcs.047373>
4. , S. H., Lee, S. (2021) Prostaglandin F2α triggers the disruption of cell adhesion with cytokeratin and vimentin in bovine luteal theca cells. Animals (Basel) 11, 1073.
<https://doi.org/10.3390/ani11041073>
5. , Y., Zhou, C., Cui, Z., Zhang, M., ShiYang, X., Lu, Y., Xiong, B. (2018) Postovulatory aging causes the deterioration of porcine oocytes via induction of oxidative stress. FASEB J. 32, 1328-1337.
<https://doi.org/10.1096/fj.201700908R>
6. , V., Delimitreva, S., Chakarova, I., Zhivkova, R., Hadzhinesheva, V., Markova, M. (2017) Dynamics of lamins B and A/C and nucleoporin Nup160 during meiotic maturation in mouse oocytes. Folia Biol. (Praha) 63, 6-12.
7. , S., Tiwari, M., Koch, B., Chaube, S. K. (2015) Morphological, cellular and molecular changes during postovulatory egg aging in mammals. J. Biomed. Sci. 22, 36.
<https://doi.org/10.1186/s12929-015-0143-1>
8. , S. A. D, Pontelo, T. P., Kussano, N. R., Kawamoto, T. S., Leme, L. O., Caixeta, F. M. C., Pfeifer, L. F. M., Franco, M. M., Dode, M. A. N. (2020) Effects of prostaglandins E2 and F2α on the in vitro maturation of bovine oocytes. Domest. Anim. Endocrinol. 72, 106447.
<https://doi.org/10.1016/j.domaniend.2020.106447>
9. , M. (2012) Regulation of oocyte meiotic maturation by somatic cells. Reprod. Med. Biol. 11, 177-184.
<https://doi.org/10.1007/s12522-012-0130-0>
10. , P., Natzke, R. P., Hansen, P. J. (2003) Identification of possible mediators of embryonic mortality caused by mastitis: actions of lipopolysaccharide, prostaglandin F2α, and the nitric oxide generator, sodium nitroprusside dihydrate, on oocyte maturation and embryonic development in cattle. Am. J. Reprod. Immunol. 50, 263-272.
<https://doi.org/10.1034/j.1600-0897.2003.00085.x>
11. , H., Satoh, M., Toyokawa, K. (2005) Changes in distribution of active mitochondria during oocyte maturation and fertilization in the hamster. J. Mamm. Ova Res. 22, 163-169.
<https://doi.org/10.1274/jmor.22.163>
12. , Y., Hashimoto, S., Yamochi, T., Goto, H., Yamanaka, M., Amo, A., Matsumoto, H., Inoue, M., Ito, K., Nakaoka, Y., Suzuki, N., Morimoto, Y. (2016) Dynamic changes in mitochondrial distribution in human oocytes during meiotic maturation. J. Assist. Reprod. Genet. 33, 929-938.
<https://doi.org/10.1007/s10815-016-0716-2>
13. , J., Runner, M. N. (1984) Mitochondrial reorganization during resumption of arrested meiosis in the mouse oocyte. Am. J. Anat. 171, 335-355.
<https://doi.org/10.1002/aja.1001710309>
14. , T., Gao, Y. Y., Chen, L., Nie, Z. W., Cheng, W., Liu, X., Schatten, H., Zhang, X., Miao, Y. L. (2017) Melatonin prevents postovulatory oocyte aging and promotes subsequent embryonic development in the pig. Aging (Albany NY) 9, 1552-1564.
<https://doi.org/10.18632/aging.101252>
15. , Y., Li, L., Fan, L. H., Jing, Y., Li, J., Ouyang, Y. C., Wang, Z. B., Hou, Y., Sun, Q. Y. (2019) N-acetyl-L-cysteine (NAC) delays post-ovulatory oocyte aging in mouse. Aging (Albany NY) 11, 2020-2030.
<https://doi.org/10.18632/aging.101898>
16. , J., Zhang, J., Li, H., Wang, T. Y., Zhang, C. X., Luo, M. J., Tan, J. H. (2015) Cumulus cells accelerate oocyte aging by releasing soluble Fas ligand in mice. Sci. Rep. 5, 8683.
<https://doi.org/10.1038/srep08683>
