Mitochondrial networks of cumulus cells and oocyte quality
- Authors: Panferov E.V.1, Tapilskaya N.I.2, Masieva K.S.3, Ob’edkova K.V.2, Gzgzyan A.M.2
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Affiliations:
- Institute of Cytology Russian Academy of Science
- Ott Research Institute of Obstetrics, Gynecology and Reproductology
- Military Medical Academy
- Issue: Vol 41, No 3 (2022)
- Pages: 303-308
- Section: Original articles
- URL: https://journal-vniispk.ru/RMMArep/article/view/109074
- DOI: https://doi.org/10.17816/rmmar109074
- ID: 109074
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Abstract
BACKGROUND: Mitochondria play vital roles in oocyte functions and they are critical indicators of oocyte quality which is important for fertilization and development into viable offspring. Quality-compromised oocytes in which mitochondrial dysfunction plays a significant role are correlated with infertility, developmental disorders and embryo loss. A significant role in the oocytes of cytoplasmic accumulation and a sufficient amount of the mitochondrial pool of oocytes is played by the cumulus cells surrounding it.
AIM: to conduct a comparative analysis between the state of mitochondrial networks of cumulus cells and the quality of oocytes.
MATERIALS AND METHODS: The study included 22 women aged 28 to 37 years inclusive (mean age 32.3 ± 1.2 years) with tubal infertility. During the assisted reproductive technology procedures, 74 oocytes were obtained. 39 good quality oocytes and their cumulus cells were compared with 35 bad quality oocytes and their cumulus cells respectively. After puncture of ovarian follicles cumulus cells were isolated and stained with fluorescent dye for cell tracing and mitochondrial imaging in vivo. The method of confocal microscopy was used to analyze the three-dimensional organization of mitochondria in 20–30 cells of one pool of follicular fluid. The following parameters were used to evaluate the mitochondrial network: fluorescence decay time and fluorescence intensity.
RESULTS: The decay time of fluorescence in cumulus cells associated with a good quality oocyte was significantly higher (p = 0.032) than in the case of identification of oocytes with negative signs.
CONCLUSION: The structure of mitochondrial networks in cumulus cells correlates (r = 0.76) with the quality of oocytes.
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##article.viewOnOriginalSite##About the authors
Egor V. Panferov
Institute of Cytology Russian Academy of Science
Email: panferov.aux@gmail.com
master of the Institute of cytology of the Russian Academy of Sciences
Russian Federation, Saint PetersburgNatalya I. Tapilskaya
Ott Research Institute of Obstetrics, Gynecology and Reproductology
Author for correspondence.
Email: tapnatalia@yandex.ru
ORCID iD: 0000-0001-5309-0087
SPIN-code: 3605-0413
Scopus Author ID: 23013489000
ResearcherId: A-7504-2016
M.D., D.Sc. (Medicine), Professor, leading research scientist
Russian Federation, Saint PetersburgKristina S. Masieva
Military Medical Academy
Email: masieva98@mail.ru
6th year student
Russian Federation, Saint PetersburgKseniya V. Ob’edkova
Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: obedkova_ks@mail.ru
ORCID iD: 0000-0002-2056-7907
SPIN-code: 2709-2890
M.D., Ph.D. (Medicine), research scientist of the Reproduction Department
Russian Federation, Saint PetersburgAlexander M. Gzgzyan
Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: iagmail@ott.ru
ORCID iD: 0000-0003-3917-9493
SPIN-code: 6412-4801
Scopus Author ID: 56232643300
M.D., D.Sc. (Medicine), Head of the Reproduction Department
Russian Federation, Saint PetersburgReferences
- Park SU, Walsh L, Berkowitz KM. Mechanisms of ovarian aging. Reproduction. 2021;162(2): R19–R33. doi: 10.1530/REP-21-0022
- Duckney PJ, Wang P, Hussey PJ. Membrane contact sites and cytoskeleton-membrane interactions in autophagy. FEBS Lett. 2022;596:2093-2103. doi: 10.1002/1873-3468.14414
- Quinlan CL, Perevoshchikova IV, Hey-Mogensen M, et al. Sites of reactive oxygen species generation by mitochondria oxidizing different substrates. Redox biology. 2013;1(1):304–312. doi: 10.1016/j.redox.2013.04.005
- Murphy MP. Mitochondrial thiols in antioxidant protection and redox signaling: distinct roles for glutathionylation and other thiol modifications. Antioxidants & redox signaling. 2012;16(6):476–495. doi: 10.1089/ars.2011.4289
- von Mengden L, Klamt F, Smitz J. Redox biology of human cumulus cells: basic concepts, impact on oocyte quality, and potential clinical use. Antioxidants & redox signaling. 2020;32(8):522–535. doi: 10.1089/ars.2019.7984
- Richani D, Dunning KR, Thompson JG, et al. Metabolic co-dependence of the oocyte and cumulus cells: essential role in determining oocyte developmental competence. Human reproduction update. 2021;27(1):27–47. doi: 10.1093/humupd/dmaa043
- Friedman JR, Nunnari J. Mitochondrial form and function. Nature. 2014;505(7483):335–343. doi: 10.1038/nature12985
- Schofield JH, Schafer ZT. Mitochondrial reactive oxygen species and mitophagy: a complex and nuanced relationship. Antioxidants & redox signaling. 2021;34(7):517–530. doi: 10.1089/ars.2020.8058
- Ikonomi N, Werle SD, Schwab JD, Kestler HA. Discrete Logic modeling of cell signaling pathways. Methods Mol Biol. 2022;2488:159–181. doi: 10.1007/978-1-0716-2277-3_12
- Rodríguez-Varela C, Labarta E. Role of mitochondria transfer in infertility: A Commentary. Cells. 2022.;11(12):1867. doi: 10.3390/cells11121867
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