The role of mitochondrial activity in female fertility and assisted reproductive technologies: overview and current insights

被引:90
作者
Cecchino, Gustavo Nardini [1 ,2 ,3 ]
Seli, Emre [4 ]
Alves da Motta, Eduardo Leme [1 ,5 ]
Antonio Garcia-Velasco, Juan [2 ,3 ]
机构
[1] Univ Fed Sao Paulo, Dept Gynecol, Rua Napoleao de Barros 632, BR-04024002 Sao Paulo, SP, Brazil
[2] Rey Juan Carlos Univ, Dept Gynecol & Obstet, Ave Atenas S-N, Madrid 28922, Spain
[3] Valencian Infertil Inst IVI, Ave Talgo 68, Madrid 28023, Spain
[4] Yale Sch Med, Dept Obstet Gynecol & Reprod Sci, 310 Cedar St,LSOG 304B, New Haven, CT 06520 USA
[5] Huntington Reprod Med, Ave Republ Libano 529, BR-04501000 Sao Paulo, SP, Brazil
关键词
ART; Assisted reproductive technologies; Infertility; Mitochondria; Oocyte; CONTROLLED OVARIAN STIMULATION; IN-VITRO FERTILIZATION; DNA COPY NUMBER; OXIDATIVE STRESS; CUMULUS CELLS; OOCYTE QUALITY; PATERNAL MITOCHONDRIA; REPLACEMENT THERAPY; FOLLICULAR-FLUID; SPINDLE TRANSFER;
D O I
10.1016/j.rbmo.2018.02.007
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Mitochondria have been implicated as key factors regulating female reproductive processes. Notable progress has been made in determining the role of mitochondria with respect to oocyte maturation, fertilization and early embryo development. In addition, mitochondrial function and dysfunction has been the subject of various studies in ovarian ageing and metabolic stress models. However, the overall mitochondrial impact on female fertility is yet to be uncovered. The mitochondrial DNA content of granulosa, cumulus and trophectoderm cells is being explored as a biomarker of oocyte quality and embryo viability. As growing evidence suggests that embryo potential could be related to the ability of oocyte mitochondria to generate energy, efforts have been made to investigate the possibility of improving mitochondrial capacity in women with poor outcomes after treatment with assisted reproductive technologies. Thus far, therapeutic attempts have focused mainly on using nutrients to restore mitochondrial function and transferring mitochondria from autologous germline precursor cells. Moreover, new perspectives on optimizing infertility treatments have arisen with modern mitochondrial replacement therapies, which are being applied in women with mitochondrial disease-causing mutations. This review explores aspects of the distinctive contribution of mitochondria to reproductive processes and discusses current and emerging clinical implications. (C) 2018 Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:686 / 697
页数:12
相关论文
共 149 条
[1]   CoQ10 increases mitochondrial mass and polarization, ATP and Oct4 potency levels, and bovine oocyte MII during IVM while decreasing AMPK activity and oocyte death [J].
Abdulhasan, M. K. ;
Li, Q. ;
Dai, J. ;
Abu-Soud, H. M. ;
Puscheck, E. E. ;
Rappolee, D. A. .
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2017, 34 (12) :1595-1607
[2]   Oxidative stress in an assisted reproductive techniques setting [J].
Agarwal, Ashok ;
Said, Tamer M. ;
Bedaiwy, Mohamed A. ;
Banerjee, Jashoman ;
Alvarez, Juan G. .
FERTILITY AND STERILITY, 2006, 86 (03) :503-512
[3]   Utility of antioxidants during assisted reproductive techniques: an evidence based review [J].
Agarwal, Ashok ;
Durairajanayagam, Damayanthi ;
du Plessis, Stefan S. .
REPRODUCTIVE BIOLOGY AND ENDOCRINOLOGY, 2014, 12
[4]   First birth following spindle transfer for mitochondrial replacement therapy: hope and trepidation [J].
Alikani, Mina ;
Fauser, Bart C. J. ;
Garcia-Valesco, Juan Antonio ;
Simpson, Joe Leigh ;
Johnson, Martin H. .
REPRODUCTIVE BIOMEDICINE ONLINE, 2017, 34 (04) :333-336
[5]   Reproductive aging is associated with changes in oocyte mitochondrial dynamics, function, and mtDNA quantity [J].
Babayev, Elnur ;
Wang, Tianren ;
Szigeti-Buck, Klara ;
Lowther, Katie ;
Taylor, Hugh S. ;
Horvath, Tamas ;
Seli, Emre .
MATURITAS, 2016, 93 :121-130
[6]   Gonadotropin dose is negatively correlated with live birth rate: analysis of more than 650,000 assisted reproductive technology cycles [J].
Baker, Valerie L. ;
Brown, Morton B. ;
Luke, Barbara ;
Smith, George W. ;
Ireland, James J. .
FERTILITY AND STERILITY, 2015, 104 (05) :1145-+
[7]   Mitochondria, oxidants, and aging [J].
Balaban, RS ;
Nemoto, S ;
Finkel, T .
CELL, 2005, 120 (04) :483-495
[8]   Epigenetic and experimental modifications in early mammalian development: Part II - Cytoplasmic transfer in assisted reproduction [J].
Barritt, JA ;
Willadsen, S ;
Brenner, C ;
Cohen, J .
HUMAN REPRODUCTION UPDATE, 2001, 7 (04) :428-435
[9]   Mitochondria in human offspring derived from ooplasmic transplantation [J].
Barritt, JA ;
Brenner, CA ;
Malter, HE ;
Cohen, J .
HUMAN REPRODUCTION, 2001, 16 (03) :513-516
[10]  
Barritt Jason A, 2001, Reprod Biomed Online, V3, P47, DOI 10.1016/S1472-6483(10)61966-9