Alterations in mitochondrial membrane potential during preimplantation stages of mouse and human embryo development

被引:177
作者
Acton, BM
Jurisicova, A
Jurisica, I
Casper, RF
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Dept Physiol, Toronto, ON M5G 1X5, Canada
[2] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Dept Obstet & Gynecol, Div Reprod Sci, Toronto, ON M5G 1X5, Canada
[3] Univ Toronto, Ontario Canc Inst, Princess Margaret Hosp, Univ Hlth Network,Dept Comp Sci,Div Canc Informat, Toronto, ON, Canada
[4] Univ Toronto, Ontario Canc Inst, Princess Margaret Hosp,Dept Med Biophys, Univ Hlth Network,Div Canc Informat, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
embryo; fragmentation; IVF; mitochondria; mitochondrial membrane potential;
D O I
10.1093/molehr/gah004
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mitochondria are cellular organelles regulating metabolism and cell death pathways. This study examined changes in mitochondrial membrane potential (DeltaPsim) throughout the stages of preimplantation development in mouse embryos conceived either in vivo or in vitro and human embryos donated to research from IVF. Embryos stained with the DeltaPsim-sensitive dye (JC-1) were quantified for the ratio of high- to low-polarized mitochondria using a deconvolution microscope. Overall, mouse zygotes and early embryos contain a subset of high-polarized mitochondria with a progressive increase in the ratio of DeltaPsim observed with increasing cleavage. A transient increase in the ratio of high to low DeltaPsim was observed in in vivo fertilized 2-cell stage embryos, coincident with embryonic genome activation in the mouse, but not in 2-cell embryos obtained through IVF. We further observed that arrested mouse 2-cell embryos possessed an increased ratio of DeltaPsim compared with non-arrested embryos. In human 8-cell embryos we observed an increased ratio of high- to low-polarized mitochondria with increasing degrees of embryo fragmentation. We concluded that the pattern of mitochondrial membrane potential progressively changes throughout preimplantation development, and that an aberrant shift in DeltaPsim could contribute to, or is associated with, decreased developmental potential.
引用
收藏
页码:23 / 32
页数:10
相关论文
共 65 条
[1]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[2]   PATTERNS OF ORGANELLE DISTRIBUTION IN MOUSE EMBRYOS DURING PREIMPLANTATION DEVELOPMENT [J].
BATTEN, BE ;
ALBERTINI, DF ;
DUCIBELLA, T .
AMERICAN JOURNAL OF ANATOMY, 1987, 178 (02) :204-213
[3]  
Bavister B D, 2000, Hum Reprod, V15 Suppl 2, P189
[4]   PATTERN OF ENERGY METABOLISM IN MOUSE OOCYTE AND ZYGOTE [J].
BIGGERS, JD ;
WHITTING.DG ;
DONAHUE, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 58 (02) :560-&
[5]   DEVELOPMENT OF SPARE HUMAN PREIMPLANTATION EMBRYOS INVITRO - AN ANALYSIS OF THE CORRELATIONS AMONG GROSS MORPHOLOGY, CLEAVAGE RATES, AND DEVELOPMENT TO THE BLASTOCYST [J].
BOLTON, VN ;
HAWES, SM ;
TAYLOR, CT ;
PARSONS, JH .
JOURNAL OF IN VITRO FERTILIZATION AND EMBRYO TRANSFER, 1989, 6 (01) :30-35
[6]   HUMAN-GENE EXPRESSION 1ST OCCURS BETWEEN THE 4-CELL AND 8-CELL STAGES OF PREIMPLANTATION DEVELOPMENT [J].
BRAUDE, P ;
BOLTON, V ;
MOORE, S .
NATURE, 1988, 332 (6163) :459-461
[7]   Mitochondrial DNA heteroplasmy after human ooplasmic transplantation [J].
Brenner, CA ;
Barritt, JA ;
Willadsen, S ;
Cohen, J .
FERTILITY AND STERILITY, 2000, 74 (03) :573-578
[8]   Ooplasmic transfer in mature human oocytes [J].
Cohen, J ;
Scott, R ;
Alikani, M ;
Schimmel, T ;
Munne, S ;
Levron, J ;
Wu, L ;
Brenner, C ;
Warner, C ;
Willadsen, S .
MOLECULAR HUMAN REPRODUCTION, 1998, 4 (03) :269-280
[9]   Mouse offspring after microinjection of heated spermatozoa [J].
Cozzi, J ;
Monier-Gavelle, F ;
Lièvre, N ;
Bomsel, M ;
Wolf, JP .
BIOLOGY OF REPRODUCTION, 2001, 65 (05) :1518-1521
[10]   Mitochondrial DNA in mammalian reproduction [J].
Cummins, J .
REVIEWS OF REPRODUCTION, 1998, 3 (03) :172-182