Non-invasive imaging of human embryos before embryonic genome activation predicts development to the blastocyst stage

被引:584
作者
Wong, Connie C. [1 ,2 ]
Loewke, Kevin E. [1 ,2 ,3 ]
Bossert, Nancy L. [4 ]
Behr, Barry [2 ]
De Jonge, Christopher J. [4 ]
Baer, Thomas M. [5 ]
Pera, Renee A. Reijo [1 ,2 ]
机构
[1] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Obstet & Gynecol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[4] Univ Minnesota, Reprod Med Ctr, Minneapolis, MN USA
[5] Stanford Univ, Dept Appl Phys, Stanford Photon Res Ctr, Stanford, CA 94305 USA
关键词
HUMAN PREIMPLANTATION EMBRYOS; CELL-FATE DECISIONS; GENE-EXPRESSION; ASSISTED REPRODUCTION; TIME; CLEAVAGE; QUALITY; RATES; PREGNANCY; RNA;
D O I
10.1038/nbt.1686
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We report studies of preimplantation human embryo development that correlate time-lapse image analysis and gene expression profiling. By examining a large set of zygotes from in vitro fertilization (IVF), we find that success in progression to the blastocyst stage can be predicted with >93% sensitivity and specificity by measuring three dynamic, noninvasive imaging parameters by day 2 after fertilization, before embryonic genome activation (EGA). These parameters can be reliably monitored by automated image analysis, confirming that successful development follows a set of carefully orchestrated and predictable events. Moreover, we show that imaging phenotypes reflect molecular programs of the embryo and of individual blastomeres. Single-cell gene expression analysis reveals that blastomeres develop cell autonomously, with some cells advancing to EGA and others arresting. These studies indicate that success and failure in human embryo development is largely determined before EGA. Our methods and algorithms may provide an approach for early diagnosis of embryo potential in assisted reproduction.
引用
收藏
页码:1115 / U199
页数:10
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