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Mitochondrial macro-haplogroup JT may play a protective role in ovarian ageing.线粒体宏单倍群JT可能在卵巢衰老中发挥保护作用。
Mitochondrion. 2014 Sep;18:1-6. doi: 10.1016/j.mito.2014.08.002. Epub 2014 Aug 14.
2
The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.线粒体DNA 10197 G>A突变导致伴有急性听觉失认症的MELAS/Leigh重叠综合征。
Mitochondrial DNA. 2015 Apr;26(2):208-12. doi: 10.3109/19401736.2014.905860. Epub 2014 Apr 8.
3
Contributions of the actin cytoskeleton to the emergence of polarity during maturation in human oocytes.在人类卵母细胞成熟过程中,肌动蛋白细胞骨架对极性出现的贡献。
Mol Hum Reprod. 2014 Mar;20(3):200-7. doi: 10.1093/molehr/gat085. Epub 2013 Nov 20.
4
The immature human ovary shows loss of abnormal follicles and increasing follicle developmental competence through childhood and adolescence.在儿童期和青春期,未成熟的人类卵巢中异常卵泡逐渐减少,卵泡发育能力不断增强。
Hum Reprod. 2014 Jan;29(1):97-106. doi: 10.1093/humrep/det388. Epub 2013 Oct 17.
5
Mechanistic foundations of the metaphase II spindle of human oocytes matured in vivo and in vitro.体内和体外成熟的人卵母细胞中期 II 纺锤体的机制基础。
Hum Reprod. 2013 Dec;28(12):3271-82. doi: 10.1093/humrep/det381. Epub 2013 Oct 15.
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Germline mitochondrial DNA mutations aggravate ageing and can impair brain development.胚系线粒体 DNA 突变会加重衰老,并可能损害大脑发育。
Nature. 2013 Sep 19;501(7467):412-5. doi: 10.1038/nature12474. Epub 2013 Aug 21.
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Reproductive aging is associated with decreased mitochondrial abundance and altered structure in murine oocytes.生殖衰老与卵母细胞中线粒体数量减少和结构改变有关。
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8
Prevention of mitochondrial disease inheritance by assisted reproductive technologies: prospects and challenges.通过辅助生殖技术预防线粒体疾病遗传:前景与挑战
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Meiotic origins of maternal age-related aneuploidy.母龄相关非整倍体的减数分裂起源。
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10
Pathogenic mitochondrial DNA mutations are common in the general population.致病性线粒体DNA突变在普通人群中很常见。
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重新审视生发泡移植作为卵巢储备功能减退的不孕女性非整倍体的一种治疗方法。

Revisiting germinal vesicle transfer as a treatment for aneuploidy in infertile women with diminished ovarian reserve.

作者信息

Zhang John

机构信息

Reproductive Endocrinology and Infertility, New Hope Fertility Center, 4 Columbus Circle, New York, NY, USA,

出版信息

J Assist Reprod Genet. 2015 Feb;32(2):313-7. doi: 10.1007/s10815-014-0400-3. Epub 2014 Dec 18.

DOI:10.1007/s10815-014-0400-3
PMID:25515532
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4354183/
Abstract

The maturation and meiotic competence of human oocyte requires both healthy cytoplasmic and nuclear compartments. Germinal vesicle (GV) transfer techniques have represented useful tools for studying the interaction between the nucleus and the cytoplasm in oocyte maturation process in mammals. This report summarizes an update on the recent findings on GV transfer pertaining to improving meiotic resumption and ability of immature oocytes to mature. It also addresses mitochondrial DNA heteroplasmy as a challenge in GV transfer technology. Altogether, data to date indicate that GV transfer could improve the quality of human oocytes especially in women with advanced maternal age who usually have high rates of spindle abnormality and chromosomal misalignment. Although experimental, this technique represents a viable therapeutic option for women with diminished ovarian reserve who do not produce mature oocytes or good embryos during IVF treatment.

摘要

人类卵母细胞的成熟和减数分裂能力需要健康的细胞质和细胞核区域。生发泡(GV)移植技术已成为研究哺乳动物卵母细胞成熟过程中细胞核与细胞质之间相互作用的有用工具。本报告总结了有关GV移植在改善减数分裂恢复和未成熟卵母细胞成熟能力方面的最新研究结果。它还讨论了线粒体DNA异质性这一GV移植技术面临的挑战。迄今为止的数据表明,GV移植可以提高人类卵母细胞的质量,尤其是对于高龄产妇,她们通常纺锤体异常和染色体排列错误的发生率较高。尽管是实验性的,但这项技术对于卵巢储备功能减退、在体外受精治疗期间无法产生成熟卵母细胞或优质胚胎的女性而言,是一种可行的治疗选择。