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野生山羊-兔核移植胚胎的体外培养及线粒体DNA命运

In vitro culture and mtDNA fate of ibex-rabbit nuclear transfer embryos.

作者信息

Jiang Yan, Chen Tao, Nan Chang-Long, Ouyang Ying-Chun, Sun Qing-Yuan, Chen Da-Yuan

机构信息

State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.

出版信息

Zygote. 2005 Aug;13(3):233-40. doi: 10.1017/s0967199405003254.

Abstract

Rabbit oocyte can be used as the recipient in interspecies somatic cell nuclear transfer (iSCNT). This work was undertaken in order to study the developmental competence of Capra ibex somatic cells reprogrammed by rabbit oocytes and the fate of mitochondria in iSCNT embryos. Metaphase II (MII) oocytes from superovulated rabbit were used as nuclear recipients. The nuclear donors were Capra ibex somatic cells with different proliferative status: population doubling time (PDL) = 15 +/- 2 (group 1), 35 +/- 2 (group 2), 55 +/- 2 (group 3) and 70 +/- 2 (group 4). Oocytes reconstructed with electrical pulses (2.1kV/cm, 10 micros, 2 times) were activated (1.4kV, 20 micros, 2 times) and then cultured in Medium199 containing 10% fetal bovine serum at 38.5 degrees C, 5% CO2 in air. In groups 1, 2, 3 and 4, the fusion rates were 35.83%, 66.03%, 65.40% and 35.35%, respectively. Similar cleavage rates were observed among the four groups. However, the developmental potential to morula/blastocyst from early nuclear donor embryos (16.42%/10.45%) was significantly higher (p < 0.05) than in terminal donor embryos (9.52%/3.81%). Polymerase chain reaction analysis of the mitochondrial (mt) DNA cytb gene demonstrated that mtDNAs from ibex and rabbit could be detected at various developmental stages before implantation. In conclusion, our results provide some original information about rescuing Capra ibex using the iSCNT technique. These results indicate that: (1) enucleated rabbit oocytes make Capra ibex fibroblast nuclei reprogramme; (2) the proliferative status of donor cells affects the efficiency of iSCNT; and (3) rabbit ooplasm rescues the donor-derived mtDNAs, resulting in mtDNA heteroplasmy before implantation.

摘要

兔卵母细胞可作为种间体细胞核移植(iSCNT)的受体。开展本研究是为了探究经兔卵母细胞重编程的北山羊体细胞的发育能力以及iSCNT胚胎中线粒体的命运。将超排兔的中期Ⅱ(MⅡ)卵母细胞用作核受体。核供体为处于不同增殖状态的北山羊体细胞:群体倍增时间(PDL)= 15±2(第1组)、35±2(第2组)、55±2(第3组)和70±2(第4组)。用电脉冲(2.1kV/cm,10微秒,2次)重构的卵母细胞经激活(1.4kV,20微秒,2次)后,置于含10%胎牛血清的M199培养基中,于38.5℃、5%二氧化碳的空气环境中培养。在第1、2、3和4组中,融合率分别为35.83%、66.03%、65.40%和35.35%。四组的卵裂率相近。然而,早期核供体胚胎发育至桑葚胚/囊胚的潜力(16.42%/10.45%)显著高于晚期供体胚胎(9.52%/3.81%)(p < 0.05)。线粒体(mt)DNA细胞色素b基因的聚合酶链反应分析表明,在植入前的各个发育阶段均可检测到来自北山羊和兔的mtDNA。总之,我们的结果为利用iSCNT技术拯救北山羊提供了一些原始信息。这些结果表明:(1)去核兔卵母细胞使北山羊成纤维细胞核重编程;(2)供体细胞的增殖状态影响iSCNT效率;(3)兔卵细胞质拯救了供体来源的mtDNA,导致植入前mtDNA异质性。

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