Naito Mitsuru, Harumi Takashi, Kuwana Takashi
National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.
National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.
Anim Reprod Sci. 2015 Feb;153:50-61. doi: 10.1016/j.anireprosci.2014.12.003. Epub 2014 Dec 24.
Production of germline chimaeric chickens by the transfer of cultured primordial germ cells (PGC) is a useful system for germline manipulation. A novel culture system was developed for chicken PGC isolated from embryonic blood. The isolated PGC were cultured on feeder cells derived from chicken embryonic fibroblast. The cultured PGC formed colonies and they proliferated about 300-times during the first 30 days. The cultured PGC retained the ability to migrate to recipient gonads and were also chicken VASA homologue (CVH)-positive. Female PGC were present in the mixed-sex PGC populations cultured for more than 90 days and gave rise to viable offspring efficiently via germline chimaeric chickens. Male cultured PGC were transferred to recipient embryos and produced putative chimaeric chickens. The DNA derived from the cultured PGC was detected in the sperm samples of male putative chimaeric chickens, but no donor derived offspring were obtained. Donor-derived offspring were also obtained from germline chimaeric chickens by the transfer of frozen-thawed cultured PGC. The culture method for PGC developed in the present study is useful for manipulation of the germline in chickens, such as preservation of genetic resources and gene transfer.
通过转移培养的原始生殖细胞(PGC)来生产种系嵌合鸡是一种用于种系操作的有用系统。针对从胚胎血液中分离出的鸡PGC,开发了一种新型培养系统。分离出的PGC在源自鸡胚胎成纤维细胞的饲养细胞上进行培养。培养的PGC形成集落,并且在最初30天内增殖了约300倍。培养的PGC保留了迁移到受体性腺的能力,并且也是鸡VASA同源物(CVH)阳性。雌性PGC存在于培养超过90天的混合性别的PGC群体中,并通过种系嵌合鸡有效地产生了可存活的后代。将雄性培养的PGC转移到受体胚胎中,产生了推定的嵌合鸡。在雄性推定嵌合鸡的精子样本中检测到了源自培养PGC的DNA,但未获得供体来源的后代。通过转移冻融的培养PGC,也从种系嵌合鸡中获得了供体来源的后代。本研究中开发的PGC培养方法对于鸡的种系操作,如遗传资源保存和基因转移是有用的。