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食蟹猴原始生殖细胞的采集与培养()。

Collection and culture of primordial germ cells from cynomolgus monkeys ().

作者信息

Okada Hironori, Hatori Masanori, Shimozawa Nobuhiro, Tsuchiya Hideaki, Kuwana Takashi, Sankai Tadashi

机构信息

Tsukuba Primate Research Center, National Institute of Biomedical Innovation.

Graduate School of Comprehensive Human Sciences, University of Tsukuba.

出版信息

Reprod Med Biol. 2007 Nov 7;6(4):203-210. doi: 10.1111/j.1447-0578.2007.00186.x. eCollection 2007 Dec.

Abstract

To clarify the location of primordial germ cells (PGC) in an embryo of target-age and to examine the culture environment of the PCG. The days of ovulation and fertilization were estimated by measuring the serum concentration of estrogen. Pregnancy was confirmed by measurement of the serum concentration of the beta subunit of macaque chorionic gonadotropin and by ultrasonography. We also examined the location of PGC in the embryo at the time of retrieval. Results showed that PGC in an embryo were in the hindguts at day 30 postfertilization, arrived at the genital ridges via mesenteries at approximately day 33 postfertilization, and colonized the gonads by day 36 postfertilization. In conclusion, embryos collected on day 33 postfertilization are more suitable for obtaining PGC from cynomolgus monkeys. The PGC collected from cynomolgus monkey fetuses were cultured under conditions for the derivation and culture of human embryonic germ cells; enzymatically dispersed single cells were cultured on a SIM thioguanine-resistant ouabain-resistant cells (STO) feeder layer with recombinant human leukemia inhibitory factor, recombinant human basic fibroblast growth factor and forskolin. The cells from genital ridges and mesenteries at day 33 postfertilization had alkaline phosphatase (ALP) activity for a maximum of 13 days. In contrast, ALP activity had been held for 2 months under the same culture condition when the cells were derived from the gonads at day 66 postfertilization. Derivation of an embryonic germ cell from a cynomolgus monkey was not achieved from these cultures. (Reprod Med Biol 2007; : 203-210).

摘要

为明确目标年龄胚胎中原始生殖细胞(PGC)的位置,并检测PGC的培养环境。通过检测血清雌激素浓度估算排卵和受精日期。通过检测猕猴绒毛膜促性腺激素β亚基的血清浓度及超声检查确认妊娠。我们还检查了取材时胚胎中PGC的位置。结果显示,受精后30天时胚胎中的PGC位于后肠,受精后约33天时经肠系膜到达生殖嵴,受精后36天时定殖于性腺。总之,受精后33天收集的胚胎更适合从食蟹猴获取PGC。将从食蟹猴胎儿收集的PGC在人胚胎生殖细胞的分离和培养条件下培养;酶消化分散的单细胞在含重组人白血病抑制因子、重组人碱性成纤维细胞生长因子和福斯可林的SIM硫代鸟嘌呤抗性哇巴因抗性细胞(STO)饲养层上培养。受精后33天来自生殖嵴和肠系膜处的细胞碱性磷酸酶(ALP)活性最多持续13天。相比之下,当细胞来自受精后66天的性腺时,在相同培养条件下ALP活性可维持2个月。从这些培养物中未实现食蟹猴胚胎生殖细胞的分离。(《生殖医学与生物学》2007年;:203 - 210)

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