Yamauchi Kaori, Hasegawa Kouichi, Chuma Shinichiro, Nakatsuji Norio, Suemori Hirofumi
Laboratory of Embryonic Stem Cell Research, Stem Cell Research Center, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan.
PLoS One. 2009;4(4):e5338. doi: 10.1371/journal.pone.0005338. Epub 2009 Apr 28.
Mouse embryonic stem (ES) cells can differentiate into female and male germ cells in vitro. Primate ES cells can also differentiate into immature germ cells in vitro. However, little is known about the differentiation markers and culture conditions for in vitro germ cell differentiation from ES cells in primates. Monkey ES cells are thus considered to be a useful model to study primate gametogenesis in vitro. Therefore, in order to obtain further information on germ cell differentiation from primate ES cells, this study examined the ability of cynomolgus monkey ES cells to differentiate into germ cells in vitro.
To explore the differentiation markers for detecting germ cells differentiated from ES cells, the expression of various germ cell marker genes was examined in tissues and ES cells of the cynomolgus monkey (Macaca fascicularis). VASA is a valuable gene for the detection of germ cells differentiated from ES cells. An increase of VASA expression was observed when differentiation was induced in ES cells via embryoid body (EB) formation. In addition, the expression of other germ cell markers, such as NANOS and PIWIL1 genes, was also up-regulated as the EB differentiation progressed. Immunocytochemistry identified the cells expressing stage-specific embryonic antigen (SSEA) 1, OCT-4, and VASA proteins in the EBs. These cells were detected in the peripheral region of the EBs as specific cell populations, such as SSEA1-positive, OCT-4-positive cells, OCT-4-positive, VASA-positive cells, and OCT-4-negative, VASA-positive cells. Thereafter, the effect of mouse gonadal cell-conditioned medium and growth factors on germ cell differentiation from monkey ES cells was examined, and this revealed that the addition of BMP4 to differentiating ES cells increased the expression of SCP1, a meiotic marker gene.
VASA is a valuable gene for the detection of germ cells differentiated from ES cells in monkeys, and the identification and characterization of germ cells derived from ES cells are possible by using reported germ cell markers in vivo, including SSEA1, OCT-4, and VASA, in vitro as well as in vivo. These findings are thus considered to help elucidate the germ cell developmental process in primates.
小鼠胚胎干细胞(ES细胞)可在体外分化为雌性和雄性生殖细胞。灵长类ES细胞也能在体外分化为未成熟生殖细胞。然而,关于灵长类动物ES细胞体外分化为生殖细胞的分化标志物和培养条件,人们了解甚少。因此,猴ES细胞被认为是研究灵长类动物体外配子发生的有用模型。所以,为了获取更多关于灵长类动物ES细胞分化为生殖细胞的信息,本研究检测了食蟹猴ES细胞在体外分化为生殖细胞的能力。
为探究检测ES细胞分化产生的生殖细胞的分化标志物,检测了食蟹猴(猕猴)组织和ES细胞中各种生殖细胞标志物基因的表达。VASA是检测ES细胞分化产生的生殖细胞的一个重要基因。当通过胚状体(EB)形成诱导ES细胞分化时,观察到VASA表达增加。此外,随着EB分化的进行,其他生殖细胞标志物如NANOS和PIWIL1基因的表达也上调。免疫细胞化学鉴定出EB中表达阶段特异性胚胎抗原(SSEA)1、OCT-4和VASA蛋白的细胞。这些细胞在EB的周边区域被检测到,为特定细胞群体,如SSEA1阳性、OCT-4阳性细胞,OCT-4阳性、VASA阳性细胞,以及OCT-4阴性、VASA阳性细胞。此后,检测了小鼠性腺细胞条件培养基和生长因子对猴ES细胞生殖细胞分化的影响,结果显示向分化的ES细胞中添加BMP4可增加减数分裂标志物基因SCP1的表达。
VASA是检测猴ES细胞分化产生的生殖细胞的一个重要基因,利用体内外已报道的生殖细胞标志物,包括SSEA1、OCT-4和VASA,对ES细胞来源的生殖细胞进行鉴定和特性分析是可行的。因此,这些发现被认为有助于阐明灵长类动物生殖细胞的发育过程。