Department of Bioscience and Biotechnology, Bio-Organ Research Center/Animal Resources Research Center, Konkuk University, Hwayang-dong, Gwangjin-Gu, Seoul 143701, South Korea.
Exp Cell Res. 2010 Mar 10;316(5):747-61. doi: 10.1016/j.yexcr.2009.11.021. Epub 2009 Dec 7.
This study evaluated the essentiality of glial cell line-derived neurotrophic factor (GDNF) for in vitro culture of established mouse multipotent adult germline stem (maGS) cell lines by culturing them in the presence of GDNF, leukemia inhibitory factor (LIF) or both. We show that, in the absence of LIF, GDNF slows the proliferation of maGS cells and result in smaller sized colonies without any change in distribution of cells to different cell-cycle stages, expression of pluripotency genes and in vitro differentiation potential. Furthermore, in the absence of LIF, GDNF increased the expression of male germ-line genes and repopulated the empty seminiferous tubule of W/W(v) mutant mouse without the formation of teratoma. GDNF also altered the genomic imprinting of Igf2, Peg1, and H19 genes but had no effect on DNA methylation of Oct4, Nanog and Stra8 genes. However, these effects of GDNF were masked in the presence of LIF. GDNF also did not interfere with the multipotency of maGS cells if they are cultured in the presence of LIF. In conclusion, our results suggest that, in the absence of LIF, GDNF alters the growth characteristics of maGS cells and partially impart them some of the germline stem (GS) cell-like characteristics.
本研究评估了胶质细胞源性神经营养因子(GDNF)在体外培养已建立的小鼠多能成体生殖系干细胞(maGS)系中的必要性,方法是在存在 GDNF、白血病抑制因子(LIF)或两者的情况下培养它们。我们表明,在没有 LIF 的情况下,GDNF 会减缓 maGS 细胞的增殖,并导致细胞集落变小,而不会改变细胞在不同细胞周期阶段的分布、多能性基因的表达和体外分化潜能。此外,在没有 LIF 的情况下,GDNF 增加了雄性生殖系基因的表达,并在没有形成畸胎瘤的情况下重新填充 W/W(v) 突变小鼠的空生精小管。GDNF 还改变了 Igf2、Peg1 和 H19 基因的基因组印记,但对 Oct4、Nanog 和 Stra8 基因的 DNA 甲基化没有影响。然而,在存在 LIF 的情况下,GDNF 的这些作用被掩盖了。如果 maGS 细胞在存在 LIF 的情况下培养,GDNF 也不会干扰它们的多能性。总之,我们的结果表明,在没有 LIF 的情况下,GDNF 改变了 maGS 细胞的生长特性,并使它们具有部分生殖系干细胞(GS)细胞样特征。