Li Pei-Zhen, Yan Guang-Yao, Han Le, Pang Jing, Zhong Bu-Shuai, Zhang Guo-Min, Wang Feng, Zhang Yan-Li
1 Jiangsu Livestock Embryo Engineering Laboratory, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, China.
Reprod Sci. 2017 Feb;24(2):300-312. doi: 10.1177/1933719116654990. Epub 2016 Sep 27.
Bone marrow mesenchymal stem cells (BMSCs), which are well characterized and widely utilized adult stem cells, encompass the capacity to commit to a variety of cell types. This study was conducted to develop an effective way to induce goat BMSCs (gBMSCs) to transdifferentiate toward putative male germ cells by overexpressing STRA8 (stimulated by RA-8), BOULE (also called BOLL), and DAZL (deleted in azoospermia-like). First, we found that the expression levels of these 3 genes gradually increased during development of the goat testis from 10 days postnatal to 8 months old. Therefore, we hypothesized that overexpressing these genes might contribute to the transdifferentiation of gBMSCs toward germ cells. We then overexpressed, separately and in combination, STRA8, BOULE, and DAZL in gBMSCs. Our results showed that a small population of transfected gBMSCs transdifferentiated into early goat germ cell-like cells and that these cells expressed primordial germ cell specification genes STELLA (also known as DPPA3, developmental pluripotency associated 3) and C-KIT (tyrosine kinase receptor) as well as premeiotic genes MVH (mouse vasa homolog), DAZL, BOULE, STRA8, PIWIL2 (piwi-like RNA-mediated gene silencing 2), and RNF17 (ring finger protein 17). Importantly, results from quantitative reverse transcription polymerase chain reaction, immunofluorescence, and Western blot analysis showed that the meiotic marker synaptonemal complex protein 3 (SCP3) significantly increased in transfected cells compared to untransfected control cells ( P < .05). Additionally, the co-overexpression group cells had the highest SCP3 messenger RNA and protein expression levels, which indicated that 3-gene co-overexpression had the highest potential to transdifferentiate gBMSCs to germ cells. Taken together, these results demonstrate that the overexpression of STRA8, BOULE, and DAZL was able to promote the transdifferentiation of gBMSCs to early goat germ cell-like cells in vitro, which probably enhanced maturation and progression through meiosis. This approach would be important to generating gametes for future basic science as well as for potential clinical applications.
骨髓间充质干细胞(BMSCs)是特征明确且广泛应用的成体干细胞,具有分化为多种细胞类型的能力。本研究旨在开发一种有效的方法,通过过表达STRA8(视黄酸刺激基因8)、BOULE(也称为BOLL)和DAZL(无精子症样缺失基因),诱导山羊骨髓间充质干细胞(gBMSCs)向假定的雄性生殖细胞转分化。首先,我们发现从出生后10天到8个月大的山羊睾丸发育过程中,这3个基因的表达水平逐渐升高。因此,我们推测过表达这些基因可能有助于gBMSCs向生殖细胞的转分化。然后,我们分别或联合在gBMSCs中过表达STRA8、BOULE和DAZL。我们的结果表明,一小部分转染的gBMSCs转分化为早期山羊生殖细胞样细胞,这些细胞表达原始生殖细胞特异性基因STELLA(也称为DPPA3,发育多能性相关蛋白3)和C-KIT(酪氨酸激酶受体)以及减数分裂前基因MVH(小鼠vasa同源物)、DAZL、BOULE、STRA8、PIWIL2(piwi样RNA介导的基因沉默蛋白2)和RNF17(环指蛋白17)。重要的是,定量逆转录聚合酶链反应、免疫荧光和蛋白质印迹分析结果表明,与未转染的对照细胞相比,转染细胞中的减数分裂标记联会复合体蛋白3(SCP3)显著增加(P <.05)。此外,三基因共过表达组细胞的SCP3信使RNA和蛋白质表达水平最高,这表明三基因共过表达具有将gBMSCs转分化为生殖细胞的最大潜力。综上所述,这些结果表明,STRA8、BOULE和DAZL的过表达能够在体外促进gBMSCs向早期山羊生殖细胞样细胞的转分化,这可能增强了减数分裂的成熟和进程。这种方法对于未来基础科学以及潜在临床应用中产生配子具有重要意义。