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[高水平雄激素促进人胚胎干细胞向雄性原始生殖细胞分化]

[High-level androgen enhances the differentiation of hESCs into male primordial germ cells].

作者信息

Cao Meng, Liu Han-Wen, Ning Song, Liu Jia-Yin, Qin Lian-Ju, Cui Yu-Gui

机构信息

State Key Laboratory of Reproductive Medicine / Clinical Center of Reproductive Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.

出版信息

Zhonghua Nan Ke Xue. 2020 Jun;26(6):487-498.

Abstract

OBJECTIVE

To observe the effects of different concentrations of testosterone on the differentiation of human embryonic stem cells (hESCs) into early male germ cells and investigate the potential impact of high-level androgen exposure in early pregnancy in women with polycystic ovary syndrome (PCOS) on the fertility and primordial germ cell reserve of the male offspring in adulthood.

METHODS

We used 2 μmol/L retinoic acid to induce the differentiation of hESCs (46, XY) into male germ cells in vitro and meanwhile treated them with testosterone (T) at 0 mol/L, 3×10-7 mol/L, 5×10-7 mol/L, 15×10-7 mol/L, 45×10-7 mol/L, and 135×10-7 mol/L, respectively. We collected the cell samples at 0, 4, 7 and 14 days to determine the expressions of the specific genes and compare the differentiation process and efficiency of the male germ cells in different stages.

RESULTS

There was no difference in the morphology of the hESCs treated with different concentrations of testosterone in the same differentiation stage. The expression of the marker gene DAZL in the primordial germ cells peaked on the 4th day of differentiation, significantly higher in the 15×10-7, 45×10-7 and 135×10-7 mol/L groups than in the 3×10-7 mol/L group (P < 0.05), and that of the specific gene SCP3 in the early-meiosis germ cells began to increase on the same day, more significantly in the 45×10-7mol/L than in the 3×10-7 mol/L and 5×10-7 mol/L groups (P < 0.01), and peaked on the 7th day, dramatically higher in the 15×10-7, 45×10-7 and 135×10-7 mol/L groups than in the 3×10-7 mol/L group (P < 0.01). Immunofluorescence staining and flow cytometry showed a T concentration-dependent increase in the expression of DAZL at 4 days and those of SCP3 and VASA at 7 days. Moreover, the expression of the androgen receptor (AR) in the hESCs began to rise on the 4th day and kept going up till the 14th day, higher in the high-concentration than in the low-concentration T groups in the same stage of differentiation, though with no statistically significant difference (P > 0.05).

CONCLUSIONS

Exposure to high-level androgen during the differentiation of hESCs into early male germ cells can induce earlier expression of AR and earlier differentiation of hESCs into early male germ cells, which may result in insufficient reserve of male primary germ cells in the male offspring of PCOS women and affect their fertility after adulthood. hESCs can be used as an in vitro model to study the effects of intrauterine hyperandrogen on the reproductive development of male offspring in PCOS patients, which is also contributive to researches on the etiology of male infertility.

摘要

目的

观察不同浓度睾酮对人胚胎干细胞(hESCs)向早期雄性生殖细胞分化的影响,并探讨多囊卵巢综合征(PCOS)女性孕早期高水平雄激素暴露对成年雄性子代生育力及原始生殖细胞储备的潜在影响。

方法

采用2 μmol/L视黄酸体外诱导hESCs(46, XY)向雄性生殖细胞分化,同时分别用0 mol/L、3×10-7 mol/L、5×10-7 mol/L、15×10-7 mol/L、45×10-7 mol/L和135×10-7 mol/L的睾酮(T)处理。于0、4、7和14天收集细胞样本,检测特定基因表达,比较不同阶段雄性生殖细胞的分化过程及效率。

结果

同一分化阶段,不同浓度睾酮处理的hESCs形态无差异。原始生殖细胞中标记基因DAZL的表达在分化第4天达到峰值,15×10-7、45×10-7和135×10-7 mol/L组显著高于3×10-7 mol/L组(P < 0.05);减数分裂早期生殖细胞中特定基因SCP3的表达于同日开始升高,45×10-7mol/L组较3×10-7 mol/L和5×10-7 mol/L组更显著(P < 0.01),并于第7天达到峰值,15×10-7、45×10-7和135×10-7 mol/L组显著高于3×10-7 mol/L组(P < 0.01)。免疫荧光染色和流式细胞术显示,4天时DAZL表达呈T浓度依赖性增加,7天时SCP3和VASA表达呈T浓度依赖性增加。此外,hESCs中雄激素受体(AR)的表达于第4天开始升高,至第14天持续上升,同一分化阶段高浓度T组高于低浓度T组,但差异无统计学意义(P > 0.05)。

结论

hESCs向早期雄性生殖细胞分化过程中暴露于高水平雄激素可诱导AR早期表达及hESCs向早期雄性生殖细胞的早期分化,这可能导致PCOS女性雄性子代的雄性原始生殖细胞储备不足,并影响其成年后的生育力。hESCs可作为体外模型,用于研究子宫内高雄激素对PCOS患者雄性子代生殖发育的影响,也有助于男性不育病因学的研究。

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