Duan Shouxing, Jiang Xuewu, Zhang Xuan, Xie Lei, Sun Zongbo, Ma Shuhua, Li Jianhong
Department of Radiology, The First Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China (mainland).
Department of Pediatric Surgery, The Second Affiliated Hospital of Shantou University Medical College, Shantou, Guangdong, China (mainland).
Med Sci Monit. 2016 Feb 8;22:416-21. doi: 10.12659/msm.895089.
BACKGROUND Hormonal effects on the gubernaculum can affect testicular descent. Diethylstilbestrol (DES) is a nonsteroidal synthetic estrogen that disrupts the outgrowth of gubernaculums, leading to testis maldescent. However, the underlying mechanisms remain elusive. MATERIAL AND METHODS The gubernaculum were removed from 3-day-old mice and cultured. The subcultured cells were randomly divided into a normal control group and experimental groups. The DES groups were administered 10 μg/ml, 1 μg/ml, 0.1 μg/ml, 0.01 μg/ml of diethylstilbestrol dissolved in dimethyl sulfoxide (DMSO) respectively. The cell morphology was observed under an inverted microscope, and leucine-rich repeat-containing G protein-coupled receptor 8 (LGR8) was localized by immunofluorescence. The expressions of LGR8 gene and protein in gubernaculum cells were quantified by RT-PCR and Flow Cytometer respectively. RESULTS DES treatment converted cells from a normal fibroblast-like morphology into a more refractile, spindle-shaped morphology or irregular elliptical shapes along with cytoplasmic shrinkage. LGR8 was expressed in the cytoplasmic membrane, DES dose-dependently downregulated LGR8 expression at low doses (≤1.0 μg/ml), but upregulated LGR8 at high doses (10 μg/ml) at both the mRNA and protein levels. CONCLUSIONS These results suggest that DES causes testicular maldescent by altering the LGR8 pathway in mouse gubernaculum testis cells.
背景 激素对睾丸引带的影响可影响睾丸下降。己烯雌酚(DES)是一种非甾体类合成雌激素,可破坏睾丸引带的生长,导致睾丸下降异常。然而,其潜在机制仍不清楚。
材料与方法 从3日龄小鼠中取出睾丸引带并进行培养。将传代培养的细胞随机分为正常对照组和实验组。DES组分别给予溶解于二甲基亚砜(DMSO)中的10μg/ml、1μg/ml、0.1μg/ml、0.01μg/ml己烯雌酚。在倒置显微镜下观察细胞形态,并用免疫荧光法对富含亮氨酸重复序列的G蛋白偶联受体8(LGR8)进行定位。分别用RT-PCR和流式细胞仪定量检测睾丸引带细胞中LGR8基因和蛋白的表达。
结果 DES处理使细胞从正常的成纤维细胞样形态转变为更具折光性的纺锤形形态或不规则椭圆形形态,同时伴有细胞质收缩。LGR8表达于细胞膜,低剂量(≤1.0μg/ml)时DES剂量依赖性下调LGR8表达,但高剂量(10μg/ml)时在mRNA和蛋白水平均上调LGR8表达。
结论 这些结果表明,DES通过改变小鼠睾丸引带细胞中的LGR8途径导致睾丸下降异常。