Katsu Yoshinao, Takasu Eri, Iguchi Taisen
Center for Integrative Bioscience, Okazaki National Research Institutes, Okazaki 444-8585, Japan.
Mol Cell Endocrinol. 2002 Sep 30;195(1-2):99-107. doi: 10.1016/s0303-7207(02)00184-3.
Perinatal treatment of female mice with natural or synthetic estrogens including diethylstilbestrol (DES) results in estrogen-independent persistent proliferation and cornification of the vaginal epithelium. However, the molecular mechanisms of the estrogen-independent changes have not been elucidated. To analyze the mechanism of estrogen-independent cell proliferation and cornification of the vaginal epithelium, we used differential display and determined specific genes expressed in neonatally DES-treated vagina. A candidate clone that designated DDV5 was identical to the serine protease, neuropsin that is reportedly expressed in the mouse central nervous system. We then analyzed the expression pattern of DDV5/neuropsin using Northern blot analysis. We found: (1). DDV5/neuropsin mRNA is expressed in vaginae from neonatally DES-treated ovariectomized mice but not in vaginae from ovariectomized control mice, (2). its expression is not detected in uteri from neonatally DES-treated mice, (3). DDV5/neuropsin is expressed in vaginae from normal intact mice during estrus. Furthermore, we found that DDV5/neuropsin mRNA rapidly decreased in vaginae after ovariectomy. DDV5/neuropsin was detected in vaginae from ovariectomized mice 48 h after estrogen treatment. These results suggest that DDV5/neuropsin is expressed in estrogen-stimulated mouse vagina, and its gene expression is regulated by estrogen. Neonatal DES exposure affects transcriptional control of DDV5/neuropsin in the mouse vagina, which results in persistent expression of DDV5/neuropsin even after ovariectomy, thus, DDV5/neuropsin may play a role in estrogen-independent persistent proliferation and cornification of the vaginal epithelium. Using in situ hybridization method, we found DDV5/neuropsin mRNA localized in epithelial cells but not stromal cells in vaginae. This is the first report on the gene expression of a serine-protease neuropsin in the mouse vagina, and as a marker of the estrogen-independent persistent proliferation and cornification of the vaginal epithelium.
用天然或合成雌激素(包括己烯雌酚,DES)对雌性小鼠进行围产期治疗,会导致阴道上皮出现不依赖雌激素的持续性增殖和角质化。然而,这种不依赖雌激素的变化的分子机制尚未阐明。为了分析阴道上皮不依赖雌激素的细胞增殖和角质化机制,我们采用差异显示法并确定了新生期经DES处理的阴道中表达的特定基因。一个名为DDV5的候选克隆与丝氨酸蛋白酶神经蛋白酶相同,据报道该酶在小鼠中枢神经系统中表达。然后,我们使用Northern印迹分析法分析了DDV5/神经蛋白酶的表达模式。我们发现:(1). DDV5/神经蛋白酶mRNA在新生期经DES处理的去卵巢小鼠的阴道中表达,但在去卵巢对照小鼠的阴道中不表达;(2). 在新生期经DES处理的小鼠的子宫中未检测到其表达;(3). DDV5/神经蛋白酶在正常完整小鼠发情期的阴道中表达。此外,我们发现去卵巢后阴道中DDV5/神经蛋白酶mRNA迅速减少。雌激素处理48小时后,在去卵巢小鼠的阴道中检测到DDV5/神经蛋白酶。这些结果表明,DDV5/神经蛋白酶在雌激素刺激的小鼠阴道中表达,其基因表达受雌激素调节。新生期暴露于DES会影响小鼠阴道中DDV5/神经蛋白酶的转录控制,这导致即使在去卵巢后DDV5/神经蛋白酶仍持续表达,因此,DDV5/神经蛋白酶可能在阴道上皮不依赖雌激素的持续性增殖和角质化中起作用。使用原位杂交方法,我们发现DDV5/神经蛋白酶mRNA定位于阴道的上皮细胞而非基质细胞中。这是关于丝氨酸蛋白酶神经蛋白酶在小鼠阴道中的基因表达的首次报道,并且作为阴道上皮不依赖雌激素的持续性增殖和角质化的标志物。