Bebia Z, Somers J P, Liu G, Ihrig L, Shenker A, Zeleznik A J
Department of Cell Biology and Physiology, University of Pittsburgh School of Medicine, Pennsylvania 15261, USA.
Endocrinology. 2001 Jun;142(6):2252-9. doi: 10.1210/endo.142.6.8017.
This study was conducted to determine the feasibility of using replication-defective adenovirus vectors to express receptors for LH. Two vectors were constructed, one that directs the expression of wild-type human LH receptor (LHr; AdRSVLHrwt) and another that directs the expression of the constitutively activated D578H mutant human LH receptor (AdRSVD578HLHr). When infected with AdRSVwtLHr and AdRSVD578HLHr, COS-1 cells expressed LH/hCG-binding sites as reflected by specific binding of [(125)I]hCG. To determine the ability of the vectors to confer LH responsiveness, undifferentiated rat granulosa cells, which possess only FSH receptors, were infected with AdRSVwtLHr and AdRSVD578HLHR: Expression of the constitutively activated D578H LHr increased basal (gonadotropin-independent) estrogen and progesterone production. Expression of the wild-type LHr in granulosa cells did not stimulate basal steroid production, but conferred responsiveness to exogenous LH. For both wild-type LHr and D578HLHr, the absolute levels of steroid production were dependent upon the input of viral titers. Using these vectors, we compared effects of FSH and LH receptor activation in undifferentiated granulosa cells. Stimulation of undifferentiated granulosa cells by FSH and D578HLHr, as well as activation of wild-type LHr with LH resulted in comparable production of progesterone. In contrast, estradiol production in cells stimulated with FSH was greater than that in cells that expressed either D578H receptors or wild-type LHr in the presence of LH. Analysis of messenger RNAs (mRNAs) revealed that activations of FSH and the LH receptors were comparable in the induction of alpha-inhibin and 3betahydroxysteroid dehydrogenase mRNAS: However, activation of FSH receptor led to significantly greater expression of P450 aromatase and LHr mRNAs than did activation of LHR: These results suggest that activation of FSH and LH receptors in granulosa cells may differ with respect to activating intracellular signaling pathways and stimulating gene expression.
本研究旨在确定使用复制缺陷型腺病毒载体表达促黄体生成素(LH)受体的可行性。构建了两种载体,一种指导野生型人LH受体(LHr;AdRSVLHrwt)的表达,另一种指导组成型激活的D578H突变型人LH受体(AdRSVD578HLHr)的表达。当用AdRSVwtLHr和AdRSVD578HLHr感染时,COS-1细胞表达LH/hCG结合位点,这通过[(125)I]hCG的特异性结合得以体现。为了确定载体赋予LH反应性的能力,仅拥有促卵泡激素(FSH)受体的未分化大鼠颗粒细胞用AdRSVwtLHr和AdRSVD578HLHR进行感染:组成型激活的D578H LHr的表达增加了基础(不依赖促性腺激素)雌激素和孕酮的产生。颗粒细胞中野生型LHr的表达并未刺激基础类固醇的产生,但赋予了对外源LH的反应性。对于野生型LHr和D578HLHr,类固醇产生的绝对水平均取决于病毒滴度的输入。使用这些载体,我们比较了FSH和LH受体激活对未分化颗粒细胞的影响。FSH和D578HLHr对未分化颗粒细胞的刺激,以及用LH激活野生型LHr,导致孕酮的产生相当。相比之下,FSH刺激的细胞中雌二醇的产生大于在LH存在下表达D578H受体或野生型LHr的细胞中的雌二醇产生。信使核糖核酸(mRNA)分析显示,FSH和LH受体的激活在诱导α-抑制素和3β-羟基类固醇脱氢酶mRNA方面相当:然而,FSH受体的激活导致细胞色素P450芳香化酶和LHr mRNA的表达显著高于LHR的激活:这些结果表明,颗粒细胞中FSH和LH受体的激活在激活细胞内信号通路和刺激基因表达方面可能存在差异。