Casey M L, MacDonald P C, Andersson S
Cecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas 75235-9051.
J Clin Invest. 1994 Nov;94(5):2135-41. doi: 10.1172/JCI117569.
The cDNAs for two separate human 17 beta-hydroxysteroid dehydrogenases (17 beta-HSD) have been isolated and sequenced. The well-studied human placental cytosolic 17 beta-HSD (also referred to as estradiol dehydrogenase) preferentially catalyzes the reduction of estrone to estradiol-17 beta and the reduction of the C-20-ketone of progesterone to 20 alpha-dihydroprogesterone. This isoform of the enzyme has been referred to as 17 beta-HSD type 1 and localized to chromosome 17. A second 17 beta-HSD isoform (referred to as type 2) is localized in the endoplasmic reticulum of human trophoblast and is characterized by the preferential oxidation of the C-17 beta-hydroxyl group of C18- and C19-steroids and the C-20 alpha-hydroxyl group of 20 alpha-dihydroprogesterone. In this study, we determined the chromosomal localization of human 17 beta-HSD type 2, the expression of this gene in human endometrium, and the tissue distribution of the mRNA. We found that the human 17 beta-HSD type 2 gene is localized on chromosome 16, 16q24. 17 beta-HSD type 2 mRNA (approximately 1.5 kb) was identified in human endometrial tissues by Northern analysis of total RNA (10 micrograms). The highest levels of 17 beta-HSD type 2 mRNA were found in endometrial tissues obtained during the mid- to late secretory phase of the ovarian cycle (i.e., during the time of high plasma levels of progesterone). 17 beta-HSD type 2 mRNA levels were much greater in glandular epithelium than in the stromal cells isolated from secretory phase endometrium. The levels of 17 beta-HSD type 2 mRNA in secretory phase endometrium were approximately one-tenth that in villous trophoblast tissue from human placenta. We did not detect 17 beta-HSD type 1 mRNA in endometrial tissue by Northern analysis of total (10 micrograms) RNA. These findings are consistent with the view that the progestin-regulated 17 beta-HSD of the glandular epithelium of the human endometrium is primarily, if not exclusively, the product of the 17 beta-HSD type 2 gene. 17 beta-HSD type 2 mRNA was present in human placenta, liver, and small intestine; much smaller amounts, barely detectable by Northern analysis of poly(A)+ RNA, were present in prostate, kidney, pancreas, and colon, but not in heart, brain, skeletal muscle, spleen, thymus, ovary, or testis.
已分离并测序了两种不同的人17β-羟基类固醇脱氢酶(17β-HSD)的cDNA。经过充分研究的人胎盘胞质17β-HSD(也称为雌二醇脱氢酶)优先催化雌酮还原为雌二醇-17β以及孕酮的C-20-酮还原为20α-二氢孕酮。这种酶的同工型被称为17β-HSD 1型,定位于17号染色体。第二种17β-HSD同工型(称为2型)定位于人滋养层细胞的内质网,其特征是优先氧化C18和C19类固醇的C-17β-羟基以及20α-二氢孕酮的C-20α-羟基。在本研究中,我们确定了人17β-HSD 2型的染色体定位、该基因在人子宫内膜中的表达以及mRNA的组织分布。我们发现人17β-HSD 2型基因定位于16号染色体16q24。通过对总RNA(10微克)进行Northern分析,在人子宫内膜组织中鉴定出了17β-HSD 2型mRNA(约1.5 kb)。在卵巢周期的分泌中期至晚期获得的子宫内膜组织中发现17β-HSD 2型mRNA水平最高(即,在血浆孕酮水平较高时)。从分泌期子宫内膜分离出的腺上皮细胞中17β-HSD 2型mRNA水平比基质细胞中的高得多。分泌期子宫内膜中17β-HSD 2型mRNA水平约为人胎盘绒毛滋养层组织中的十分之一。通过对总RNA(10微克)进行Northern分析,我们在子宫内膜组织中未检测到17β-HSD 1型mRNA。这些发现与以下观点一致,即人子宫内膜腺上皮中受孕激素调节的17β-HSD主要(如果不是唯一)是17β-HSD 2型基因的产物。17β-HSD 2型mRNA存在于人胎盘、肝脏和小肠中;在前列腺、肾脏、胰腺和结肠中存在少量,通过对poly(A)+ RNA进行Northern分析几乎检测不到,但在心脏、大脑、骨骼肌、脾脏、胸腺、卵巢或睾丸中不存在。