Zehnder Daniel, Evans Katie N, Kilby Mark D, Bulmer Judith N, Innes Barbara A, Stewart Paul M, Hewison Martin
Division of Medical Sciences, The University of Birmingham, Queen Elizabeth Hospital, Birmingham, UK.
Am J Pathol. 2002 Jul;161(1):105-14. doi: 10.1016/s0002-9440(10)64162-4.
In addition to its classical calciotropic effects, the active form of vitamin D, 1,25-dihydroxyvitamin D(3) (1,25(OH)(2)D(3)) is a potent anti-proliferative/immunomodulatory secosteroid. The enzyme that catalyzes the synthesis of 1,25(OH)(2)D(3), 1alpha-hydroxylase (1alpha-OHase), is expressed in many human tissues, highlighting its possible role as an autocrine/paracrine activator of vitamin D. Immunohistochemical and RNA analyses were used to characterize the ontogeny of 1alpha-OHase expression in human placenta and decidua. Protein for 1alpha-OHase was detectable in trophoblast and decidua; the latter being stronger in decidualized stromal cells than macrophages, with no staining of lymphocytes. Quantitative reverse transcriptase-polymerase chain reaction was used to assess changes in mRNA expression for 1alpha-OHase at different gestations: first (mean, 9.1 +/- 1.5 weeks); second (mean, 14 +/- 1.8 weeks), and third trimester (mean, 39.3 +/- 2.5 weeks). 1alpha-OHase expression in decidua was approximately 1000-fold higher in first (95% confidence limits, 611 to 1376) and second (95% confidence limits, 633 to 1623) trimester biopsies when compared with the third trimester (95% confidence limits, 0.36 to 2.81) (both P < 0.001). In placenta, 1alpha-OHase expression was 80-fold higher in the first (range, 42 to 137) and second (range, 30 to 199) trimester when compared with third trimester biopsies (0.6 to 1.6) (both P < 0.001). Similar results were obtained by semiquantitative IHC. Parallel analysis of the receptor for 1,25(OH)(2)D(3) (vitamin D receptor) indicated that, as with 1alpha-OHase, highest levels of expression occurred in first trimester decidua. However, changes in vitamin D receptor mRNA expression across gestation were less pronounced than 1alpha-OHase. These spatiotemporal data emphasize the potential importance of 1alpha-OHase during early fetoplacental life and, in particular, suggest an autocrine/paracrine immunomodulatory function for the enzyme.
除了其经典的钙调节作用外,维生素D的活性形式,1,25 - 二羟基维生素D(3)(1,25(OH)₂D₃)是一种有效的抗增殖/免疫调节类固醇。催化1,25(OH)₂D₃合成的酶,1α - 羟化酶(1α - OHase),在许多人体组织中表达,突出了其作为维生素D自分泌/旁分泌激活剂的可能作用。免疫组织化学和RNA分析用于表征人胎盘和蜕膜中1α - OHase表达的个体发生。在滋养层和蜕膜中可检测到1α - OHase蛋白;后者在蜕膜化的基质细胞中比巨噬细胞更强,淋巴细胞无染色。定量逆转录 - 聚合酶链反应用于评估不同孕周时1α - OHase的mRNA表达变化:第一孕期(平均,9.1±1.5周);第二孕期(平均,14±1.8周)和第三孕期(平均,39.3±2.5周)。与第三孕期(95%置信限,0.36至2.81)相比,蜕膜中1α - OHase表达在第一孕期(95%置信限,611至1376)和第二孕期(95%置信限,633至1623)活检中约高1000倍(两者P<0.001)。在胎盘中,与第三孕期活检(0.6至1.6)相比,1α - OHase表达在第一孕期(范围,42至137)和第二孕期(范围,30至199)高80倍(两者P<0.001)。通过半定量免疫组织化学获得了类似结果。对1,25(OH)₂D₃受体(维生素D受体)的平行分析表明,与1α - OHase一样,最高表达水平出现在第一孕期蜕膜中。然而,整个孕期维生素D受体mRNA表达的变化不如1α - OHase明显。这些时空数据强调了1α - OHase在早期胎儿 - 胎盘生命期间的潜在重要性,特别是表明该酶具有自分泌/旁分泌免疫调节功能。