Shanmugam S, Corvol P, Gasc J M
Laboratoire de Médecine Expérimentale, Institut National de la Santé et de la Recherche Médicale Unite 36-Collège de France, Paris.
Am J Physiol. 1994 Dec;267(6 Pt 1):E828-36. doi: 10.1152/ajpendo.1994.267.6.E828.
The two subtypes (AT1A and AT1B) of the type 1 (AT1) angiotensin II receptor mRNA were localized by in situ hybridization in rat fetal tissues from day 11 to 19 of gestation and in the young rat from day 0 to 10 postpartum, by use of 35S-labeled cRNA probes. Both subtype mRNAs were present in the kidney and in the adrenal gland. Organs such as liver, lung, heart, and undifferentiated mesenchymes expressed only AT1A mRNA. In contrast to the adult, only AT1A subtype was expressed during fetal and postnatal periods in the pituitary gland. Large blood vessels (e.g., aorta and cerebral arteries) expressed exclusively AT1A mRNA during fetal stages. The expression of each subtype appears to be differentially regulated, in a tissue- and age-specific way. This spatotemporal regulation of AT1A and AT1B expression suggests that angiotensin II could act as a differentiation factor during organogenesis in addition to its classical role as a regulator of the cardiovascular system.
利用35S标记的cRNA探针,通过原位杂交技术在妊娠第11天至19天的大鼠胎儿组织以及产后第0天至10天的幼鼠中,对1型(AT1)血管紧张素II受体mRNA的两种亚型(AT1A和AT1B)进行了定位。两种亚型的mRNA均存在于肾脏和肾上腺中。肝脏、肺、心脏和未分化间充质等器官仅表达AT1A mRNA。与成年期不同,垂体在胎儿期和出生后仅表达AT1A亚型。大血管(如主动脉和脑动脉)在胎儿期仅表达AT1A mRNA。每种亚型的表达似乎以组织和年龄特异性的方式受到不同的调节。AT1A和AT1B表达的这种时空调节表明,血管紧张素II除了作为心血管系统的调节因子发挥其经典作用外,还可能在器官发生过程中充当分化因子。