Niimura F, Okubo S, Fogo A, Ichikawa I
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
Am J Physiol. 1997 Jan;272(1 Pt 2):R142-7. doi: 10.1152/ajpregu.1997.272.1.R142.
In situ hybridization for mouse angiotensinogen (Ao) mRNA was performed using a Stu I-Pst I 0.43-kb fragment of exon 2 as a template to synthesize RNA probes. The mouse Ao mRNA expression patterns were different from those reported for rats. Ao mRNA was expressed in the fetal liver as early as 12.5 days postcoitus, and the liver remained the predominant organ of its expression in utero. Within the developing kidney, Ao mRNA was demonstrated at 17.5 days postcoitus in the proximal straight tubules undergoing loop formation in the medulla. In the matured mouse kidney, the expression site is within the outer stripe of outer medulla, hence identified as the pars recta, not proximal convoluted tubules. Additional studies revealed that, in rats also, Ao mRNA was localized in the pars recta. This was in contrast to previously published results that showed that Ao mRNA was localized primarily in the proximal convoluted tubules in rats. Thus the pars recta appears to be an important intrarenal source of Ao for both rats and mice throughout pre- and postnatal periods, whereas the liver can be the major extrarenal source in utero in mice, but not in rats.
使用外显子2的0.43kb Stu I - Pst I片段作为模板合成RNA探针,进行小鼠血管紧张素原(Ao)mRNA的原位杂交。小鼠Ao mRNA的表达模式与大鼠的报道不同。Ao mRNA早在交配后12.5天就在胎儿肝脏中表达,并且肝脏在子宫内仍然是其表达的主要器官。在发育中的肾脏中,在交配后17.5天,在髓质中正在形成袢的近端直管中显示出Ao mRNA。在成熟的小鼠肾脏中,表达位点在外髓质的外带内,因此被确定为直部,而不是近端曲管。进一步的研究表明,在大鼠中,Ao mRNA也定位于直部。这与先前发表的结果相反,先前的结果表明Ao mRNA主要定位于大鼠的近端曲管中。因此,直部似乎是大鼠和小鼠在整个产前和产后时期肾内Ao的重要来源,而肝脏在小鼠子宫内可以是主要的肾外来源,但在大鼠中不是。