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绵羊水通道蛋白1:cDNA克隆、个体发生及肾脏基因表达的调控

Ovine AQP1: cDNA cloning, ontogeny, and control of renal gene expression.

作者信息

Wintour E M, Earnest L, Alcorn D, Butkus A, Shandley L, Jeyaseelan K

机构信息

Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Pediatr Nephrol. 1998 Sep;12(7):545-53. doi: 10.1007/s004670050502.

Abstract

The cDNA for the ovine aquaporin 1 (AQP1) was obtained and found to be 97%, 88%, and 85%, respectively, homologous to the bovine, human, and rat AQP1 cDNA. The level of total kidney mRNA expressed as a ratio to glyceraldehyde-3-phosphate dehydrogenase increased sevenfold from 60 days to 140 days of gestation (term=150 days) and reached adult values by 6 weeks after birth. Treatment of pregnant ewes (and their fetuses) at 64 and 74 days of gestation with dexamethasone (0.76 mg/h for 48 h) resulted in a small but statistically significant increase in AQP1 mRNA only in the 74-day fetuses. By immunohistochemistry, it was shown that the increase in AQP1 mRNA with dexamethasone resulted largely from an increase in maturity of the inner zone of the fetal renal cortex (i.e., more tubules) as well as stronger expression of AQP1 in proximal tubules and thin descending limbs of loops of Henle. A similar effect occurred in fetuses infused for 3 days with angiotensin I (6.7 microg/h) in the last third of gestation.

摘要

获得了绵羊水通道蛋白1(AQP1)的cDNA,发现其与牛、人和大鼠的AQP1 cDNA的同源性分别为97%、88%和85%。以甘油醛-3-磷酸脱氢酶为参照的总肾mRNA水平在妊娠60天至140天(足月为150天)期间增加了7倍,并在出生后6周达到成年水平。在妊娠64天和74天用皮质醇(0.76毫克/小时,持续48小时)处理怀孕母羊(及其胎儿),仅在74天的胎儿中导致AQP1 mRNA有小幅度但具有统计学意义的增加。通过免疫组织化学显示,皮质醇处理导致的AQP1 mRNA增加主要源于胎儿肾皮质内区(即更多肾小管)成熟度的增加以及近端小管和髓袢细降支中AQP1表达增强。在妊娠最后三分之一阶段给胎儿连续3天输注血管紧张素I(6.7微克/小时)也出现了类似效果。

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