Song Renfang, Yosypiv Ihor V
Section of Pediatric Nephrology, Department of Pediatrics, Hypertension and Renal Center of Excellence, Tulane University Health Sciences Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA.
Int J Nephrol. 2011;2011:247048. doi: 10.4061/2011/247048. Epub 2011 Jun 20.
The renin-angiotensin system (RAS), a key regulator of the blood pressure and fluid/electrolyte homeostasis, also plays a critical role in kidney development. All the components of the RAS are expressed in the developing metanephros. Moreover, mutations in the genes encoding components of the RAS in mice or humans are associated with a broad spectrum of congenital anomalies of the kidney and urinary tract (CAKUT). These forms of CAKUT include renal papillary hypoplasia, hydronephrosis, duplicated collecting system, renal tubular dysgenesis, renal vascular abnormalities, and aberrant glomerulogenesis. Emerging evidence indicates that (pro)renin receptor (PRR), a novel component of the RAS, is essential for proper kidney development and that aberrant PRR signaling is causally linked to cardiovascular and renal disease. This paper describes the role of the RAS in kidney development and highlights emerging insights into the cellular and molecular mechanisms by which the PRR may regulate this critical morphogenetic process.
肾素-血管紧张素系统(RAS)是血压和体液/电解质稳态的关键调节因子,在肾脏发育中也起着至关重要的作用。RAS的所有成分都在发育中的后肾中表达。此外,小鼠或人类中编码RAS成分的基因突变与广泛的先天性肾脏和尿路异常(CAKUT)有关。这些形式的CAKUT包括肾乳头发育不全、肾积水、重复集合系统、肾小管发育不全、肾血管异常和肾小球发生异常。新出现的证据表明,(前)肾素受体(PRR)是RAS的一种新成分,对正常的肾脏发育至关重要,并且PRR信号异常与心血管和肾脏疾病存在因果关系。本文描述了RAS在肾脏发育中的作用,并强调了对PRR可能调节这一关键形态发生过程的细胞和分子机制的新见解。