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Ontogeny of the mammalian kidney: expression of aquaporins 1, 2, 3, and 4
Lu Xing, Jian-Guo Wen, Jørgen Frøkiær, Jens Christian Djurhuus, Rikke Nørregaard
Aarhus, Denmark
Author Affiliations: Department of Clinical Medicine, Aarhus University, Denmark (Xing L, Frøkiær J, Djurhuus JC, Nørregaard R); Institute of Clinical Medicine, Pediatric Urodynamic Center, Urology, First Affiliated Hospital of Zhengzhou University, China (Wen JG)
Corresponding Author: Rikke Nørregaard, PhD, Department of Clinical Medicine, Aarhus University, Aarhus University Hospital, Skejby Brendstrupgårdsvej 100, DK-8200 Aarhus N, Denmark (Tel: 45-7845-9052; Email: rn@clin.au.dk)
doi: 10.1007/s12519-014-0508-7
Background: Determining the expression and functions of aquaporins (AQPs) in the adult kidney has generated important information about the roles of this protein family in the renal regulation of water homeostasis. However, limited information describes the expression of AQPs in fetal kidneys, and most reports on fetal renal AQPs originate from animal studies. Although there are the maturation and regulation of the renal-concentrating mechanism, the ways in which changes in the expression of AQPs contribute to the formation of urine during the perinatal period remain unclear.
Data sources: This review summarizes current knowledge about the spatial and temporal expression patterns of AQP1, AQP2, AQP3, and AQP4 in the fetal and postnatal kidneys in different animal species and in human beings.
Results: AQP1 and AQP2 expression can be detected earlier in gestation in human beings and sheep compared with mice and rats. AQP1 expression is detected earlier in the proximal tubules than the expression of AQP2, AQP3, and AQP4 in the collecting ducts.
Conclusion: Further studies investigating the regulation of AQPs during kidney development may provide insights into normal water-handling mechanisms and the pathophysiology of fetal kidneys, which may determine new directions for the clinical treatment of kidney diseases.
World J Pediatr 2014;10(4):306-312
Key words: aquaporin;
developing kidney;
fetal
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