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J Clin Invest. 1998 Oct 15;102(8):1489-97.

Angiotensin induces the urinary peristaltic machinery during the perinatal period.

Author information

1
Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee 37232, USA.

Abstract

The embryonic development of mammalian kidneys is completed during the perinatal period with a dramatic increase in urine production, as the burden of eliminating nitrogenous metabolic waste shifts from the placenta to the kidney. This urine is normally removed by peristaltic contraction of the renal pelvis, a smooth muscle structure unique to placental mammals. Mutant mice completely lacking angiotensin type 1 receptor genes do not develop a renal pelvis, resulting in the buildup of urine and progressive kidney damage. In mutants the ureteral smooth muscle layer is hypoplastic and lacks peristaltic movements. We show that angiotensin can induce the ureteral smooth muscles in organ cultures of wild-type, but not mutant, ureteral tissues and that, in wild-type mice, expression of both renal angiotensin and the receptor are transiently upregulated at the renal outlet at birth. These results reveal a new role for angiotensin in the unique cellular adaptations of the mammalian kidney to the physiological stresses of postnatal life.

PMID:
9788961
PMCID:
PMC508998
DOI:
10.1172/JCI4401
[Indexed for MEDLINE]
Free PMC Article

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