Angiotensinogen and AT(1) antisense inhibition of osteopontin translation in rat proximal tubular cells.
Journal
  American journal of physiology. Renal physiology.
Citation
  Am J Physiol Renal Physiol. 278(5):F708-16
Publication date
  2000 May
Authors
  Ricardo SD
Franzoni DF
Roesener CD
Crisman JM
Diamond JR
Investigators
  Jacqueline M. Crisman
Grant agencies
  National Institute of Child Health and Human Development
National Institute of Diabetes and Digestive and Kidney Diseases
Grants
  NICHD NO1-HD-73263
NIDDK RO1-DK-53163-01A1
MeSH headings
  Angiotensinogen
Kidney Tubules, Proximal
Receptors, Angiotensin
Sialoglycoproteins
MeSH qualifiers
  antagonists & inhibitors
metabolism
genetics
Abstract
  Antisense oligonucleotide inhibition of angiotensinogen and ANG II type 1 receptor (AT(1)) mRNA translation in rat proximal tubules (PT) was examined to provide direct evidence for a role of the renin-angiotensin system (RAS) in upregulated osteopontin expression observed following mechanical cell stretch. Male Sprague-Dawley rats underwent unilateral ureteral obstruction (UUO) under Brevital anesthesia. In situ hybridization and Western blot analysis demonstrated angiotensinogen mRNA and angiotensin converting enzyme (ACE) protein localized to PTs and upregulated in obstructed kidneys, respectively, confirming an increased expression of renal RAS in vivo. In vitro studies were performed to provide mechanistic insight into ANG II-dependent osteopontin expression following mechanical cell stretch, which putatively mimics the increased PT luminal pressure post-UUO. A cationic transfection method was used to introduce either angiotensinogen or AT(1) antisense oligonucleotide into cultured rat PT cells prior to 1 h of cyclic mechanical cell stretch. Northern blot analysis revealed that PT cells subjected to cyclic mechanical stretch with/without prior transfection with a sense oligonucleotide exhibited increased osteopontin mRNA expression compared with unstretched cells. Blockade of either angiotensinogen or AT(1) mRNA translation by antisense oligonucleotide inhibition prior to cell stretch was found to significantly decrease osteopontin mRNA levels 2.4-fold (P<0.004) and 1.6-fold (P<0.001), respectively, compared with values observed in control unstretched cells. This study provides evidence that stretch-induced upregulation of osteopontin mRNA expression is mediated, in part, via production of ANG II. These results lend insight into upregulation of osteopontin via a local PT RAS leading to macrophage infiltration in the tubulointerstitium in experimental hydronephrosis.
Medline ID
  20268248