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Expression and cellular localization of inducible nitric oxide synthase in lipopolysaccharide-treated rat kidneys.

Authors :
Choi JY
Nam SA
Jin DC
Kim J
Cha JH
Source :
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society [J Histochem Cytochem] 2012 Apr; Vol. 60 (4), pp. 301-15. Date of Electronic Publication: 2012 Jan 19.
Publication Year :
2012

Abstract

Although inducible nitric oxide synthase (iNOS) is known to play significant roles in the kidney, its renal localization has long been controversial. To resolve this issue, the authors identified iNOS-positive cell types in rat kidneys using double immunohistochemistry and confirmed iNOS positivity using enzyme histochemistry with NADPH-diaphorase (NADPH-d) and in situ RT-PCR. Adult male Sprague-Dawley rats were injected intraperitoneally with lipopolysaccharide (LPS) or saline as a control and sacrificed at various time intervals after injection. Quantitative real-time reverse transcriptase polymerase chain reaction showed that iNOS was not expressed in control kidneys but was induced in LPS-treated kidneys. iNOS immunostaining was strongest 6 to 18 hr after injection and decreased gradually to control levels by day 7. Double immunohistochemistry and NADPH-d revealed that iNOS expression was induced in the interstitial cells, glomerular parietal epithelial cells, the proximal part of the short-looped descending thin limb, the upper and middle papillary parts of the long-looped descending thin limb, some inner medullary collecting duct cells, and almost all calyceal and papillary epithelial cells. The present study determines the precise localization of iNOS in LPS-treated rat kidneys and provides an important morphological basis for examining the roles of iNOS in sepsis-induced acute kidney injury.

Details

Language :
English
ISSN :
1551-5044
Volume :
60
Issue :
4
Database :
MEDLINE
Journal :
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
Publication Type :
Academic Journal
Accession number :
22260992
Full Text :
https://doi.org/10.1369/0022155411436131