Urokinase, urokinase receptor, and plasminogen activator inhibitor-1 expression on podocytes in immunoglobulin A glomerulonephritis

The purpose of this study was to investigate the expression of urokinase-type plasminogen activator (uPA), uPA receptor (uPAR), and plasminogen activator inhibitor (PAI)-1 on podocytes in immunoglobulin A (IgA) glomerulonephritis (GN). Renal biopsy specimens from 52 IgA GN patients were deparaffiniz...

Full description

Saved in:
Bibliographic Details
Published inThe Korean journal of internal medicine Vol. 29; no. 2; pp. 176 - 182
Main Authors Lee, Ji-Hye, Oh, Mee-Hye, Park, Jae-Seok, Gil, Hye-Wook, Yang, Jong-Oh, Lee, Eun-Young, Hong, Sae-Yong
Format Journal Article
LanguageEnglish
Published Korea (South) The Korean Association of Internal Medicine 01.03.2014
대한내과학회
Subjects
Online AccessGet full text
ISSN1226-3303
2005-6648
2005-6648
DOI10.3904/kjim.2014.29.2.176

Cover

More Information
Summary:The purpose of this study was to investigate the expression of urokinase-type plasminogen activator (uPA), uPA receptor (uPAR), and plasminogen activator inhibitor (PAI)-1 on podocytes in immunoglobulin A (IgA) glomerulonephritis (GN). Renal biopsy specimens from 52 IgA GN patients were deparaffinized and subjected to immunohistochemical staining for uPA, PAI-1, and uPAR. The biopsies were classified into three groups according to the expression of uPA and uPAR on podocytes: uPA, uPAR, and a negative group. The prevalences of the variables of the Oxford classification for IgA GN were compared among the groups. On podocytes, uPA was positive in 11 cases and uPAR was positive in 38 cases; by contrast, PAI-1 was negative in all cases. Expression of both uPA and uPAR on podocytes was less frequently accompanied by tubulointerstitial fibrosis. Our results suggest a possible protective effect of podocyte uPA/uPAR expression against interstitial fibrosis.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
G704-001640.2014.29.2.010
ISSN:1226-3303
2005-6648
2005-6648
DOI:10.3904/kjim.2014.29.2.176