Detection of immunoreactive napsin A in human urine

被引:3
作者
Schauer-Vukasinovic, V
Langen, H
Giller, T
机构
[1] Axovan Ltd, Innovat Ctr, CH-4123 Allschwil, Switzerland
[2] Morphochem AG, D-81379 Munich, Germany
[3] F Hoffmann La Roche & Co Ltd, Div Pharma, Roche Genet, CH-4002 Basel, Switzerland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2000年 / 1524卷 / 01期
关键词
human napsin A; urine; human kidney; napsin antibody; aspartic proteinase;
D O I
10.1016/S0304-4165(00)00141-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human napsin A is an aspartic proteinase highly expressed in kidney and lung. To elucidate whether napsin A is excreted in the urine we have performed an immunochemical study using anti-napsin A polyclonal antibody. As a result an immunoreactive band at approx. 38 kDa was detected which corresponds to the molecular mass of recombinant active human napsin A. A deglycosylation study showed that excreted napsin A is N-glycosylated on apparently all of the three potential glycosylation sites. Immunoreactive napsin A was also observed in urine from patients with a transplanted kidney whose kidney function appeared half to fully normal. On the other hand, no or very low immunostaining was detected in samples from patients with diseased kidneys. The urinary excretion pattern correlates well with the enzymatic activity of napsin A. These data show that human napsin A is excreted as functional proteinase in the urine. Furthermore, immunochemical studies suggest a relation between urinary excretion of napsin A and renal function. More specifically, lack of urinary excretion of napsin A could potentially serve as a tool for the detection of kidney dysfunction. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:51 / 56
页数:6
相关论文
共 17 条
[1]  
BENIGNI A, 1995, LAB INVEST, V73, P461
[2]   Napsin A, a member of the aspartic protease family, is abundantly expressed in normal lung and kidney tissue and is expressed in lung adenocarcinomas [J].
Chuman, Y ;
Bergman, AC ;
Ueno, T ;
Saito, S ;
Sakaguchi, K ;
Alaiya, AA ;
Franzén, B ;
Bergman, T ;
Arnott, D ;
Auer, G ;
Appella, E ;
Jörnvall, H ;
Linder, S .
FEBS LETTERS, 1999, 462 (1-2) :129-134
[3]  
DAMICO G, 1991, AM J KIDNEY DIS, V17, P48
[4]  
EDDY AA, 1991, AM J PATHOL, V138, P1111
[5]  
Khan AR, 1998, PROTEIN SCI, V7, P815
[6]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[7]   TUBULOINTERSTITIAL LESIONS IN HUMAN MEMBRANOUS GLOMERULONEPHRITIS - RELATIONSHIP TO PROTEINURIA [J].
MAGIL, AB .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1995, 25 (03) :375-379
[8]   Molecular cloning of a novel mouse aspartic protease-like protein that is expressed abundantly in the kidney [J].
Mori, K ;
Ogawa, Y ;
Tamura, N ;
Ebihara, K ;
Aoki, T ;
Muro, S ;
Ozaki, S ;
Tanaka, I ;
Tashiro, K ;
Nakao, K .
FEBS LETTERS, 1997, 401 (2-3) :218-222
[9]  
PRESCOTT LF, 1966, CLIN SCI, V31, P425
[10]  
REMMUZI G, 1995, CURR OPIN NEPHROL HY, V4, P339