Literature DB >> 1691533

Significance of urinary complement components in various glomerular diseases.

K Sakakibara1, T Urano, Y Takada, A Takada.   

Abstract

The concentrations of two components of the complement system (C1q and C3) were measured in the urine and blood in 10 normal subjects and 134 patients with primary and secondary glomerulonephritis by using a highly sensitive enzyme immunoassay. The values of urinary excretion of C1q and C3 were well correlated to the ratios of fractional clearance of these complement proteins to that of neutral dextran of 55 A, which was used to minimize the influences of glomerular sieving because of their comparable molecular size to these complement components. The rate of renal tubular reabsorption of C1q and C3 were at least 89.2 and 93.4% of filtrated C1q and C3, respectively. Urinary C1q and C3 were excreted significantly in cases of membranoproliferative glomerulonephritis (MPGN), membranous glomerulonephritis, IgA nephropathy with both mesangial and capillary immune complex (IC) deposit and also in case of active lupus nephritis. On the other hand, the concentrations of these complement components were low in case of minimal lesion nephrotic syndrome, mild proliferative glomerulonephritis, inactive lupus nephritis and diabetic nephropathy without any immune staining. There was a significant correlation between the urinary excretion of C1q or C3 and intraglomerular IC deposition, especially IC deposition along the glomerular capillary wall. However, the degree of the excretion of these proteins was not correlated to the degree or permselectivity of proteinuria. The correlations between urinary C1q and C3 were observed in cases of IgA nephropathy with both mesangial and capillary deposit and MPGN, although we couldn't see the correlation in the other glomerular diseases. It is suggested that urinary excretion of such complement components represents the fixation of complement by deposited intraglomerular IC. The measurement of urinary concentration of these complement components provides a new clue to investigation or diagnosis of glomerular diseases.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 1691533     DOI: 10.1016/0049-3848(90)90080-v

Source DB:  PubMed          Journal:  Thromb Res        ISSN: 0049-3848            Impact factor:   3.944


  3 in total

1.  Cellular specificity of murine renal C3 expression in two models of inflammation.

Authors:  B H Ault; H R Colten
Journal:  Immunology       Date:  1994-04       Impact factor: 7.397

2.  Properdin has an ascendancy over factor H regulation in complement-mediated renal tubular damage.

Authors:  Seiji Nagamachi; Isao Ohsawa; Hiyori Suzuki; Nobuyuki Sato; Hiroyuki Inoshita; Atsuko Hisada; Daisuke Honda; Mamiko Shimamoto; Yoshio Shimizu; Satoshi Horikoshi; Yasuhiko Tomino
Journal:  BMC Nephrol       Date:  2014-05-22       Impact factor: 2.388

3.  Molecular Mapping of Urinary Complement Peptides in Kidney Diseases.

Authors:  Ralph Wendt; Justyna Siwy; Tianlin He; Agnieszka Latosinska; Thorsten Wiech; Peter F Zipfel; Aggeliki Tserga; Antonia Vlahou; Harald Rupprecht; Lorenzo Catanese; Harald Mischak; Joachim Beige
Journal:  Proteomes       Date:  2021-12-13
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.