Early Ultrastructural Glomerular Alterations in Neonatal Nephrotic Mice (ICGN Strain)
Author(s) -
Atsuo Ogura,
H. Fujimura,
Takashi Asano,
M. Koura,
Ichiro Naito,
Yasushi Kobayashi
Publication year - 1995
Publication title -
veterinary pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.794
H-Index - 89
eISSN - 1544-2217
pISSN - 0300-9858
DOI - 10.1177/030098589503200317
Subject(s) - glomerular basement membrane , glomerulus , basement membrane , nephrotic syndrome , ultrastructure , glomerulonephritis , endocrinology , biology , medicine , pathology , microbiology and biotechnology , anatomy , kidney
ICGN is a strain of mice with hereditary nephrotic syndrome of an unknown cause. In this study, early glomerular alterations in newborn ICGN mice were observed with electron microscopy to gain a better insight into the onset of the disease. Development of the glomeruli was normal until fusion of epithelial and endothelial basement membranes in the developing capillary stage. From the maturing glomerulus stage onward, the fused glomerular basement membrane (GBM) increased in thickness by excessive accumulation of the basement membrane material secreted from the epithelial cells. This accumulation was followed by overall loss of epithelial foot processes in the glomeruli. These findings indicate that the disease in ICGN mice is caused by some defect(s) in the GBM maturation process, which may be crucial for the generation of the glomerular permselectivity.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom