Hyaline glomerulopathy is a spontaneous disease of undetermined etiology that occurs sporadically in various strains of aging mice. In our laboratory, this disease was observed with unusual ultrastructural features as an incidental finding in 2 female B6C3FI mice from 2 carcinogenicity bioassays. Microscopically, renal lesions were characterized by marked diffuse enlargement and prominent hyalinization of the glomeruli, equally affecting both kidneys. Affected glomeruli were PAS positive, but were negative for amyloid by the Congo red method. Immunocytochemical staining revealed weakly positive glomerular deposits with polyclonal anti-mouse IgG-IgM-IgA cocktail. Ultrastructurally, there were characteristic subendothelial osmiophilic deposits composed of loosely-packed linear structures in the glomeruli. Lamellae, which appeared as fibrils in perpendicular sections, were relatively uniform, measured 6.1-17.01 nm in diameter, and formed single or double-layered structures. The ultrastructural and immunocytochemical characteristics are suggestive of a spontaneous immune-mediated mechanism in a strain of mouse commonly used in toxicology studies.Keywords. Hyaline glomerulopathy; ultrastructure; lamellae; kidney; mouse Hyaline glomerulopathy, also known as glomerulosclerosis (7,8,12,16,20) or glomerulonephritis (1 1 , 13,14,17), is a spontaneous disease of undetermined etiology that occurs sporadically in various strains of aging mice. The pathogenesis of this condition'is uncertain, but based on the ultrastructural and immunocytochemical characteristics, it is widely regarded as being of an immune origin. In our laboratory, an unusual presentation of this disease was observed as an incidental finding in 2 B6C3F1 females of 920 animals from 2 carcinogenicity bioassays. This report is intended to extend earlier observations on the incidence of spontaneous hyaline glomerulopathy in mice to include the B6C3F1 strain, which is commonly used in toxicology studies.The 2 affected mice were obtained from a commercial supplier (Charles River Canada, In& St Constant, Quebec), housed singly, and maintained within the guidelines of the Animals for Research Act of Ontario, 1971. Food (Purina Certified Rodent Chow #5002) and water were supplied ad li-
bittiin.At necropsy, kidneys were fixed in 10% neutral buffered formalin and processed routinely for light and ultraviolet microscopy. Paraffin-embedded sections of kidney were stained with hematoxylin and eosin (H&E), Periodic Acid-Schiff (PAS), or Congo red. H&E stained sections of formalin-fixed tissue were illuminated by incident liglit fluorescence and examined on a Zeiss Axiophot microscope (BP 450-490, FT 510, LP 520) (Zeiss, Canada). Formalinfixed pieces of kidney were also fixed overnight in universal fixative, washed in phosphate buffer, and post-fixed in 1% osmium tetroxide at room temperature. Kidney samples were then washed in phosphate buffer, dehydrated, cleared and embedded in Epon-Araldite. Thin sections were stained with uranyl acetate, followed by lead citr...