ABSTRACT
Mammary tumors are by far the most common tumors in female dogs and effective treatment relies on prompt and accurate diagnostic procedures. Canine mammary tumors may originate from various cell types, such as luminal epithelial, myoepithelial and stromal cells. This study aimed to differentiate luminal epithelial and myoepithelial lineages, using specific markers including AE1/AE3, Vimentin, and p63. Such data can be useful for prognosis. Canine mammary tumors were collected by surgical resection and tissue samples were investigated using the avidin-biotin-immunoperoxidase method with used primary antibodies against AE1/AE3, vimentin, and p63. Luminal epithelial-origin tumors were found to be immunoreactive with AE1/AE3 and vimentin monoclonal antibody, while myoepithelial-origin tumors were positive for p63 and vimentin . In addition, canine mixed tumors showed reactivity with all three antibodies. In summary, AE1/AE3, p63 and vimentin can be used as specific immunohistochemical markers to distinguish lumino-epithelial and myoepithelial lineages of canine mammary tumors.
Subject(s)
Antiporters/metabolism , Dog Diseases/metabolism , Mammary Neoplasms, Animal/metabolism , Membrane Proteins/metabolism , Myoepithelioma/metabolism , Neoplasms, Glandular and Epithelial/metabolism , Vimentin/metabolism , Animals , Cell Lineage , Dog Diseases/pathology , Dogs , Female , Immunoenzyme Techniques , Mammary Neoplasms, Animal/pathology , Myoepithelioma/pathology , Myoepithelioma/veterinary , Neoplasms, Glandular and Epithelial/pathology , Neoplasms, Glandular and Epithelial/veterinaryABSTRACT
Antibodies to collagenous and noncollagenous components of glomerular basement membrane (GBM) have been detected by immunoblotting in some sera from patients with various kinds of glomerulonephritis. A half proportion of patients with rapidly progressive glomerulonephritis (RPGN), chronic focal glomerulonephritis (CFGN), idiopathic membranous glomerulonephritis (MGN). IgA nephropathy and lupus nephritis (LE-GN) had IgG antibodies to heterogenous components in acid insoluble fraction of pepsin digested GBM. This acid insoluble fraction represented a complex of collagen and noncollagenous proteins of GBM. Following digestion of acid insoluble fraction with bacterial collagenase, the triple helical collagenous components of GBM were destroyed and released most likely of noncollagenous proteins. Antibodies to this noncollagenous proteins were found in only some patients with chronic glomerulonephritis (17.6%) and lupus nephritis (21.4%). Upon reaction with human placenta derived type IV collagen, different frequencies of antibody response were found in patients of different groups. However, all these reactive sera showed a similar immunoblotting pattern. The relationship between antibody response to antigenic components from human GBM or human placenta and pathogenesis of renal disease is unclear. However, the occurrence of spontaneous autoantibody response to some exposed GBM self antigens may mediate further renal destruction resulting in chronic ongoing stage of the disease.
Subject(s)
Antibody Formation/immunology , Basement Membrane/immunology , Glomerulonephritis/blood , Kidney Glomerulus/immunology , Electrophoresis, Polyacrylamide Gel , Evaluation Studies as Topic , Glomerulonephritis/classification , Glomerulonephritis/immunology , Humans , ImmunoblottingABSTRACT
Renal disease associated with Opisthorchis viverrini infection was investigated in Syrian golden hamsters. On the fourth week after infection with 100 viable metacercariae; anti-tegumental membrane antibodies were detected in the sera by immunofluorescence antibody technic and by enzyme-linked immunosorbent assay. Six weeks after infection tegumental and anti-tegumental membrane immune-complex and amyloid fibrils were found in the glomeruli. Amyloid was characterized to be AA protein. Acute proliferative glomerulonephritis associated with the brightest immune-complex deposits developed in week 8 after infection. Intensity of immune-complexes in all glomeruli were reduce gradually thereafter and replaced by amyloid. Progressive obsolescence of the glomeruli, tubular atrophy, interstitial inflammation and fibrosis associated with massive proteinuria and deterioration of renal function appeared in week 10 after infection toward the end of the experiment in week 38 after infection.
Subject(s)
Amyloidosis/pathology , Glomerulonephritis, IGA/pathology , Kidney Diseases/pathology , Opisthorchiasis/complications , Amyloidosis/diagnosis , Amyloidosis/etiology , Animals , Cricetinae , Disease Models, Animal , Evaluation Studies as Topic , Fluorescent Antibody Technique , Glomerulonephritis, IGA/diagnosis , Glomerulonephritis, IGA/etiology , Kidney Diseases/diagnosis , Kidney Diseases/etiology , Mesocricetus , Microscopy, ElectronABSTRACT
The protein compositions of homogenized metacercaria and adult Opisthorchis viverrini were characterized by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). The two different stages of O. viverrini parasite contained several protein components with very similar mobilities on SDS-PAGE gel. The reaction in immunoblots of sera from patients with opisthorchiasis demonstrated antibodies against heterogeneous protein components of metacercariae and adult O. viverrini parasites. Only the components of metacercariae with molecular weights of 190-200 kD, 132 kD and 107 kD reacted specifically with opisthorchiasis sera. This characteristic reaction pattern was not observed in any control sera of normal subjects or those infected with other parasites. Identical reactions were however also recognized in the sera of experimental infected hamsters with metacercariae, but did not occur with adult worm as the antigen for the immunoblotting reaction. This may indicate that these metacercariae-associated protein components have potential diagnostic value for opisthorchiasis.
