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An Efficient Sieving Method to Isolate Intact Glomeruli from Adult Rat Kidney
Published on: November 1, 2018
Histopathological atlas of renal diseases. Membranoproliferative glomerulonephritis
Franco Ferrario1, Maria Pia Rastaldi
1Renal Immunopathology Center, S. Carlo Borromeo Hospital and Nuova Nefrologia Research Association, Milan, Italy.
Abstract:
Membranoproliferative glomerulonephritis (MPGN) is histologically characterized by intense glomerular hypercellularity (mainly due to mesangial proliferation) and diffuse thickening of the glomerular basement membrane with the appearance of ""double contours"". Two distinct histological forms have been identified--Type I MPGN and Type II MPGN. Type I MPGN is characterized by the predominant presence of subendothelial deposits, while Type II MPGN presents dense homogenous deposits in the basement membrane. Actually, despite many morphological and clinical similarities, there are enough histological and immunohistological differences to suggest that Type II MPGN is a separate and distinct entity, caused by different pathogenetic and morphogenetic mechanisms. Some researchers have identified a further entity: Type III MPGN, characterized by the concomitant presence of subendothelial and subepithelial deposits, but many authors at present believe that Type III MPGN is a morphological variant of Type I MPGN, given their clinical, immunological, and immunohistological similarities
Insights
Membranoproliferative glomerulonephritis (MPGN) presents distinct histological types. Type I MPGN shows subendothelial deposits, while Type II MPGN has dense deposits, suggesting different disease mechanisms.
Area of Science:
- Nephrology
- Pathology
- Immunology
Background:
- Membranoproliferative glomerulonephritis (MPGN) is a kidney disease characterized by specific histological features.
- Key features include glomerular hypercellularity, mesangial proliferation, and thickened glomerular basement membranes with "double contours".
Purpose of the Study:
- To differentiate the histological subtypes of MPGN.
- To explore the distinct pathogenetic and morphogenetic mechanisms underlying MPGN types.
- To clarify the classification of a potential Type III MPGN.
Main Methods:
- Histological examination of kidney biopsies.
- Immunohistological analysis of glomerular deposits.
- Morphological comparison of different MPGN types.
Main Results:
- Two primary histological forms of MPGN were identified: Type I and Type II.
- Type I MPGN is defined by subendothelial deposits.
- Type II MPGN is characterized by dense, homogeneous deposits within the basement membrane.
- Type III MPGN, with combined subendothelial and subepithelial deposits, is considered by many to be a variant of Type I MPGN due to similarities.
Conclusions:
- Histological and immunohistological differences support Type II MPGN as a distinct entity from Type I MPGN.
- Type II MPGN likely arises from different pathogenetic mechanisms compared to Type I.
- The classification of Type III MPGN remains debated, with a strong possibility of it being a variant of Type I MPGN.
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