1. New Anti-Nephrin Antibody Mediated Podocyte Injury Model Using a C57BL/6 Mouse Strain
- Author
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Yasuo Takeuchi, Naoko Ishigaki, Nagako Kawashima, Kouju Kamata, Takashi Sano, Kazuhiro Takeuchi, and Shokichi Naito
- Subjects
0301 basic medicine ,Male ,Pathology ,medicine.medical_specialty ,Nephrotic Syndrome ,030232 urology & nephrology ,Strain (injury) ,urologic and male genital diseases ,Kidney ,Antibodies ,Podocyte ,Nephrin ,03 medical and health sciences ,Mice ,0302 clinical medicine ,Focal segmental glomerulosclerosis ,medicine ,Animals ,Humans ,biology ,urogenital system ,business.industry ,Glomerulosclerosis, Focal Segmental ,Podocytes ,Body Weight ,Glomerulosclerosis ,Membrane Proteins ,C57BL/6 Mouse ,medicine.disease ,female genital diseases and pregnancy complications ,Mice, Inbred C57BL ,Proteinuria ,Urodynamics ,030104 developmental biology ,medicine.anatomical_structure ,HEK293 Cells ,biology.protein ,Female ,Injury model ,Rabbits ,Antibody ,business - Abstract
Background: Focal segmental glomerulosclerosis (FSGS) is considered a subset of the podocytopathies. The molecular pathogenesis of podocytopathy is still unknown. There has not been an experimental animal model of isolated podocytopathy induced by antibody in C57BL/6 strain, which is widely used as the genetic background. Nephrin is closely associated with the slit diaphragm of the glomerular podocyte, and has recently received attention as a potential therapeutic target. The function of nephrin, especially its role in FSGS development via podocytopathy, is being elucidated. We report our experience with a C57BL/6 FSGS model induced by polyclonal rabbit anti-mouse nephrin antibody (α-mNep Ab). Methods: α-mNep Ab, which was generated by genetic immunization, was administered into C57BL/6 mice at once, intravenously. Urinary protein excretion, the development of glomerulosclerosis and the number of podocyte in mouse kidney were evaluated. Results: The α-mNep Ab-induced FSGS was associated with massive proteinuria and nephrotic syndrome. In periodic acid-Schiff staining, FSGS was observed from day 7 after antibody injection. Podocyte numbers and podocyte marker (anti-Wilms tumor 1 and anti-synaptopodin)-positive areas were clearly decreased. These results suggest that this FSGS mouse model reliably reproduces the human nephrotic syndrome and FSGS. Conclusion: We succeeded in making the nephrotic syndrome model mice induced by α-mNep Ab using C57BL/6. This model may be useful for studying the mechanisms of podocytopathy.
- Published
- 2017