Effectiveness of a novel rat model of off-target PLA2R1 knockout to renal impairment.

Abstract

Phospholipase A2 receptor 1 (PLA2R1) plays a crucial role in various diseases, including membranous nephropathy. However, the precise implications of PLA2R1 deficiency remain poorly understood. In this study, we created PLA2R1 knockout rats to explore potential consequences resulting from the loss of the PLA2R1 gene. Unexpectedly, our PLA2R1 knockout rats exhibited symptoms resembling those of chronic kidney disease after an 8-week observation period. Notably, several rats developed persistent proteinuria, a hallmark of renal dysfunction. Immunohistochemical and immunofluorescence analyses revealed insignificant glomerular fibrosis, reduced podocyte count, and augmented glomerular expression of complement C3 (C3) compared to immunoglobin A (IgA) and immunoglobin G(IgG) in the rat model. These findings suggest that the loss of PLA2R1 may contribute to the pathogenesis of membranous nephropathy and related conditions. Our knockout rat model provides a valuable tool for investigating the underlying pathology of PLA2R1-associated diseases, and may facilitate the development of targeted therapies for membranous nephropathy and other related disorders.

• Authors: Bo Huang, Zitong Zhang, Wendong Sui, Lu Zhao, Yinyin Li, Li Feng, Daihe Yang, Yun Zhou
• Journal: Genomics (Genomics) Vol. 116 Issue 2 Pg. 110796 (Mar 2024) ISSN: 1089-8646 [Electronic] United States
• PMID: 38237745 (Publication Type: Journal Article)
• Copyright: Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Chemical References

• Autoantibodies
• Receptors, Phospholipase A2

Topics

• Animals
• Rats
• Autoantibodies
• Glomerulonephritis, Membranous (genetics, diagnosis, metabolism)
• Receptors, Phospholipase A2 (genetics, metabolism)