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The PP2A inhibitor LB-100 mitigates lupus nephritis by suppressing tertiary lymphoid structure formation.
- Source :
-
European journal of pharmacology [Eur J Pharmacol] 2024 Aug 15; Vol. 977, pp. 176703. Date of Electronic Publication: 2024 Jun 03. - Publication Year :
- 2024
-
Abstract
- Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by multi-organ involvement and autoantibody production. Patients with SLE face a substantial risk of developing lupus nephritis (LN), which imposes a substantial burden on both patients and their families. Protein phosphatase 2A (PP2A) is a widely distributed serine/threonine phosphatase that participates in regulating multiple signaling pathways. Inhibition of PP2A has been implicated in the treatment of various diseases. LB-100, a small molecule inhibitor of PP2A, has demonstrated anti-tumor therapeutic effects and high safety profile in preclinical experiments. However, the role of PP2A and its inhibitor has been insufficiently studied in LN. In this study, we assessed the potential effects of LB-100 in both MRL/lpr mice and R848-induced BALB/c mice. Our findings indicated that LB-100 administration led to reduced spleen enlargement, decreased deposition of immune complexes, ameliorated renal damage, and improved kidney function in both spontaneous and R848-induced lupus mouse models. Importantly, we observed the formation of tertiary lymphoid structures (TLSs) in the kidneys of two distinct lupus mouse models. The levels of signature genes of TLS were elevated in the kidneys of lupus mice, whereas LB-100 mitigated chemokine production and inhibited TLS formation. In addition, we confirmed that inhibition or knockdown of PP2A reduced the production of T cell-related chemokines by renal tubular epithelial cells (RTEC). In summary, our study highlighted the renal protective potential of the PP2A inhibitor LB-100 in two distinct lupus mouse models, suggesting its potential as a novel strategy for treating LN and other autoimmune diseases.<br />Competing Interests: Declaration of competing interest The authors state that they do not possess any recognized conflicting financial interests or personal ties that could have potentially impacted the findings provided in this research.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Mice
Female
Mice, Inbred MRL lpr
Kidney drug effects
Kidney pathology
Kidney metabolism
Disease Models, Animal
Spleen drug effects
Spleen pathology
Spleen immunology
Enzyme Inhibitors pharmacology
Enzyme Inhibitors therapeutic use
Piperazines
Protein Phosphatase 2 antagonists & inhibitors
Protein Phosphatase 2 metabolism
Lupus Nephritis drug therapy
Lupus Nephritis pathology
Tertiary Lymphoid Structures pathology
Mice, Inbred BALB C
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0712
- Volume :
- 977
- Database :
- MEDLINE
- Journal :
- European journal of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 38839028
- Full Text :
- https://doi.org/10.1016/j.ejphar.2024.176703