Restoration of CPT1A-mediated fatty acid oxidation in mesothelial cells protects against peritoneal fibrosis

Abstract

Background: Peritoneal dialysis (PD) is limited by gradual fibrotic remodeling in the peritoneum, a process involving profibrotic response of mesothelial cells. However, the role of fatty acid oxidation (FAO) and carnitine palmitoyltransferase 1A (CPT1A) in this process remains unexplored. Methods: FAO and CPT1A expression were characterized in mesothelial cells from patients on long-term PD and from a mouse model of PD using multiple experimental methods, including single-cell sequencing, seahorse assay, real-time quantitative PCR, Western blot, and immunofluorescence staining. Overexpression of CPT1A was achieved in a human mesothelial cell line and in primary mouse mesothelial cells. Finally, genetic and pharmacological manipulations of CPT1A were performed in a mouse model of PD. Results: Herein, FAO and CPT1A expression were reduced in mesothelial cells from patients on long-term PD, which negatively correlated with expression of fibrogenic markers in these cells. This was corroborated in PD mice, as well as in mouse and human mesothelial cells incubated with transforming growth factor (TGF) β1. CPT1A overexpression in mesothelial cells, which prevented TGFβ1-induced suppression of mitochondrial respiration, restored cellular ATP levels and downregulated the expression of fibrogenic markers. Furthermore, restoration of FAO by overexpressing CPT1A in PD mice reversed profibrotic phenotype in mesothelial cells and reduced fibrotic lesions in the peritoneum. Treatment with the CPT1A activator C75 induced similar therapeutic benefit in PD mice. In contrast, inhibition of FAO with a CPT1 inhibitor caused more severe fibrosis in PD mice. Conclusions: A defective FAO is responsible for the profibrotic response of mesothelial cells and thus the peritoneal fibrogenesis. This aberrant metabolic state could be improved by modulating CPT1A in mesothelial cells, suggesting FAO enhancement in mesothelial cells is a potential treatment of peritoneal fibrosis.

Intercellular communication in peritoneal dialysis

“…Blockade of hyperglycolysis with 2-deoxyglucose suppressed profibrotic cellular phenotype and peritoneal fibrosis in mice. Another study ( Su et al, 2023 ) which analyzed the above scRNA-seq data proposed that reduction of fatty acid oxidation in mesothelial cells characterizes patients on long-term PD. Cell trajectory analysis showed that COL1A1+ mesothelial cells expressed vimentin and FN1, supporting that mesothelial cells underwent transitions to fibroblasts.…”

“…In the study of pulmonary fibrosis, PM 2.5 induces EndMT by regulating the TGF-β1/Smad3 pathway ( Ma et al, 2020 ). TGF-β1 levels were increased in both peritoneal tissue and effluent of PD mice ( Su et al, 2023 ). It is possible that the TGF-β signaling pathway is involved in endothelial-mesenchymal transition in peritoneal fibrosis.…”