Peer-reviewed veterinary case report
TGF-β₁-siRNA delivery with nanoparticles inhibits peritoneal fibrosis.
- Journal:
- Gene therapy
- Year:
- 2015
- Authors:
- Yoshizawa, H et al.
- Affiliation:
- Department of Internal Medicine · Japan
- Species:
- rodent
Abstract
Gene therapies may be promising for the treatment of peritoneal fibrosis (PF) in subjects undergoing peritoneal dialysis (PD). However, a method of delivery of treatment genes to the peritoneum is lacking. We attempted to develop an in vivo small interfering RNA (siRNA) delivery system with liposome-based nanoparticles (NPs) to the peritoneum to inhibit PF. Transforming growth factor (TGF)-β1-siRNAs encapsulated in NPs (TGF-β1-siRNAs-NPs) dissolved in PD fluid were injected into the peritoneum of mice with PF three times a week for 2 weeks. TGF-β1-siRNAs-NPs knocked down TGF-β1 expression significantly in the peritoneum and inhibited peritoneal thickening with fibrous changes. TGF-β1-siRNAs-NPs also inhibited the increase of expression of α-smooth muscle actin-positive myofibroblasts. These results suggest that the TGF-β1-siRNA delivery system with NPs described here could be an effective therapeutic option for PF in subjects undergoing PD.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/25567535/