CXCR4-expressing Mesenchymal Stem Cells Derived Nanovesicles for Rheumatoid Arthritis Treatment.
Jingjing GanXiaoxuan ZhangGuangcai ChenXubin HaoYuan Jin ZhaoLingyun SunPublished in: Advanced healthcare materials (2023)
Cell membrane camouflage technology, which has a demonstrated value for the bionic replication of natural cell membrane properties, is an active area of ongoing research readily applicable to nanomedicine. How to realize immune evasion, slow down the clearance from the body and improve targeting are still worth great efforts for this technology. Herein, we present novel cell membrane-mimicked nanovesicles from genetically engineered mesenchymal stem cells (MSCs) as a potential anti-inflammatory platform for rheumatoid arthritis (RA) management. Utilizing the synthetic biology approach, the biomimetic nanoparticles were constructed by fusing C-X-C motif chemokine receptor4 (CXCR4)-anchored MSC membranes onto drug-loaded polymeric cores (MCPNs), which make them ideal decoys of stromal cell-derived factor-1 (SDF-1)-targeted arthritis. These resulting nanocomplexes function to escape from the immune system, and enhance accumulation in the established inflamed joints via the CXCR4/SDF-1 chemotactic signal axis, thereby achieving an affinity to activated macrophages and synovial fibroblasts. It is further demonstrated that the MCPNs could significantly suppress synovial inflammation and relieve pathological conditions with favorable safety properties in collagen-induced arthritis mice. Our findings indicate the clinical values of MCPNs as biomimetic nanodrugs for RA therapy and related diseases. This article is protected by copyright. All rights reserved.
Keyphrases
- rheumatoid arthritis
- mesenchymal stem cells
- cancer therapy
- umbilical cord
- disease activity
- drug delivery
- bone marrow
- anti inflammatory
- cell migration
- ankylosing spondylitis
- cell therapy
- interstitial lung disease
- drug induced
- oxidative stress
- tissue engineering
- diabetic rats
- wastewater treatment
- high glucose
- wound healing
- stem cells
- extracellular matrix
- risk assessment
- drug release
- systemic lupus erythematosus
- skeletal muscle
- metabolic syndrome
- type diabetes
- insulin resistance
- mass spectrometry
- replacement therapy
- systemic sclerosis
- human health
- wild type
- adverse drug
- capillary electrophoresis