Rapamycin and Hyperoside-Co-loaded Macrophage Delivery System Enhanced Pulmonary Fibrosis Therapy by Autophagy Upregulation and Epithelial-to-Mesenchymal Transition Inhibition.
Qi WangYuanmeng NingJinru ZhangXu DuZihan XuYongcheng HuFeng GaoYanzuo ChenPublished in: ACS applied materials & interfaces (2024)
Pulmonary fibrosis is a lethal interstitial lung disease, for which current treatments are inadequate in halting its progression. A significant factor contributing to the development of fibrosis is insufficient autophagy, which leads to increased fibroblast proliferation and collagen deposition. However, treatments aimed at upregulating autophagy often cause further lung pathology due to the disruption of epithelial cell balance. In response, we have developed a novel macrophage delivery system loaded with an epithelial-to-mesenchymal transition inhibitor, hyperoside (HYP), and an autophagy inducer, rapamycin (RAP). This system targets the fibrotic areas of the lung through chemotaxis, releases liposomes via macrophage extracellular traps, and effectively inhibits fibroblast proliferation while restoring the alveolar structure through the combined effects of RAP and HYP, ultimately reducing lung pathology without causing systemic toxicity. Our findings not only highlight a promising method to enhance autophagy-based treatments for pulmonary fibrosis but also demonstrate the potential of macrophages as effective nanocarriers for drug delivery.
Keyphrases
- pulmonary fibrosis
- drug delivery
- signaling pathway
- cell death
- endoplasmic reticulum stress
- oxidative stress
- interstitial lung disease
- systemic sclerosis
- cancer therapy
- adipose tissue
- wound healing
- idiopathic pulmonary fibrosis
- rheumatoid arthritis
- poor prognosis
- mesenchymal stem cells
- replacement therapy
- drug induced
- smoking cessation