Chlorella-derived extracellular vesicle-based nanogels suppress cGAS-STING for treatment of radiation-induced lung injury.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41507189.
- Also identified by DOI 10.1038/s41467-025-68140-2 and PMC identifier 12881537.
- Licence recorded as CC BY-NC-ND.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Radiation-induced lung injury (RILI) represents a critical complication associated with radiation exposure, requiring targeted treatment strategies in clinical practice. Here, we pioneered the extraction of extracellular vesicles (EVs) from Chlorella and innovatively developed a multifunctional nanogel platform (RU.521-EVs NPs) by combining them with the cGAS inhibitor RU.521. The Chlorella-derived EVs possess a naturally high abundance of antioxidant enzymes (e.g., SOD2, CAT) and anti-inflammatory lipids (e.g., linolenic acid). RU.521-EVs NPs could synergistically inhibit excessive activation of the cGAS-STING pathway, and significantly reduce the secretion of pro-inflammatory factors. In the RILI mouse model, the nanogel demonstrated significant anti-inflammatory and anti-fibrosis activity, with no observed systemic toxicity. Their biological safety, cost-effectiveness, and multifaceted anti-radiation mechanisms of nanogels make them particularly beneficial in contexts such as medical radiation exposure, providing a strategy for the clinical translation of RILI that emphasizes both safety and long-term efficacy.
Medical subject headings
- Extracellular Vesicles
- Nucleotidyltransferases
- Nanogels
- Chlorella
- Membrane Proteins
- Lung Injury