TY - JOUR
T1 - Nebulization of extracellular vesicles
T2 - A promising small RNA delivery approach for lung diseases
AU - Han, Yohan
AU - Zhu, Yin
AU - Youngblood, Hannah A.
AU - Almuntashiri, Sultan
AU - Jones, Timothy W.
AU - Wang, Xiaoyun
AU - Liu, Yutao
AU - Somanath, Payaningal R.
AU - Zhang, Duo
N1 - Funding Information:
This work was supported by National Institutes of Health (NIH) grants NIH/National Heart, Lung, and Blood Institute (NHLBI) R00 HL141685 and NIH/National Institute of Allergy and Infectious Diseases (NIAID) R03 AI152003 to D.Z. NIH/NIAID R03 AI169063 to X.W.
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/12
Y1 - 2022/12
N2 - Small extracellular vesicles (sEVs) are a group of cell-secreted nanovesicles with a diameter up to 200 nm. A growing number of studies have indicated that sEVs can reflect the pathogenesis of human diseases and mediate intercellular communications. Recently, sEV research has drastically increased due to their drug delivery property. However, a comprehensive method of delivering exogenous small RNAs-loaded sEVs through nebulization has not been reported. The methodology is complicated by uncertainty regarding the integrity of sEVs after nebulization, the delivery efficiency of aerosolized sEVs, their deposition in the lungs/cells, etc. This study demonstrates that sEVs can be delivered to murine lungs through a vibrating mesh nebulizer (VMN). In vivo sEV tracking indicated that inhaled sEVs were distributed exclusively in the lung and localized primarily in lung macrophages and airway epithelial cells. Additionally, sEVs loaded with small RNAs were successfully delivered into the lungs. The administration of siMyd88-loaded sEVs through inhalation reduced lipopolysaccharide (LPS)-induced lung injury in mice, supporting an application of this nebulization methodology to deliver functional small RNAs. Collectively, our study proposes a novel method of sEVs-mediated small RNA delivery into the murine lung through nebulization and presents a potential sEV-based therapeutic strategy for human lung diseases.
AB - Small extracellular vesicles (sEVs) are a group of cell-secreted nanovesicles with a diameter up to 200 nm. A growing number of studies have indicated that sEVs can reflect the pathogenesis of human diseases and mediate intercellular communications. Recently, sEV research has drastically increased due to their drug delivery property. However, a comprehensive method of delivering exogenous small RNAs-loaded sEVs through nebulization has not been reported. The methodology is complicated by uncertainty regarding the integrity of sEVs after nebulization, the delivery efficiency of aerosolized sEVs, their deposition in the lungs/cells, etc. This study demonstrates that sEVs can be delivered to murine lungs through a vibrating mesh nebulizer (VMN). In vivo sEV tracking indicated that inhaled sEVs were distributed exclusively in the lung and localized primarily in lung macrophages and airway epithelial cells. Additionally, sEVs loaded with small RNAs were successfully delivered into the lungs. The administration of siMyd88-loaded sEVs through inhalation reduced lipopolysaccharide (LPS)-induced lung injury in mice, supporting an application of this nebulization methodology to deliver functional small RNAs. Collectively, our study proposes a novel method of sEVs-mediated small RNA delivery into the murine lung through nebulization and presents a potential sEV-based therapeutic strategy for human lung diseases.
KW - Acute lung injury
KW - Exosome
KW - Inflammation
KW - Nebulizer
KW - miRNA
KW - siRNA
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U2 - 10.1016/j.jconrel.2022.10.052
DO - 10.1016/j.jconrel.2022.10.052
M3 - Article
C2 - 36341934
AN - SCOPUS:85141241217
SN - 0168-3659
VL - 352
SP - 556
EP - 569
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -