CpG and Rutin Co-Loaded DNA Tetrahedra for Targeted Therapy of Intracerebral Hemorrhage: Synergistic Hematoma Clearance and Neuroinflammation Inhibition

被引:0
作者
Wang, Jing [1 ,2 ,3 ,4 ]
Xie, Nuli [2 ]
Lu, Shan [2 ]
Xiao, Bo [1 ,3 ,4 ]
Ou, Yangqin [2 ]
Li, Qingnian [2 ]
Liu, Dexian [2 ]
Zhou, Wenhu [2 ,5 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Sch Pharmaceut Sci, Changsha 410013, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Dept Neurol, Jiangxi Branch, Nanchang 330000, Jiangxi, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha 410008, Hunan, Peoples R China
[5] Key Lab Biol Nanotechnol Natl Hlth Commiss, Changsha 410008, Hunan, Peoples R China
基金
中国博士后科学基金;
关键词
DNA nanostructure; macrophage/microglia; oxidative stress; phagocytosis; targeting delivery; MACROPHAGES; EVACUATION; MICROGLIA; RECOVERY; INJURY;
D O I
10.1002/adfm.202403469
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Intracerebral hemorrhage (ICH) presents a formidable challenge due to its high mortality and disability rates, primarily attributed to cerebral hematoma formation and ensuing neuroinflammation. Swift hematoma removal is paramount for prognosis, yet existing interventions carry risks and limitations. Notably, elevated CD47 expression on hematoma-associated RBC triggers a "don't eat me" signal, impeding hematoma clearance, while microglial/macrophage erythrophagocytosis exacerbates oxidative stress and the RBC lysate evokes neuroinflammation. To address this conundrum, a multifunctional nanomedicine (TD-CFR), employing DNA tetrahedra (TD) as a carrier for ICH treatment is introduced. The investigations reveal that CpG enhances the phagocytosis of CD47-expressing RBC by microglia/macrophages via lipid metabolism modulation. Integration of CpG into TD preserves its pro-phagocytic efficacy, while TD's double-stranded region enables efficient encapsulation of Rutin, a potent anti-inflammatory and antioxidant flavonoid. Capitalizing on disrupted blood-brain barrier integrity at the hemorrhage site, TD-CFR achieves robust enrichment within cerebral hematoma post-intravenous administration, augmented by folate receptor-mediated targeting of microglia/macrophages. Efficacy assessments in mouse and rabbit ICH models confirm TD-CFR's therapeutic benefits, including hematoma clearance, neuroinflammation suppression, and brain function restoration. Leveraging TD's high biosafety profile and dual active ingredient loading capacity, the study unveils a promising drug treatment paradigm for ICH. CpG is found to circumvent CD47-mediated "don't eat me" signals and augment microglial/macrophage phagocytosis of RBC at the hemorrhage site, but increase oxidative stress post-phagocytosis. To this end, a multifunctional nanoparticle is developed to co-encapsulate CpG and Rutin within DNA tetrahedral carriers for targeting delivery, and these two active molecules function synergistically to restore immune cell phagocytosis and mitigate neuroinflammation. image
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页数:19
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