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Polybutylcyanoacrylate nanoparticles for delivering hormone response element-conjugated neurotrophin-3 to the brain of intracerebral hemorrhagic rats
被引:27
作者:
Chung, Chiu-Yen
[1
]
Yang, Jen-Tsung
[2
,3
]
Kuo, Yung-Chih
[1
]
机构:
[1] Natl Chung Cheng Univ, Dept Chem Engn, Chiayi 62102, Taiwan
[2] Chang Gung Mem Hosp, Dept Neurosurg, Chiayi 61363, Taiwan
[3] Chang Gung Univ, Coll Med, Tao Yuan 33302, Taiwan
关键词:
Polybutylcyanoacrylate nanoparticle;
Neurotropnin-3;
Hormone response element;
Intracerebral hemorrhage;
Blood-brain barrier;
PLURIPOTENT STEM-CELLS;
NEURONAL DIFFERENTIATION;
MESSENGER-RNA;
IN-VITRO;
EXPRESSION;
APOPTOSIS;
HYPOXIA;
GROWTH;
DEXAMETHASONE;
SCAFFOLDS;
D O I:
10.1016/j.biomaterials.2013.08.083
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
Hypertensive intracerebral hemorrhage (ICH) is a rapidly evolutional pathology, inducing necrotic cell death followed by apoptosis, and alters gene expression levels in surrounding tissue of an injured brain. For ICH therapy by controlled gene release, the development of intravenously administrable delivery vectors to promote the penetration across the blood-brain barrier (BBB) is a critical challenge. To enhance transfer efficiency of genetic materials under hypoxic conditions, polybutylcyanoacrylate (PBCA) nanoparticles (NPs) were used to mediate the intracellular transport of plasmid neurotrophin-3 (NT-3) containing hormone response element (HRE) with a cytomegalovirus (cmv) promoter and to differentiate induced pluripotent stem cells (iPSCs). The differentiation ability of iPSCs to neurons was justified by various immunological stains for protein fluorescence. The effect of PBCA NP/cmvNT-3-HRE complexes on treating ICH rats was studied by immunostaining, western blotting and Nissl staining. We found that the treatments with PBCA NP/cmvNT-3-HRE complexes increased the capability of differentiating iPSCs to express NT-3, TrkC and MAP-2. Moreover, PBCA NPs could protect cmvNT-3-HRE against degradation with EcoRI/PstI and DNase I in vitro and raise the delivery across the BBB in vivo. The administration of PBCA NP/cmvNT-3-HRE complexes increased the expression of NT-3, inhibited the expression of apoptosis-inducing factor, cleaved caspase-3 and DNA fragmentation, and reduced the cell death rate after ICH in vivo. PBCA NPs are demonstrated as an appropriate delivery system for carrying cmvNT-3-HRE to the brain for ICH therapy. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:9717 / 9727
页数:11
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