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.
引用
收藏
页码:9717 / 9727
页数:11
相关论文
共 49 条
[11]   Differential effects of hypoxia on untreated and NGF treated PC12 cells [J].
Gross, J ;
Leclere, N ;
Heldt, J ;
Müller, I ;
Kietzmann, T ;
Andreeva, N .
LIFE SCIENCES, 2000, 67 (21) :2595-2603
[12]   Effects of hypoxia on endothelial/pericytic co-culture model of the blood-brain barrier [J].
Hayashi, K ;
Nakao, S ;
Nakaoke, R ;
Nakagawa, S ;
Kitagawa, N ;
Niwa, M .
REGULATORY PEPTIDES, 2004, 123 (1-3) :77-83
[13]   Neurotrophin production in brain pericytes during hypoxia: A role of pericytes for neuroprotection [J].
Ishitsuka, Koji ;
Ago, Tetsuro ;
Arimura, Koichi ;
Nakamura, Kuniyuki ;
Tokami, Himiko ;
Makihara, Noriko ;
Kuroda, Junya ;
Kamouchi, Masahiro ;
Kitazono, Takanari .
MICROVASCULAR RESEARCH, 2012, 83 (03) :352-359
[14]   Neurotrophin-3 administration alters neurotrophin, neurotrophin receptor and nestin mRNA expression in rat dorsal root ganglia following axotomy [J].
Kuo, L.-T. ;
Groves, M. J. ;
Scaravilli, F. ;
Sugden, D. ;
An, S. F. .
NEUROSCIENCE, 2007, 147 (02) :491-507
[15]   Loading efficiency of stavudine on polybutylcyanoacrylate and methylmethaerylate-sulfopropylmethacrylate copolymer nanoparticles [J].
Kuo, YC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 290 (1-2) :161-172
[16]   Guided differentiation of induced pluripotent stem cells into neuronal lineage in alginate-chitosan-gelatin hydrogels with surface neuron growth factor [J].
Kuo, Yung-Chih ;
Wang, Cheng-Chin .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2013, 104 :194-199
[17]   Accelerated nerve regeneration using induced pluripotent stem cells in chitin-chitosan-gelatin scaffolds with inverted colloidal crystal geometry [J].
Kuo, Yung-Chih ;
Lin, Ching-Chun .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2013, 103 :595-600
[18]   Inverted colloidal crystal scaffolds with induced pluripotent stem cells for nerve tissue engineering [J].
Kuo, Yung-Chih ;
Chen, Chun-Wei .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2013, 102 :789-794
[19]   TATVHL peptide-grafted alginate/poly(γ-glutamic acid) scaffolds with inverted colloidal crystal topology for neuronal differentiation of iPS cells [J].
Kuo, Yung-Chih ;
Chung, Chiu-Yen .
BIOMATERIALS, 2012, 33 (35) :8955-8966
[20]   Material-driven differentiation of induced pluripotent stem cells in neuron growth factor-grafted poly(ε-caprolactone)-poly(β-hydroxybutyrate) scaffolds [J].
Kuo, Yung-Chih ;
Huang, Min-Jung .
BIOMATERIALS, 2012, 33 (23) :5672-5682