Mechanisms and promotion of 3D neurite bridging between PHBV microspheres in a microsphere-hydrogel hybrid scaffold

被引:6
作者
Chen, Wenhui [2 ]
Tong, Yen Wah [1 ]
机构
[1] Natl Univ Singapore, Dept Biomol & Chem Engn, Singapore 117548, Singapore
[2] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore 117548, Singapore
关键词
CENTRAL-NERVOUS-SYSTEM; STEM-CELLS; IN-VITRO; MULTIPLE-SCLEROSIS; DRUG-DELIVERY; GROWTH-FACTOR; PC12; CELL; TISSUE; THERAPY; RELEASE;
D O I
10.1039/c1sm06473h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) microspheres have been previously found to support the proliferation and differentiation of a variety of neuronal cells; however, to establish functional neural networks and tissue integration, the cells on the microspheres have to be connected. It was found that neurites bridged the microspheres but these connections were fragile. Thus, the neurons on PHBV microspheres (neuron-microspheres) were encapsulated in a laminin-collagen hydrogel to promote and protect the bridging formations. Bridges were found across the continuous surface between microspheres in contact (surface bridges), and in the gel space between microspheres (suspended bridges). This neuron-microsphere-hydrogel construct increased the proportion of bridge-forming neurites by 31% as compared to neuron-microspheres alone. Furthermore, the neuron-microsphere-hydrogel was found to increase the proportion of suspended bridges by 3.5 times. The surface bridges were subsequently verified to form from neurites extending across continuous surfaces, and thus packing microspheres closer to generate more continuous surfaces increased surface bridging by 70%. However, seeding cells into the gel space did not increase the proportion of suspended bridges but this still increased the overall proportion of bridges by 21%. Images of neurites in the gel space suggested that suspended bridges could have formed instead from neurites extending out of microsphere surfaces into the gel space. This is the first study to focus on neurite bridging and microspheres as scaffolds supported by hydrogel. Furthermore, a novel neurite guidance cue was found in the form of continuous surfaces.
引用
收藏
页码:11372 / 11379
页数:8
相关论文
共 50 条
[1]   Delivering neuroactive molecules from biodegradable microspheres for application in central nervous system disorders [J].
Cao, XD ;
Shoichet, MS .
BIOMATERIALS, 1999, 20 (04) :329-339
[2]   From stem cells to oligodendrocytes: Prospects for brain therapy [J].
Chen, Cui P. ;
Kiel, Mary E. ;
Sadowski, Dorota ;
McKinnon, Randall D. .
STEM CELL REVIEWS, 2007, 3 (04) :280-288
[3]   The release of diazepam from poly(hydroxybutyrate-hydroxyvalerate) microspheres [J].
Chen, J ;
Davis, SS .
JOURNAL OF MICROENCAPSULATION, 2002, 19 (02) :191-201
[4]   PHBV microspheres as neural tissue engineering scaffold support neuronal cell growth and axon-dendrite polarization [J].
Chen, Wenhui ;
Tong, Yen Wah .
ACTA BIOMATERIALIA, 2012, 8 (02) :540-548
[5]   Fabricating Tissue Engineering Scaffolds for Simultaneous Cell Growth and Drug Delivery [J].
Chen, Wenhui ;
Tabata, Yasuhiko ;
Tong, Yen Wah .
CURRENT PHARMACEUTICAL DESIGN, 2010, 16 (21) :2388-2394
[6]   Production of neurons, astrocytes and oligodendrocytes from mammalian CNS stem cells [J].
Chojnacki, Andrew ;
Weiss, Samuel .
NATURE PROTOCOLS, 2008, 3 (06) :935-940
[7]   Surface engineered and drug releasing pre-fabricated scaffolds for tissue engineering [J].
Chung, Hyun Jung ;
Park, Tae Gwan .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (4-5) :249-262
[8]   Treatments for spinal cord injury: Is there hope in neurosteroids? [J].
Compagnone, Nathahe A. .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2008, 109 (3-5) :307-313
[9]   Progesterone neuroprotection in traumatic CNS injury and motoneuron degeneration [J].
De Nicola, Alejandro F. ;
Labombarda, Florencia ;
Gonzalez Deniselle, Maria Claudia ;
Gonzalez, Susana L. ;
Garay, Laura ;
Meyer, Maria ;
Gargiulo, Gisella ;
Guennoun, Rachida ;
Schumacher, Michael .
FRONTIERS IN NEUROENDOCRINOLOGY, 2009, 30 (02) :173-187
[10]  
Dehmelt L, 2005, GENOME BIOL, V6