Schwann cell delivery of neurotrophic factors for peripheral nerve regeneration

被引:172
作者
Madduri, Srinivas [1 ]
Gander, Bruno [1 ]
机构
[1] ETH, Inst Pharmaceut Sci, CH-8093 Zurich, Switzerland
关键词
adenoviral vector; cellular delivery; nerve conduits; nerve regeneration; neurotrophic factors; Schwann cells; Schwann cell transduction; DEPENDENT ADENOVIRUS VECTOR; OLFACTORY ENSHEATHING CELLS; FIBROBLAST-GROWTH-FACTOR; EFFECTIVE GENE-TRANSFER; IN-VITRO; NEURITE OUTGROWTH; ENHANCES REGENERATION; NONNEURONAL CELLS; SUSTAINED-RELEASE; SILICONE CHAMBERS;
D O I
10.1111/j.1529-8027.2010.00257.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Current treatments of injured peripheral nerves often fail to mediate satisfactory functional recovery. For axonal regeneration, neurotrophic factors (NTFs) play a crucial role. Multiple NTFs and other growth-promoting factors are secreted, amongst others, by Schwann cells (SCs), which also provide cellular guidance for regenerating axons. Therefore, delivery of NTFs and transplantation of autologous or genetically modified SCs with therapeutic protein expression have been proposed. This article reviews polymer-based and cellular approaches for NTF delivery, with a focus on SCs and strategies to modulate SC gene expression. Polymer-based NTF delivery has mostly resided on nerve conduits (NC). While NC have generally provided prolonged NTF release, their therapeutic effect has remained significantly below that achieved with autologous nerve grafts. Several studies demonstrated enhanced nerve regeneration using NC seeded with SCs. The SCs have sometimes been modified genetically using non-viral or viral vectors. Whereas non-viral vectors produced poor transgene delivery, adenoviral vectors mediated high transgene transduction efficiency of SCs. Further improvements of safety and transgene expression of adenoviral vector may lead to rapid translation of pre-clinical research to clinical trials.
引用
收藏
页码:93 / 103
页数:11
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