Department of Orthopaedic Surgery, National Defense Medical College, Saitama, Japan.
PLoS One. 2010 Sep 28;5(9):e13034. doi: 10.1371/journal.pone.0013034.
Gene transduction has been considered advantageous for the sustained delivery of proteins to specific target tissues. However, in the case of hard tissues, such as bone, local gene delivery remains problematic owing to anatomical accessibility limitations of the target sites.
METHODOLOGY/PRINCIPAL FINDINGS: Here, we evaluated the feasibility of exogenous gene transduction in the interior of bone via axonal transport following intramuscular administration of a nonviral vector. A high expression level of the transduced gene was achieved in the tibia ipsilateral to the injected tibialis anterior muscle, as well as in the ipsilateral sciatic nerve and dorsal root ganglia. In sciatic transection rats, the gene expression level was significantly lowered in bone.
CONCLUSIONS/SIGNIFICANCE: These results suggest that axonal transport is critical for gene transduction. Our study may provide a basis for developing therapeutic methods for efficient gene delivery into hard tissues.
基因转导被认为有利于将蛋白质持续递送到特定的靶组织。然而,在硬组织(如骨骼)的情况下,由于靶部位的解剖可及性限制,局部基因传递仍然存在问题。
方法/主要发现:在这里,我们通过肌肉内给予非病毒载体,评估了经轴突运输将外源性基因递送至骨内的可行性。在注射的胫骨前肌同侧的胫骨以及同侧的坐骨神经和背根神经节中,实现了转导基因的高表达水平。在坐骨神经横断大鼠中,骨内的基因表达水平显著降低。
结论/意义:这些结果表明,轴突运输对基因转导至关重要。我们的研究可能为开发高效将基因递送至硬组织的治疗方法提供基础。