首页> 美国卫生研究院文献>Journal of Neural Transplantation >Cortical AAV-CNTF Gene Therapy Combined with Intraspinal Mesenchymal Precursor Cell Transplantation Promotes Functional and Morphological Outcomes after Spinal Cord Injury in Adult Rats
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Cortical AAV-CNTF Gene Therapy Combined with Intraspinal Mesenchymal Precursor Cell Transplantation Promotes Functional and Morphological Outcomes after Spinal Cord Injury in Adult Rats

机译:皮质AAV-CNTF基因疗法联合脊髓内间充质前体细胞移植促进成年大鼠脊髓损伤后的功能和形态学结果。

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摘要

Ciliary neurotrophic factor (CNTF) promotes survival and enhances long-distance regeneration of injured axons in parts of the adult CNS. Here we tested whether CNTF gene therapy targeting corticospinal neurons (CSN) in motor-related regions of the cerebral cortex promotes plasticity and regrowth of axons projecting into the female adult F344 rat spinal cord after moderate thoracic (T10) contusion injury (SCI). Cortical neurons were transduced with a bicistronic adeno-associated viral vector (AAV1) expressing a secretory form of CNTF coupled to mCHERRY (AAV-CNTFmCherry) or with control AAV only (AAV-GFP) two weeks prior to SCI. In some animals, viable or nonviable F344 rat mesenchymal precursor cells (rMPCs) were injected into the lesion site two weeks after SCI to modulate the inhibitory environment. Treatment with AAV-CNTFmCherry, as well as with AAV-CNTFmCherry combined with rMPCs, yielded functional improvements over AAV-GFP alone, as assessed by open-field and Ladderwalk analyses. Cyst size was significantly reduced in the AAV-CNTFmCherry plus viable rMPC treatment group. Cortical injections of biotinylated dextran amine (BDA) revealed more BDA-stained axons rostral and alongside cysts in the AAV-CNTFmCherry versus AAV-GFP groups. After AAV-CNTFmCherry treatments, many sprouting mCherry-immunopositive axons were seen rostral to the SCI, and axons were also occasionally found caudal to the injury site. These data suggest that CNTF has the potential to enhance corticospinal repair by transducing parent CNS populations.
机译:睫状神经营养因子(CNTF)可以提高成年中枢神经系统部分患者的存活率,并促进受损轴突的远距离再生。在这里,我们测试了针对中枢性胸部(T10)挫伤性损伤(SCI)的成年F344大鼠成年雌鼠脊髓中,针对大脑皮层运动相关区域的皮质脊髓神经元(CSN)的CNTF基因疗法是否促进了轴突的可塑性和再生。皮质神经元在两周前用双顺反子腺相关病毒载体(AAV1)转导,其表达分泌形式的CNTF与mCHERRY偶联(AAV-CNTF mCherry ),或仅与对照AAV(AAV-GFP)结合到SCI。在某些动物中,在SCI后两周将有活力或无活力的F344大鼠间充质前体细胞(rMPC)注入病变部位,以调节抑制环境。 AAV-CNTF mCherry 以及AAV-CNTF mCherry 结合rMPC的治疗,与单独的AAV-GFP相比,功能得到了改善,如通过开放视野和Ladderwalk评估分析。 AAV-CNTF mCherry 加可行的rMPC治疗组的囊肿大小明显减少。皮层注射生物素化的右旋糖酐胺(BDA)与AAV-GFP组相比,在AAV-CNTF 组中,BDA染色的轴突和囊肿有更多。经过AAV-CNTF mCherry 处理后,发现许多发芽的mCherry免疫阳性轴突位于SCI的鼻端,并且偶尔在损伤部位尾部也发现了轴突。这些数据表明,CNTF具有通过转导亲本CNS群体来增强皮质脊髓修复的潜力。

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