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Delivery of Recombinant Adeno-Associated Virus Vectors to Rat Diaphragm Muscle via Direct Intramuscular Injection

机译:通过直接肌内注射将重组腺相关病毒载体传递到大鼠Dia肌

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摘要

The diaphragm is the most important inspiratory muscle in all mammals, and ventilatory insufficiency caused by diaphragm dysfunction is the leading cause of morbidity and mortality in many genetic and acquired diseases affecting skeletal muscle. Currently, pharmacological inhibitors, genetically modified animals, and invasive procedures are used to study disorders affecting the diaphragm. However, these methodologies can be problematic because of off-target drug effects and the possible nonphysiological consequences of lifelong genetic alterations. Therefore, alternative methods to study this important respiratory muscle are needed. To resolve this, we have developed a methodology to deliver recombinant adeno-associated virus (rAAV) vectors to the rat diaphragm via direct intramuscular injection. We hypothesized that by direct injection of rAAV into the muscle we can selectively target the diaphragm and establish a novel experimental method for studying signaling pathways and also provide a strategy for effectively using rAAV to protect the diaphragm against disease. This report describes the methods and evidence to support the use of rAAV as a therapeutic intervention to study rat diaphragm biology during conditions that promote diaphragm dysfunction.
机译:在所有哺乳动物中,all肌是最重要的吸气肌,而diaphragm肌功能障碍引起的通气功能不全是影响骨骼肌的许多遗传性和后天性疾病的发病率和死亡率的主要原因。当前,药理抑制剂,转基因动物和侵入性程序被用于研究影响affecting肌的疾病。但是,由于脱靶药物的作用以及终生遗传改变的可能的非生理后果,这些方法可能会出现问题。因此,需要替代的方法来研究这种重要的呼吸肌。为解决此问题,我们开发了一种通过直接肌肉内注射将重组腺相关病毒(rAAV)载体递送至大鼠diaphragm肌的方法。我们假设通过将rAAV直接注射到肌肉中,我们可以选择性地靶向隔膜,并建立一种研究信号通路的新型实验方法,并且还提供了有效使用rAAV保护隔膜免受疾病侵袭的策略。该报告描述了在促进diaphragm肌功能障碍的情况下支持将rAAV用作治疗大鼠biology肌生物学的治疗性干预措施的方法和证据。

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