Hsu Mu-Nung, Liao Han-Tsung, Truong Vu Anh, Huang Kai-Lun, Yu Fu-Jen, Chen Hwei-Hsien, Nguyen Thi Kieu Nuong, Makarevich Pavel, Parfyonova Yelena, Hu Yu-Chen
Department of Chemical Engineering, National Tsing Hua University, Hsinchu, Taiwan, 300.
Department of Plastic and Reconstructive Surgery, Craniofacial Research Center, Chang Gung Memorial Hospital, Linkou, Taiwan, 333.
Theranostics. 2019 Aug 14;9(21):6099-6111. doi: 10.7150/thno.36790. eCollection 2019.
: Peripheral nerve regeneration requires coordinated functions of neurotrophic factors and neuronal cells. CRISPR activation (CRISPRa) is a powerful tool that exploits inactive Cas9 (dCas9), single guide RNA (sgRNA) and transcription activator for gene activation, but has yet to be harnessed for tissue regeneration. : We developed a hybrid baculovirus (BV) vector to harbor and deliver the CRISPRa system for multiplexed activation of 3 neurotrophic factor genes (, and ). The hybrid BV was used to transduce rat adipose-derived stem cells (ASC) and functionalize the ASC sheets. We further implanted the ASC sheets into sciatic nerve injury sites in rats. : Transduction of rat ASC with the hybrid BV vector enabled robust, simultaneous and prolonged activation of the 3 neurotrophic factors for at least 21 days. The CRISPRa-engineered ASC sheets were able to promote Schwann cell (SC) migration, neuron proliferation and neurite outgrowth . The CRISPRa-engineered ASC sheets further enhanced functional recovery, nerve reinnervation, axon regeneration and remyelination. : These data collectively implicated the potentials of the hybrid BV-delivered CRISPRa system for multiplexed activation of endogenous neurotrophic factor genes in ASC sheets to promote peripheral nerve regeneration.
周围神经再生需要神经营养因子和神经元细胞的协同作用。CRISPR激活(CRISPRa)是一种利用无活性Cas9(dCas9)、单向导RNA(sgRNA)和转录激活因子进行基因激活的强大工具,但尚未用于组织再生。
我们开发了一种杂交杆状病毒(BV)载体,用于携带和递送CRISPRa系统,以多重激活3个神经营养因子基因(、和)。杂交BV用于转导大鼠脂肪来源干细胞(ASC)并使ASC片功能化。我们进一步将ASC片植入大鼠坐骨神经损伤部位。
用杂交BV载体转导大鼠ASC能够强大、同时且长时间激活这3个神经营养因子至少21天。经CRISPRa工程改造的ASC片能够促进雪旺细胞(SC)迁移、神经元增殖和神经突生长。经CRISPRa工程改造的ASC片进一步增强了功能恢复、神经再支配、轴突再生和髓鞘再生。
这些数据共同表明,杂交BV递送的CRISPRa系统在多重激活ASC片中内源性神经营养因子基因以促进周围神经再生方面具有潜力。