Kohro Yuta, Sakaguchi Emi, Tashima Ryoichi, Tozaki-Saitoh Hidetoshi, Okano Hideyuki, Inoue Kazuhide, Tsuda Makoto
Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Department of Life Innovation, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Sci Rep. 2015 Sep 21;5:14306. doi: 10.1038/srep14306.
Noninvasive gene delivery to the spinal dorsal horn (SDH) remains challenging because existing methods to directly microinject vectors require laminectomy, which leads to tissue damage and inflammation. Such responses might hamper accurate readouts of cellular and behavioural effects of an introduced gene. Here we develop a new minimally-invasive SDH microinjection technique without the need of laminectomy in which a microcapillary is inserted into the SDH parenchyma through an intervertebral space. Using this method, we microinjected adeno-associated virus with an astrocytic promoter into the SDH and achieved efficient gene expression in an astrocyte-specific manner without gliosis, neuronal loss or inflammation. Furthermore, astrocytic loss- and gain-of-function of the transcription factor STAT3 by expressing a dominant-negative form and a constitutive-active form of STAT3, respectively, demonstrated the necessity and sufficiency of astrocytic STAT3 in the maintenance of neuropathic pain following peripheral nerve injury, a debilitating chronic pain state in which currently available treatments are frequently ineffective. Thus, our technique enables manipulation of gene expression in cell type- and spatial-specific manners without adverse effects, and may be useful for research in SDH physiology and pathology.
向脊髓背角(SDH)进行非侵入性基因递送仍然具有挑战性,因为现有的直接微量注射载体的方法需要进行椎板切除术,这会导致组织损伤和炎症。这种反应可能会妨碍对导入基因的细胞和行为效应进行准确的读数。在这里,我们开发了一种无需椎板切除术的新型微创SDH微量注射技术,其中通过椎间间隙将微毛细管插入SDH实质。使用这种方法,我们将带有星形胶质细胞启动子的腺相关病毒微量注射到SDH中,并以星形胶质细胞特异性方式实现了高效的基因表达,而没有胶质增生、神经元丢失或炎症。此外,分别通过表达STAT3的显性负性形式和组成型活性形式来实现转录因子STAT3在星形胶质细胞中的功能丧失和功能获得,证明了星形胶质细胞STAT3在维持周围神经损伤后神经性疼痛中的必要性和充分性,周围神经损伤是一种使人衰弱的慢性疼痛状态,目前可用的治疗方法常常无效。因此,我们的技术能够以细胞类型和空间特异性方式操纵基因表达而无不良影响,并且可能对SDH生理学和病理学研究有用。