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Adenovirus-mediated gene transfer of Bcl-xL prevents cell death in primary neuronal culture of the rat
Authors:Norihiro Matsuoka   Hiroyuki Yukawa   Kazuhiro Ishii   Hirofumi Hamada   Masayuki Akimoto   Nobuo Hashimoto  Shin-Ichi Miyatake  
Affiliation:

a Department of Neurosurgery and Clinical Neuroscience, Faculty of Medicine, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606–8507, Japan

b Institute for Virus Research, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606–8507, Japan

c Department of Molecular Biotherapy Research, Cancer Chemotherapy Center, Cancer Institute, 1–37–1, Kami-Ikebukuro, Toshima-ku, Tokyo, Japan

d Department of Ophthalmology, Shinshu University, 3–1–1, Asahi, Matsumoto, Nagano, 390–0802, Japan

Abstract:
Bcl-xL is a Bcl-2-related gene that regulates programmed cell death in a bcl-2-independent fashion. It is expressed in tissues containing long-surviving postmitotic cells, such as neurons in adult brains. To investigate the possibility of gene therapy for transferring this anti-apoptotic gene into the neuron for the treatment of vascular occlusive or neurodegenerative diseases, we examined the effect of a replication-deficient recombinant adenovirus vector coding human Bcl-xL gene on the augmentation of the survival of primarily-cultured rat neuronal cells in vitro. Immunoblot analysis revealed that primarily-cultured neuronal cells were successfully infected and transferred with this gene by recombinant adenovirus vector with high transduction efficiency. Bcl-xL gene transfer to the primarily-cultured neurons could prevent these cells from cell death.
Keywords:Adenovirus   Apoptosis   Bcl-xL   Gene transfer   Neuronal cell death   Primary neuronal culture
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