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Direct reprogramming of somatic cells is promoted by maternal transcription factor Glis1.母体转录因子 Glis1 促进体细胞的直接重编程。
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Rescue of ATP7B function in hepatocyte-like cells from Wilson's disease induced pluripotent stem cells using gene therapy or the chaperone drug curcumin.使用基因治疗或伴侣药物姜黄素挽救肝样细胞中威尔逊病诱导多能干细胞中的 ATP7B 功能。
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基因治疗:对颅面再生的影响。

Gene therapy: implications for craniofacial regeneration.

作者信息

Scheller Erica L, Villa-Diaz Luis G, Krebsbach Paul H

机构信息

Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, Michigan 48109-1078, USA.

出版信息

J Craniofac Surg. 2012 Jan;23(1):333-7. doi: 10.1097/SCS.0b013e318241dc11.

DOI:10.1097/SCS.0b013e318241dc11
PMID:22337437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3282143/
Abstract

Gene therapy in the craniofacial region provides a unique tool for delivery of DNA to coordinate protein production in both time and space. The drive to bring this technology to the clinic is derived from the fact that more than 85% of the global population may at one time require repair or replacement of a craniofacial structure. This need ranges from mild tooth decay and tooth loss to temporomandibular joint disorders and large-scale reconstructive surgery. Our ability to insert foreign DNA into a host cell has been developing since the early uses of gene therapy to alter bacterial properties for waste cleanup in the 1980s followed by successful human clinical trials in the 1990s to treat severe combined immunodeficiency. In the past 20 years, the emerging field of craniofacial tissue engineering has adopted these techniques to enhance regeneration of mineralized tissues, salivary gland, and periodontium and to reduce tumor burden of head and neck squamous cell carcinoma. Studies are currently pursuing research on both biomaterial-mediated gene delivery and more clinically efficacious, although potentially more hazardous, viral methods. Although hundreds of gene therapy clinical trials have taken place in the past 20 years, we must still work to ensure an ideal safety profile for each gene and delivery method combination. With adequate genotoxicity testing, we can expect gene therapy to augment protein delivery strategies and potentially allow for tissue-specific targeting, delivery of multiple signals, and increased spatial and temporal control with the goal of natural tissue replacement in the craniofacial complex.

摘要

颅面部区域的基因治疗为DNA传递提供了一种独特的工具,可在时间和空间上协调蛋白质的产生。将这项技术应用于临床的动力源于这样一个事实,即全球超过85%的人口可能在某个时候需要修复或替换颅面部结构。这种需求范围从轻微的蛀牙和牙齿脱落到颞下颌关节紊乱以及大规模的重建手术。自20世纪80年代基因治疗早期用于改变细菌特性以进行废物清理,随后在90年代成功进行人类临床试验以治疗严重联合免疫缺陷以来,我们将外源DNA插入宿主细胞的能力一直在不断发展。在过去20年中,颅面部组织工程这一新兴领域采用了这些技术来促进矿化组织、唾液腺和牙周组织的再生,并减轻头颈部鳞状细胞癌的肿瘤负担。目前的研究正在探索生物材料介导的基因传递以及更具临床疗效但可能更具危险性的病毒方法。尽管在过去20年中已经进行了数百项基因治疗临床试验,但我们仍必须努力确保每种基因与传递方法组合都具有理想的安全性。通过充分的基因毒性测试,我们可以期待基因治疗增强蛋白质传递策略,并有可能实现组织特异性靶向、多种信号的传递以及增强时空控制,目标是在颅面部复合体中实现天然组织替代。