Chamberlain Joel R, Schwarze Ulrike, Wang Pei-Rong, Hirata Roli K, Hankenson Kurt D, Pace James M, Underwood Robert A, Song Kit M, Sussman Michael, Byers Peter H, Russell David W
Department of Medicine, University of Washington, Seattle, WA 98195-7720, USA.
Science. 2004 Feb 20;303(5661):1198-201. doi: 10.1126/science.1088757.
Adult stem cells offer the potential to treat many diseases through a combination of ex vivo genetic manipulation and autologous transplantation. Mesenchymal stem cells (MSCs, also referred to as marrow stromal cells) are adult stem cells that can be isolated as proliferating, adherent cells from bones. MSCs can differentiate into multiple cell types present in several tissues, including bone, fat, cartilage, and muscle, making them ideal candidates for a variety of cell-based therapies. Here, we have used adeno-associated virus vectors to disrupt dominant-negative mutant COL1A1 collagen genes in MSCs from individuals with the brittle bone disorder osteogenesis imperfecta, demonstrating successful gene targeting in adult human stem cells.
成体干细胞通过体外基因操作和自体移植相结合的方式,为治疗多种疾病提供了可能。间充质干细胞(MSCs,也称为骨髓基质细胞)是一种成体干细胞,可以从骨骼中分离出具有增殖能力、贴壁生长的细胞。间充质干细胞能够分化为多种组织中的多种细胞类型,包括骨骼、脂肪、软骨和肌肉,这使其成为多种基于细胞的治疗方法的理想候选者。在此,我们使用腺相关病毒载体来破坏患有脆性骨病成骨不全症个体的间充质干细胞中显性负性突变COL1A1胶原蛋白基因,证明了在成人干细胞中成功进行基因靶向。