Kone B C
Department of Internal Medicine, The University of Texas Medical School at Houston, 77030, USA.
Semin Nephrol. 1998 Mar;18(2):102-21.
The recent development of methods to transfer, mutate, or ablate genes in vivo has provided renal investigators and physicians with powerful tools to explore normal renal physiology, the pathophysiological basis of renal disease, and potential therapeutic interventions. The use of transgenic and knockout mice to produce gain-of-function and loss-of-function mutations, and to create animal models of human hereditary renal diseases, permits unprecedented versatility and power of experimental design. Conditional and inducible gene targeting methods to control the temporal and spatial expression of transgenes offer considerable promise in studying the impact of normal and disease genes in the kidney. In vivo gene transfer of encoding DNAs, antisense DNA and RNA, and cis-element decoys allows manipulation of specific genes in somatic cells. Liposome-mediated, virally mediated, and ex vivo transduced renal cells represent novel approaches to facilitate in vivo gene transfer to the kidney.
近年来,体内基因转移、突变或消融方法的发展为肾脏研究人员和医生提供了强大的工具,用于探索正常肾脏生理学、肾脏疾病的病理生理基础以及潜在的治疗干预措施。利用转基因小鼠和基因敲除小鼠产生功能获得性和功能丧失性突变,并创建人类遗传性肾脏疾病的动物模型,使得实验设计具有前所未有的通用性和强大功能。用于控制转基因时空表达的条件性和诱导性基因靶向方法,在研究正常和疾病基因对肾脏的影响方面具有巨大潜力。编码DNA、反义DNA和RNA以及顺式元件诱饵的体内基因转移,能够对体细胞中的特定基因进行操作。脂质体介导、病毒介导以及体外转导的肾细胞,代表了促进体内基因向肾脏转移的新方法。