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基因、干细胞与生物起搏器。

Genes, stem cells and biological pacemakers.

作者信息

Rosen Michael R, Brink Peter R, Cohen Ira S, Robinson Richard B

机构信息

Center for Molecular Therapeutics, Deparment of Pharmacology, Columbia University, New York, NY 10032, USA.

出版信息

Cardiovasc Res. 2004 Oct 1;64(1):12-23. doi: 10.1016/j.cardiores.2004.05.012.

Abstract

The advent of gene therapy and cell therapy has led to reconsideration of standard therapies for cardiac disease. One such area of reconsideration is that of the cardiac pacemaker, which has been the mainstay of treatment for high-degree heart block and sinoatrial node dysfunction. Over the past five years, gene therapy has been used to explore the overexpression of beta(2)-adrenergic receptors, the down-regulation of inward rectifier current, and the overexpression of pacemaker current as potential sources of biological pacemakers. Cell therapy approaches have explored the "forcing" of embryonic stem cells to evolve along cardiac (and specifically pacemaker) cell lines and the use of adult mesenchymal stem cells as platforms for delivery of specific gene therapies. This review considers the strengths and weaknesses of each of the approaches used to date and attempts to look to the future of biological alternatives to electronic pacemakers.

摘要

基因治疗和细胞治疗的出现促使人们重新审视心脏病的标准疗法。其中一个重新审视的领域是心脏起搏器,它一直是治疗高度房室传导阻滞和窦房结功能障碍的主要手段。在过去五年中,基因治疗已被用于探索β(2)-肾上腺素能受体的过表达、内向整流电流的下调以及起搏电流的过表达,将其作为生物起搏器的潜在来源。细胞治疗方法则探索了促使胚胎干细胞沿着心脏(特别是起搏细胞)细胞系进化,以及利用成体间充质干细胞作为特定基因治疗的递送平台。本综述考虑了迄今为止所使用的每种方法的优缺点,并试图展望电子起搏器生物替代物的未来。

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