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利用谱系追踪研究肾脏损伤和再生。

The use of lineage tracing to study kidney injury and regeneration.

机构信息

Excellence Centre for Research, Transfer and High Education for the development of DE NOVO Therapies (DENOTHE), University of Florence, Viale Pieraccini 6, 50139 Florence, Italy.

Stanford Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

出版信息

Nat Rev Nephrol. 2015 Jul;11(7):420-31. doi: 10.1038/nrneph.2015.67. Epub 2015 May 12.

Abstract

Lineage tracing is a powerful tool to track cells in vivo and provides enhanced spatial, temporal, and kinetic resolution of the mechanisms that underlie tissue renewal and repair. The data obtained from novel mouse models engineered for lineage tracing has started to transform our understanding of the changes in cell fate that underlie renal pathophysiology, the role of stem and/or progenitor cells in kidney development, and the mechanisms of kidney regeneration. The complexity of the genetic systems that are engineered for lineage tracing requires careful analysis and interpretation. In this Review we emphasize that close attention in lineage tracing studies must be paid to the specificity of the promoter, the use of drug-controlled activation of Cre recombinase as a genetic switch, and the type of reporter that should be engineered into lineage tracing genetic constructs. We evaluate the optimal experimental conditions required to achieve the pre-specified aims of the study and discuss the novel genetic techniques that are becoming available to study putative renal progenitor cells and the mechanisms of kidney regeneration.

摘要

谱系追踪是一种强大的工具,可以在体内追踪细胞,并提供对组织更新和修复背后机制的增强的空间、时间和动力学分辨率。从新型用于谱系追踪的小鼠模型中获得的数据开始改变我们对肾脏病理生理学中细胞命运变化、干细胞和/或祖细胞在肾脏发育中的作用以及肾脏再生机制的理解。用于谱系追踪的遗传系统的复杂性需要仔细分析和解释。在这篇综述中,我们强调在谱系追踪研究中必须密切注意启动子的特异性、使用药物控制 Cre 重组酶的激活作为遗传开关以及应该设计到谱系追踪遗传构建体中的报告基因类型。我们评估了实现研究预定目标所需的最佳实验条件,并讨论了用于研究潜在肾祖细胞和肾脏再生机制的新型遗传技术。

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