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嵌合小鼠角膜缘上皮干细胞中性漂移的计算机模拟

Computer simulation of neutral drift among limbal epithelial stem cells of mosaic mice.

作者信息

West John D, Mort Richard L, Hill Robert E, Morley Steven D, Collinson J Martin

机构信息

Centre for Integrative Physiology, University of Edinburgh Medical School, Hugh Robson Building, George Square, Edinburgh EH8 9XD, UK.

Division of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Bailrigg, Lancaster LA1 4YG, UK.

出版信息

Stem Cell Res. 2018 Jul;30:1-11. doi: 10.1016/j.scr.2018.05.003. Epub 2018 May 13.

Abstract

The use of mice that are mosaic for reporter gene expression underlies many lineage-tracing studies in stem cell biology. For example, using mosaic LacZ reporter mice, it was shown that limbal epithelial stem cells (LESCs) around the periphery of the cornea maintain radial sectors of the corneal epithelium and that radial stripe numbers declined with age. Originally, the corneal results were interpreted as progressive, age-related loss or irreversible inactivation of some LESC clones. In this study we used computer simulations to show that these results could also be explained by stochastic replacement of LESCs by neighbouring LESCs, leading to neutral drift of LESC populations. This was shown to reduce the number of coherent clones of LESCs and hence would coarsen the mosaic pattern in the corneal epithelium without reducing the absolute number of LESCs. Simulations also showed that corrected stripe numbers declined more slowly when LESCs were grouped non-randomly and that mosaicism was rarely lost unless simulated LESC numbers were unrealistically low. Possible reasons why age-related changes differ between mosaic corneal epithelia and other systems, such as adrenal cortices and intestinal crypts, are discussed.

摘要

在干细胞生物学的许多谱系追踪研究中,都使用了报告基因表达呈嵌合状态的小鼠。例如,利用嵌合LacZ报告基因小鼠,研究表明角膜周边的角膜缘上皮干细胞(LESC)维持角膜上皮的放射状区域,且放射状条纹数量随年龄增长而减少。最初,角膜研究结果被解释为某些LESC克隆的渐进性、与年龄相关的丢失或不可逆失活。在本研究中,我们使用计算机模拟表明,这些结果也可以通过相邻LESC对LESC的随机替代来解释,从而导致LESC群体的中性漂移。结果表明,这会减少LESC的连贯克隆数量,进而使角膜上皮中的嵌合模式变得粗糙,而不会减少LESC的绝对数量。模拟还表明,当LESC非随机分组时,校正后的条纹数量下降得更慢,并且除非模拟的LESC数量低到不现实的程度,否则嵌合状态很少会丢失。我们还讨论了嵌合角膜上皮与其他系统(如肾上腺皮质和肠隐窝)之间与年龄相关的变化存在差异的可能原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4430/6049397/5b772d1058cc/gr2.jpg

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