微孔阵列揭示了转化人细胞克隆扩增过程中的细胞异质性。

Tim C Chang, Weiliang Tang, William Jen Hoe Koh, Alexander J E Rettie, Mary J Emond, Raymond J Monnat, Albert Folch
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引用次数: 6

摘要

我们开发了微成型微孔阵列来研究单细胞的增殖和衰老。微孔阵列被设计成与传统的细胞培养方案兼容,以简化细胞装载、细胞培养和成像。我们通过测量表达或已经耗尽人类维尔纳综合征蛋白的等基因细胞的增殖和衰老来证明这些阵列的实用性。我们的研究结果揭示了WRN+和WRN缺失成纤维细胞在克隆生长过程中增殖的细胞间异质性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.

Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.

Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.

Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.

We developed micromolded microwell arrays to study the proliferation and senescence of single cells. Microwell arrays were designed to be compatible with conventional cell culture protocols to simplify cell loading, cell culture, and imaging. We demonstrated the utility of these arrays by measuring the proliferation and senescence of isogenic cells which expressed or had been depleted of the human Werner syndrome protein. Our results allowed us to reveal cell-to-cell heterogeneity in proliferation in WRN+ and WRN-depleted fibroblasts during clonal growth.

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来源期刊
TECHNOLOGY
TECHNOLOGY ENGINEERING, MULTIDISCIPLINARY-
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