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Microwell arrays reveal cellular heterogeneity during the clonal expansion of transformed human cells.
Chang, Tim C; Tang, Weiliang; Koh, William Jen Hoe; Rettie, Alexander J E; Emond, Mary J; Monnat, Raymond J; Folch, Albert.
Afiliação
  • Chang TC; Departments of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Tang W; Departments of Pathology, University of Washington, Seattle, WA 98195, USA.
  • Koh WJ; Departments of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Rettie AJ; Departments of Bioengineering, University of Washington, Seattle, WA 98195, USA.
  • Emond MJ; Departments of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Monnat RJ; Departments of Pathology, University of Washington, Seattle, WA 98195, USA; Departments of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
  • Folch A; Departments of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Technology (Singap World Sci) ; 3(4): 163-171, 2015 Dec.
Article em En | MEDLINE | ID: mdl-27158641
ABSTRACT
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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article