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A new in vitro model for stem cell differentiation and interaction. | LitMetric

AI Article Synopsis

  • - Development of organisms involves complex interactions between various cell types, from their creation to their eventual specialization or death, which are crucial for understanding new organism formation.
  • - A model using embryoid bodies (EBs) from mouse embryonic stem cells has been developed to visualize the differentiation of cells and allows targeted removal of specific cell populations through an enzyme-prodrug system.
  • - Validation of the model includes demonstrating successful expression changes and apoptosis in Cre-expressing endothelial cells, showcasing its adaptability for studying various cell types with specific promoters.

Article Abstract

Development involves an interplay between various cell types from their birth to their disappearance by differentiation, migration, or death. Analyzing these interactions provides insights into their roles during the formation of a new organism. As a study tool for these interactions, we have created a model based on embryoid bodies (EBs) generated from mouse embryonic stem (mES) cells, which can be used to visualize the differentiation of mES cells into specific cell types while at the same time allowing controlled removal of this same cell population using an enzyme-prodrug approach. Cell-specific expression of Cre induces a switch of EGFP expression to LacZ. Furthermore, it leads to the expression of nitroreductase (NTR), which in combination with the prodrug CB1954 induces apoptosis. Here, we validate this model by showing expression of LacZ and NTR after Cre-mediated recombination. Additionally we show, as an example, that we can target the endothelial cells in EBs using the Tie-2 promoter driving Cre. Ablating Cre-expressing cells by adding CB1954 to the culture led to an abrogated vascular formation. This system can easily be adapted to determine the fate and interaction of many different cell types provided that there is a cell-type-specific promoter available.

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Source
http://dx.doi.org/10.1016/j.scr.2008.10.002DOI Listing

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