2014-11-26

Murine Ba/F3 Cell Line Is Helpful to the Selectivity of Kinase Inhibitor


Kinase inhibition is an area of significant interest across academia and pharmaceutical industry. However, discovering the full range of intracellular targets of a small molecule kinase inhibitor can be a daunting task. This information is needed to understand the mechanistic basis for potential toxicities and find out the particular inhibitor which tumors may respond to.

Besides the 518 known kinases encoded in the human genome, there are over 2,000 other nucleotide-dependent enzymes, including polymerases, chaperones, motor proteins, reductases and methyltransferases, possibly containing binding sites. Ideally, the selectivity of a new kinase inhibitor is evaluated at the level of the protein, cell and whole organism.

Cellular selectivity of kinase inhibitors can be evaluated by using panels of cell lines that are engineered to report on inhibition of a particular kinase or using unbiased proteomics approaches, and many such cell lines have been developed from the murine Ba/F3 cell line.

Murine Ba/F3 cell line is pro-B-cell line whose proliferation normally requires the cytokine interleukin 3 (IL-3). However, its transformation by an oncogenic kinase will lead to IL-3-independent proliferation and survival, and thus the rate of cell growth and proliferation can be used as a read-out of intracellular kinase inhibition. Further, cytotoxicity that results from specific kinase inhibition can be discriminated from non-specific cytotoxicity through the introduction of IL-3. Panels of kinase-transformed Ba/F3 cells can be created by using either naturally occurring oncogenic fusion proteins or by creating artificial fusions between kinase domains and domain Tel found in several naturally occurring fusion proteins with a strong ability to multimerize fused proteins.

Creative bioarray offers high quality murine Ba/F3 cells or cell line for research use. Its IL-3 dependent murine pro-B-cell line is found with a lymphatic back ground. Performing May-Grünwald-Giemsa staining provide the evidence that those cells are derived from C3H mouse.

You can get murine Ba/F3 cells at





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