Functionally competent eosinophils differentiated ex vivo in high purity from normal mouse bone marrow

KD Dyer, JM Moser, M Czapiga, SJ Siegel… - The Journal of …, 2008 - journals.aai.org
KD Dyer, JM Moser, M Czapiga, SJ Siegel, CM Percopo, HF Rosenberg
The Journal of Immunology, 2008journals.aai.org
We have devised an ex vivo culture system which generates large numbers of eosinophils at
high purity (> 90%) from unselected mouse bone marrow progenitors. In response to 4 days
of culture with recombinant mouse FLT3-L and recombinant mouse stem cell factor followed
by recombinant mouse IL-5 alone thereafter, the resulting bone marrow-derived eosinophils
(bmEos) express immunoreactive major basic protein, Siglec F, IL-5R α-chain, and
transcripts encoding mouse eosinophil peroxidase, CCR3, the IL-3/IL-5/GM-CSF receptor …
Abstract
We have devised an ex vivo culture system which generates large numbers of eosinophils at high purity (> 90%) from unselected mouse bone marrow progenitors. In response to 4 days of culture with recombinant mouse FLT3-L and recombinant mouse stem cell factor followed by recombinant mouse IL-5 alone thereafter, the resulting bone marrow-derived eosinophils (bmEos) express immunoreactive major basic protein, Siglec F, IL-5R α-chain, and transcripts encoding mouse eosinophil peroxidase, CCR3, the IL-3/IL-5/GM-CSF receptor common β-chain, and the transcription factor GATA-1. BmEos are functionally competent: they undergo chemotaxis toward mouse eotaxin-1 and produce characteristic cytokines, including IFN-γ, IL-4, MIP-1α, and IL-6. The rodent pathogen pneumonia virus of mice replicates in bmEos and elevated levels of IL-6 are detected in supernatants of bmEos cultures in response to active infection. Finally, differentiating bmEos are readily transfected with lentiviral vectors, suggesting a means for rapid production of genetically manipulated cells.
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