As part of our larger interest in eosinophils and their interactions with respiratory virus pathogens, we have developed a novel culture system which has permitted us to generate large numbers of eosinophils at high purity (>90%) from unselected mouse bone marrow progenitors. In response to four days of culture with recombinant mouse (rm)FLT3-L and rmSCF followed by rmIL-5 alone thereafter, the resulting bone-marrow derived eosinophils (bmEos) express immunoreactive major basic protein, Siglec F, IL-5 receptor alpha chain, and transcripts encoding mouse eosinophil peroxidase, CC chemokine receptor 3, the IL-3/IL-5/GM-CSF receptor common beta-chain (βc), and the transcription factor GATA-1. BmEos are functionally competent: they undergo chemotaxis toward mouse eotaxin-1 and produce characteristic cytokines, including interferon-γ, IL-4, MIP-1α and IL-6. Using this novel system, we found that the natural rodent pathogen, pneumonia virus of mice (PVM) 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 (Dyer et al., J Immunol. in press). ? ? I also contributed to three significant reviews. The first was a large, comprehensive review of eosinophil biology entitled """"""""Eosinophils: biological properties and role in health and disease"""""""" (Clin Exp Allergy, 2008; 38: 709 - 750). I also co-authored a review on the targeting eosinophils for future anti-asthma therapeutics (Current Molecular Medicine, 2008, in press) and an invited review featuring our work on interactions of eosinophils with respiratory virus pathogens (Immunologic Research, 2008, in press). ? ? Finally, my expertise in eosinophil biology and inflammation has provided me with the opportunity to participate as a member of the Editorial Boards of Blood (since 2003), Journal of Leukocyte Biology (since 1996; promoted to Associate Editor, 2006), Clinical and Vaccine Immunology (since 2003) and Faculty of 1000 Biology (since 2006).

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000941-05
Application #
7732596
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
2008
Total Cost
$736,753
Indirect Cost
City
State
Country
United States
Zip Code
Foster, Paul S; Maltby, Steven; Rosenberg, Helene F et al. (2017) Modeling TH 2 responses and airway inflammation to understand fundamental mechanisms regulating the pathogenesis of asthma. Immunol Rev 278:20-40
Percopo, Caroline M; Brenner, Todd A; Ma, Michelle et al. (2017) SiglecF+Gr1hi eosinophils are a distinct subpopulation within the lungs of allergen-challenged mice. J Leukoc Biol 101:321-328
Kraemer, Laura S; Brenner, Todd A; Krumholz, Julia O et al. (2017) A flow-cytometric method to evaluate eosinophil-mediated uptake of probiotic Lactobacillus reuteri. J Microbiol Methods 137:19-24
Rosenberg, Helene F; Druey, Kirk M (2016) Eosinophils, galectins, and a reason to breathe. Proc Natl Acad Sci U S A 113:9139-41
Rosenberg, Helene F; Masterson, Joanne C; Furuta, Glenn T (2016) Eosinophils, probiotics, and the microbiome. J Leukoc Biol 100:881-888
Rosenberg, Helene F (2015) Eosinophil-Derived Neurotoxin (EDN/RNase 2) and the Mouse Eosinophil-Associated RNases (mEars): Expanding Roles in Promoting Host Defense. Int J Mol Sci 16:15442-55
Percopo, Caroline M; Dyer, Kimberly D; Ochkur, Sergei I et al. (2014) Activated mouse eosinophils protect against lethal respiratory virus infection. Blood 123:743-52
Rosenberg, Helene F; Dyer, Kimberly D; Foster, Paul S (2013) Eosinophils: changing perspectives in health and disease. Nat Rev Immunol 13:9-22
Rosenberg, Helene F (2013) Editorial: mouse eosinophils expressing Cre recombinase: endless ""flox""ibilities. J Leukoc Biol 94:3-4
Doyle, Alfred D; Jacobsen, Elizabeth A; Ochkur, Sergei I et al. (2013) Expression of the secondary granule proteins major basic protein 1 (MBP-1) and eosinophil peroxidase (EPX) is required for eosinophilopoiesis in mice. Blood 122:781-90

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