The mouse asthma model core (scientific core C) will coordinate and perform the experiments in projects2, 3 and 4 that involve the mouse asthma model. In Project 4, the Leader, Dr. Spiegel, has developedspecific inhibitors for sphingosine-1-kinase and will use these in an inhalent model to get them directly tothe lung. This largely avoids systemic toxicity and targets the affected organ directly. The concept beingtested is whether inhibition of lung mast cells is sufficient to inhibit the asthma model. In addition, theprogram director will use siRNA to block, in vivo, in lung the synthesis of sphingosine kinase in order todetermine whether this will inhibit asthma development. In Project 2, Dr. Conrad has demonstrated thatoverexperssion of CD23 inhibits IgE production and eosinophil recruitment to the lung. Experiments willbe performed to determine if IgE is necessary for the eosinophil recruitment. In addition, the CD23sheddase has been identified as ADAM 10 and siRNA knock-down experiments will be performed incollaboration with Dr. Spiegel to determine if blockade of ADAM10 in the lung, either by siRNA or specificinhibitors influences asthma development and symptoms. In Project #3, Dr. Ryan is examining theallergic phenotype of lyn knockout animals with the objective of determining the activities of lyn in themast cell. The lyn''' mice are known to develop severe Th2 disease including increased IgE andeosinophil responses. These activities, not surprisingly, lead to a severe asthma phenotype. Incollaboration with Dr, Conrad, the lyn''' animals will be crossed to CD23 transgenics to see if the Th2disease is modulated. In addition, the activities of ADAM10 inhibitors either via a siRNA or chemicalinhibitor methodology, introduced directly into the lung, will be tested for capacity to modulate the lyn'''severe Th2 disease modality. In all of these studies, the core will provide the expertise to both performand analyze data from the mouse asthma model. These include maintenance of mice for the 30 dayperiod required for sensitization, aerosol challenge and ultimate sacrifice with BAL fluid collection andlung preparation for histology and RNA analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI077435-01
Application #
7476207
Study Section
Special Emphasis Panel (ZAI1-QV-I (J1))
Project Start
2008-04-01
Project End
2013-03-31
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
1
Fiscal Year
2008
Total Cost
$185,852
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
DUNS #
105300446
City
Richmond
State
VA
Country
United States
Zip Code
23298
Oyeniran, Clement; Sturgill, Jamie L; Hait, Nitai C et al. (2015) Aberrant ORM (yeast)-like protein isoform 3 (ORMDL3) expression dysregulates ceramide homeostasis in cells and ceramide exacerbates allergic asthma in mice. J Allergy Clin Immunol 136:1035-46.e6
Oskeritzian, Carole A; Hait, Nitai C; Wedman, Piper et al. (2015) The sphingosine-1-phosphate/sphingosine-1-phosphate receptor 2 axis regulates early airway T-cell infiltration in murine mast cell-dependent acute allergic responses. J Allergy Clin Immunol 135:1008-18.e1
Kim, Eugene Y; Sturgill, Jamie L; Hait, Nitai C et al. (2014) Role of sphingosine kinase 1 and sphingosine-1-phosphate in CD40 signaling and IgE class switching. FASEB J 28:4347-58
Faber, Travis W; Pullen, Nicholas A; Fernando, Josephine F A et al. (2014) ADAM10 is required for SCF-induced mast cell migration. Cell Immunol 290:80-8
Le, Quang Trong; Lotfi-Emran, Sahar; Min, Hae-Ki et al. (2014) A simple, sensitive and safe method to determine the human ?/?-tryptase genotype. PLoS One 9:e114944
Lyons, Jonathan J; Sun, Guangping; Stone, Kelly D et al. (2014) Mendelian inheritance of elevated serum tryptase associated with atopy and connective tissue abnormalities. J Allergy Clin Immunol 133:1471-4
Martin, Rebecca K; Saleem, Sheinei J; Folgosa, Lauren et al. (2014) Mast cell histamine promotes the immunoregulatory activity of myeloid-derived suppressor cells. J Leukoc Biol 96:151-9
Morales, Johanna K; Saleem, Sheinei J; Martin, Rebecca K et al. (2014) Myeloid-derived suppressor cells enhance IgE-mediated mast cell responses. J Leukoc Biol 95:643-50
Liang, Jie; Nagahashi, Masayuki; Kim, Eugene Y et al. (2013) Sphingosine-1-phosphate links persistent STAT3 activation, chronic intestinal inflammation, and development of colitis-associated cancer. Cancer Cell 23:107-20
Nagahashi, Masayuki; Kim, Eugene Y; Yamada, Akimitsu et al. (2013) Spns2, a transporter of phosphorylated sphingoid bases, regulates their blood and lymph levels, and the lymphatic network. FASEB J 27:1001-11

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