Cytokines are important modulators of the immune response that underlies the inflammatory process in atopic forms of asthma. IL-4 and IL-13 are important cytokines for the regulation of these asthmatic immune responses. Work over the past ten years has identified many signaling molecules activated by these cytokines and outlined the basic mechanisms by which binding of these cytokines to their receptor leads to this activation. What remains unknown is how these signaling events are integrated by the cell into a biologic response. We have begun to address this question by using Affymetrix oligonucleotide arrays to define how different signaling pathways activated by these cytokines regulate gene transcription. This work has identified novel genes induced by IL-4. We propose to determine if the proteins encoded for by these genes are important for IL-4 function. In addition, we will extend our work with microarrays to determine how activation of different signaling molecules by IL-4 converges in a coordinated regulation of gene expression. Finally, recent data suggest that polymorphisms in the genes encoding some of these signaling molecules are associated with either asthma or atopy. We will determine if these allelic variants lead to alteration in IL-4 induced gene expression. Together, these results will provide investigators in asthma research important information regarding the function of these cytokines. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
7R01AI054821-03
Application #
7084202
Study Section
Immunological Sciences Study Section (IMS)
Program Officer
Plaut, Marshall
Project Start
2003-04-15
Project End
2008-03-31
Budget Start
2005-01-01
Budget End
2005-03-31
Support Year
3
Fiscal Year
2004
Total Cost
$233,181
Indirect Cost
Name
University of Iowa
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Gorman, Jacob V; Colgan, John D (2018) Acute stimulation generates Tim-3-expressing T helper type 1 CD4 T cells that persist in vivo and show enhanced effector function. Immunology 154:418-433
Barr, Jennifer Y; Goodfellow, Renee X; Colgan, Diana F et al. (2017) Early B Cell Progenitors Deficient for GON4L Fail To Differentiate Due to a Block in Mitotic Cell Division. J Immunol 198:3978-3988
Phong, Binh L; Avery, Lyndsay; Sumpter, Tina L et al. (2015) Tim-3 enhances Fc?RI-proximal signaling to modulate mast cell activation. J Exp Med 212:2289-304
Gorman, Jacob V; Colgan, John D (2014) Regulation of T cell responses by the receptor molecule Tim-3. Immunol Res 59:56-65
Gorman, Jacob V; Starbeck-Miller, Gabriel; Pham, Nhat-Long L et al. (2014) Tim-3 directly enhances CD8 T cell responses to acute Listeria monocytogenes infection. J Immunol 192:3133-42
Duong, Khanh L; Das, Satyabrata; Yu, Shuyang et al. (2014) Identification of hematopoietic-specific regulatory elements from the CD45 gene and use for lentiviral tracking of transplanted cells. Exp Hematol 42:761-72.e1-10
Gorman, Jacob V; Colgan, John D (2014) Response to Comment on ""Tim-3 directly enhances CD8 T cell responses to acute Listeria monocytogenes infection"". J Immunol 193:467-8
Sharma, S; Sheehy, T; Kolonel, L N (2013) Contribution of meat to vitamin B??, iron and zinc intakes in five ethnic groups in the USA: implications for developing food-based dietary guidelines. J Hum Nutr Diet 26:156-68
Curtiss, Miranda L; Gorman, Jacob V; Businga, Thomas R et al. (2012) Tim-1 regulates Th2 responses in an airway hypersensitivity model. Eur J Immunol 42:651-61
Hostager, Bruce S; Kashiwada, Masaki; Colgan, John D et al. (2011) HOIL-1L interacting protein (HOIP) is essential for CD40 signaling. PLoS One 6:e23061

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