Our long-term goal is to understand how eosinophils (EOS) traffic to and interact in the ainway and contribute to the progression of asthma. aM32 integrin (CD11b/CD18) is highly activated on EOS obtained by bronchoalveolar lavage after segmental antigen challenge, suggesting that aM(32 functions becomes important as EOS extravasate to and migrate in the lung. However, little is known about roles of aMp2 and relevant ligand(s) in adhesion, migration, and activities of EOS in the airway. The overall objective of this proposal is to determine the role of aMp2 in modulating behavior of EOS in the ainway. Based on our preliminary data and current understanding of EOS biology and the extracellular matrix (ECM) in asthma, the current hypothesis is that periostin, an ECM protein characteristic of inflammation driven by T helper type 2 cells and found in the asthmatic ain/vay, is a dominant adhesive ligand for EOS aMp2 integrin and that the aMp2-periostin interaction is an important determinant of EOS function.
Aim 1 is to define roles of aMp2, periostin and TGF-P-induced protein (TGFBI), a periostin homolog also found in lung, in adhesion, migration, sun/ival, and other functions of EOS activated by IL-3, IL-5, GM-CSF, or other activators.
Aim 2 is to determine the structure-function relationship ofthe recognition of periostin by aMP2, map the aMp2-binding site(s), and define minimal constructs that when immobilized support, and when soluble block, EOS adhesion and migration. How the vitamin K-dependent y-carboxylation and alternative splicing affect periostin's biological activities will also be determined.
Aim 3 is to understand the mechanism and significance ofthe striking increase of periostin that is found in the asthmatic airway. Periostin secretion from fibroblasts and epithelial cells stimulated by TGF-p or other factors, as well as its deposition into ECM and turnover will be analyzed. Antibodies to the various forms of periostin and TGFBI will be developed for localization in bronchial biopsies after segmental antigen challenge. Achieving the goals of this proposal will provide novel knowledge and a better understanding of EOS trafficking and functions and the interplay between EOS and the ECM in Th2-driven inflammation, and will generate agents and reagents that will allow this interplay to be studied and modulated. RELE^VANCE (See instructions): The proposed research will determine how the connective tissue protein periostin, which is strongly up- regulated in asthma, interacts with its cell-surface receptor protein aMP2 integrin (CD11b/CD18) on activated EOS, and supports attachment and migration of EOS. The project will provide new insights into the movement of EOS in the asthmatic ainway and the biology of connective tissue in the diseased lung.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL088594-07
Application #
8646955
Study Section
Heart, Lung, and Blood Program Project Review Committee (HLBP)
Project Start
Project End
Budget Start
2014-04-01
Budget End
2015-03-31
Support Year
7
Fiscal Year
2014
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
City
Madison
State
WI
Country
United States
Zip Code
Tomasini-Johansson, Bianca R; Mosher, Deane F (2018) Microtiter assays for quantitation of assembly of plasma and cellular fibronectin. Methods Cell Biol 143:157-170
Turton, Keren B; Wilkerson, Emily M; Hebert, Alex S et al. (2018) Expression of novel ""LOCGEF"" isoforms of ARHGEF18 in eosinophils. J Leukoc Biol 104:135-145
Bernau, Ksenija; Leet, Jonathan P; Esnault, Stephane et al. (2018) Eosinophil-degranulation products drive a proinflammatory fibroblast phenotype. J Allergy Clin Immunol 142:1360-1363.e3
Stallings, Nancy R; O'Neal, Melissa A; Hu, Jie et al. (2018) Pin1 mediates A?42-induced dendritic spine loss. Sci Signal 11:
Moon, Hyung-Geun; Kim, Seung-Jae; Jeong, Jong Jin et al. (2018) Airway Epithelial Cell-Derived Colony Stimulating Factor-1 Promotes Allergen Sensitization. Immunity 49:275-287.e5
Khoury, Paneez; Akuthota, Praveen; Ackerman, Steven J et al. (2018) Revisiting the NIH Taskforce on the Research needs of Eosinophil-Associated Diseases (RE-TREAD). J Leukoc Biol 104:69-83
Johansson, Mats W; Kelly, Elizabeth A; Nguyen, Christopher L et al. (2018) Characterization of Siglec-8 Expression on Lavage Cells after Segmental Lung Allergen Challenge. Int Arch Allergy Immunol 177:16-28
Evans, Michael D; Esnault, Stephane; Denlinger, Loren C et al. (2018) Sputum cell IL-1 receptor expression level is a marker of airway neutrophilia and airflow obstruction in asthmatic patients. J Allergy Clin Immunol 142:415-423
Esnault, Stephane; Hebert, Alexander S; Jarjour, Nizar N et al. (2018) Proteomic and Phosphoproteomic Changes Induced by Prolonged Activation of Human Eosinophils with IL-3. J Proteome Res 17:2102-2111
Bortnov, Valeriu; Annis, Douglas S; Fogerty, Frances J et al. (2018) Myeloid-derived growth factor is a resident endoplasmic reticulum protein. J Biol Chem 293:13166-13175

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