Effector cell lineage commitment in allergic inflammation Project summary: The recruitment and expansion of progenitor cells to the lung may be critical for the maintenance and propagation of chronic airway inflammation in asthma. The origin of the tissue mast cell progenitor remains elusive. The current paradigm describing the origin of the mast cell states that mast cells are derived from hematopoietic (CD45+) bone marrow progenitors, travel though the circulation, and complete their differentiation in diverse target tissues. Preliminary data included in this proposal suggest that 1. a non-hematopoietic progenitor cell (CD45-), previously implicated as a vascular progenitor in vivo, can differentiate into a mast cell, and 2. development of mast cells from CD45- progenitors is increased in asthmatic subjects. This proposal hypothesizes that the mast cell can be derived from a non-hematopoietic, multipotent progenitor whose ultimate lineage commitment is directed by disease-specific microenvironmental factors in asthma. Experiments in Aim 1 seek to define the determinants of CD45- non-hematopoietic progenitor cell differentiation into mast cells. Experiments in this aim propose to identify the cytokine signaling pathways critical for mast cell lineage commitment, test the hypothesis that activation of STAT5 is necessary for mast cell differentiation, and explore mast cell transcriptional networks with emphasis on direct programming of progenitors to mast cells. Experiments propose to test the hypothesis that Th2 cytokines such as IL-4 directly contribute to the multipotent potential of these progenitors by modulating multipotency, self-renewal, and chromatin remodeling genes. Experiments in Aim 2 propose to address the role of mast cells derived from CD45- progenitor cells in human asthma by identifying these progenitors in the peripheral blood of asthmatic vs. normal subjects and identifying CD45- mast cells in human lung pathology specimens, including in those with gender-mismatched lung transplants. The unique functional properties of CD45- mast cells will be studied in organotypic co-culture with human airway epithelial cells derived from normal and asthmatic donors. If successful, these studies will have identified a novel, nonhematopoietic mast cell progenitor, clarified the mechanisms by which these progenitors commit to mast cell development, implicated Th2 cytokines in influencing multipotency gene expression, articulated the role of these cells in human asthma, and proposed new targets for asthma therapeutics.

Public Health Relevance

Mast cells play an important role in airway inflammation in asthma but the origin of the tissue mast cell remains poorly understood. This project investigates the role of a novel mast cell progenitor and seeks to define the mechanisms controlling mast cell development in asthma. Understanding mast cell development in asthma may help develop to novel treatments targeting mast cells in asthma.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56HL119321-01A1
Application #
9130428
Study Section
Lung Cellular, Molecular, and Immunobiology Study Section (LCMI)
Program Officer
Noel, Patricia
Project Start
2015-09-01
Project End
2016-08-31
Budget Start
2015-09-01
Budget End
2016-08-31
Support Year
1
Fiscal Year
2015
Total Cost
$396,250
Indirect Cost
$146,250
Name
Cleveland Clinic Lerner
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
135781701
City
Cleveland
State
OH
Country
United States
Zip Code
44195
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Banga, Amit; Han, Yingchun; Wang, Xiaofeng et al. (2016) Mast cell phenotypes in the allograft after lung transplantation. Clin Transplant 30:845-51