Mesenchymal stem or stromal cells (MSCs) are adult connective tissue progenitor cells with multilineage differentiation and anti-inflammatory properties. Due to these properties, MSCs are being evaluated as cellular therapy for regenerative medicine and inflammatory diseases. This proposal will address two critical issues related with MSCs biology;i) to understand the mechanisms of mesenchymal stem/stromal cell-mediated attenuation of acute lung injury in a relevant large animal model and ii) to examine if MSCs therapy influences the host immune response to influenza virus infection. Several studies in mouse models have suggested that MSCs attenuate lung injury and enhance lung repair. Most of the data of evaluation of MSCs as cellular therapy for human diseases have come from rodent models. However, the mechanisms of immunoregulation by mouse MSCs are different than those of human MSCs. Therefore, there is a need to conduct studies in clinically relevant animal model that closely resembles to humans in anatomy, physiology, body size and host response. In this application, we will use well defined LPS induced lung injury in pig as a model of human acute lung injury (ALI) to examine the mechanisms of MSC-mediated attenuation of ALI. First, we will isolate MSCs from bronchoalveolar lavage fluid (BAL) and bone marrow (BM). We will examine cell proliferation, colony formation, in vitro differentiation potential and their immunomodulatory properties. Next, we will examine mechanisms by which multipotent BAL/BM-MSCs attenuate acute lung injury and facilitate lung repair. We will exogenously administer in vitro expanded MSCs 24 hours after the onset of LPS-induced lung injury. We will examine the number of MSCs engrafting to the injured lung;effect on endogenous epithelial cell differentiation/proliferation;effect on macrophages, dendritic cells, T cells and NK cells functios and their effect on the attenuation of the disease and tissue repair and regeneration. In second objective, we will examine the effect of MSC-mediated immunoregulation in ALI in pig on anti-influenza immunity and virus clearance in pig model. Two, 4 and 6-weeks after MSCs therapy for ALI, we will infect pigs influenza virus. We will examine virus shedding, virus titers in lungs cytokines, chemokines, histological lung lesions, and virus- specific proliferating CD4 and CD8 T cells. The findings of these studies will provide new insights into the mechanisms of MSC-mediated beneficial effects in a relevant large animal model. Also, data obtained from this proposal will help to design preventive measures for the control of influenza virus infections in stem cell transplant patients.

Public Health Relevance

Mesenchymal stem/stromal cells (MSCs) possess anti-inflammatory and tissue repair properties and are being evaluated as cellular therapy for several auto-immune and inflammatory diseases including acute lung injury (ALI). However, mechanisms by which MSCs mediate these beneficial effects are not completely understood. Most of the data on attenuation of ALI by MSCs come from mouse models. Due to significant differences in body size, anatomy, physiology and immunology between mice and humans, results obtained from mouse models are not always reproduced in human clinical trials. In this application, we will examine the mechanisms of anti-inflammatory and tissue repair potential of porcine bone marrow and bronchoalveolar fluid in a pig model of acute lung injury ALI. Pigs are very close to humans in terms of anatomy, physiology, body size and immune responses;therefore, finding of these studies will provide valuable insights for designing new clinical interventions for the better management of ALI in humans. Secondly, we will examine if MSCs mediated immunomodulation of immune cells in ALI model has any adverse effect on anti-influenza virus immunity in pigs.

Agency
National Institute of Health (NIH)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21HL125191-01
Application #
8772394
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Harabin, Andrea L
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Ohio State University
Department
Zoology
Type
Earth Sciences/Resources
DUNS #
City
Columbus
State
OH
Country
United States
Zip Code
43210