The goal of the Sample Preparation & Storage Core (Core B) is to standardize sample preparation, centralize sample storage and dispersion, and optimize the sharing of resources amongst each project within the P01. Core B services will be directed by the Specific Aims of the four projects that serve as the scientific drivers for this P01. To achieve the overall P01 objectives, Core B will establish an infrastructure that allows for the consistent preparation of samples, organized storage of samples, and the capacity to retrieve stored samples in a functional form. Core B will provide exceptional scientific support with the provision and storage of samples that are collected and prepared using standardization methodology. Core B will be directed by Dr. Daren L. Knoell (PI) and Dr. Patrick Ross Jr. (Co-I) and will be executed through trained clinical and technical support at The Ohio State University (OSU). Dr. Knoell is the Kimberly Professor in the Department of Pharmacy and a member of the Davis Heart and Lung Research Institute with substantial experience in the collection and analysis of human and mouse samples including human peripheral blood mononuclear cells (PBMC), mouse and human bronchoalveloar lavage (BAL) fluid and cells, mouse necropsy for organ harvest, and the culture of phagocytic (monocytes, neutrophils and macrophages) and non- phagocytic (AECI and AECII) cells. Dr. Ross is the chief of Thoracic Surgery and a Professor of Clinical Surgery at OSU Medical Center. Dr. Ross's expertise is in thoracic surgical oncology, robotic surgery, photodynamic therapy, lung volume reduction, and lung transplantation. Dr. Ross and his team have extensive experience in performing bronchoscopies and handling/storing clinical and research specimens and will be responsible for the BAL procedures, including the provision of subject recruitment and consent. Core B will provide centralized support for processing and storage of mouse cells and tissues and centralized support for the scheduling of human subjects for sample donation, consenting of human subjects, and the preparation, dissemination and storage of human samples. Centralized support will be achieved through the following Specific Aims: i) Establish and maintain an infrastructure and operational scheme that supports the management of sample collection, preparation, and storage for each individual project within the P01; and ii) Preparation and dissemination of primary human and mouse cells. Core B will interface with the Administrative Core (Core A) and each individual project through monthly meetings, and through open exchange with regard to the process of preparation, storage, and distribution of cells and fluids.

Public Health Relevance

Samples obtained through the Sample Preparation & Storage Core (Core B) will centralize sample acquisition, standardize sample preparation, and optimize the storage and allocation of resources amongst each project of this Program Project. Core B services are expected to have a positive impact on the Program Project because it is designed to maintain efficient operations with centralized and standardized operating procedures to enhance inter-project coordination while at the same time minimizing to the extent possible, sample numbers.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG051428-02
Application #
9343424
Study Section
Special Emphasis Panel (ZAG1-ZIJ-8)
Program Officer
Fuldner, Rebecca A
Project Start
Project End
2017-09-02
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
2
Fiscal Year
2017
Total Cost
$108,397
Indirect Cost
$38,125
Name
Ohio State University
Department
Type
Domestic Higher Education
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Piergallini, Tucker J; Turner, Joanne (2018) Tuberculosis in the elderly: Why inflammation matters. Exp Gerontol 105:32-39
Moliva, J I; Hossfeld, A P; Canan, C H et al. (2018) Exposure to human alveolar lining fluid enhances Mycobacterium bovis BCG vaccine efficacy against Mycobacterium tuberculosis infection in a CD8+ T-cell-dependent manner. Mucosal Immunol 11:968-978
Ault, Russell; Dwivedi, Varun; Koivisto, Elisha et al. (2018) Altered monocyte phenotypes but not impaired peripheral T cell immunity may explain susceptibility of the elderly to develop tuberculosis. Exp Gerontol 111:35-44
Seveau, Stephanie; Turner, Joanne; Gavrilin, Mikhail A et al. (2018) Checks and Balances between Autophagy and Inflammasomes during Infection. J Mol Biol 430:174-192
Kenney, Adam D; Dowdle, James A; Bozzacco, Leonia et al. (2017) Human Genetic Determinants of Viral Diseases. Annu Rev Genet 51:241-263
Scordo, Julia M; Arcos, Jesús; Kelley, Holden V et al. (2017) Mycobacterium tuberculosis Cell Wall Fragments Released upon Bacterial Contact with the Human Lung Mucosa Alter the Neutrophil Response to Infection. Front Immunol 8:307
Torrelles, Jordi B; Schlesinger, Larry S (2017) Integrating Lung Physiology, Immunology, and Tuberculosis. Trends Microbiol 25:688-697
Moliva, Juan I; Turner, Joanne; Torrelles, Jordi B (2017) Immune Responses to Bacillus Calmette-Guérin Vaccination: Why Do They Fail to Protect against Mycobacterium tuberculosis? Front Immunol 8:407