The Cell Imaging and Analysis Core is designed to provide state-of-the- art and quality-assured morphologically oriented services to the four individual projects within the program. Fundamental to the successful delivery of such services is the ongoing research interests of the core leader, who is independently committed to elucidation of the pathology of lung disease and reparative mechanisms. The detection of specific protein constituents and products of cells by biochemical and immunohistochemical methods provides a critical foundation for elucidating the role of protein production in health and disease. Together, the results of the studies to be implemented will provide critical information defining the importance of subpopulations of cells responding to specific conditions. With the advent of immunocytochemical, in situ hybridization, and green fluorescent protein-tagged molecule studies, methods for assessing reaction products in tissues and cells have become increasingly important. However, traditional morphologic assessment has evolved to more quantitative and less subjective techniques. The Cell Imaging and Analysis Core has sophisticated state-of-the-art microscopic equipment that can provide digital images that can be subsequently processed and analyzed by available computer-based methods. Thus, the Cell Imaging and Analysis Core will provide centralized facilities and techniques designed to be used in collaboration with project investigators in the pursuit of the specific aims of individual projects.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
1P01HL067004-01
Application #
6452917
Study Section
Heart, Lung, and Blood Program Project Review Committee (HLBP)
Project Start
2001-06-01
Project End
2006-04-30
Budget Start
Budget End
Support Year
1
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Vermont & St Agric College
Department
Type
DUNS #
066811191
City
Burlington
State
VT
Country
United States
Zip Code
05405
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Sabo-Attwood, Tara; Ramos-Nino, Maria E; Eugenia-Ariza, Maria et al. (2011) Osteopontin modulates inflammation, mucin production, and gene expression signatures after inhalation of asbestos in a murine model of fibrosis. Am J Pathol 178:1975-85
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Manning, Christopher B; Sabo-Attwood, Tara; Robledo, Raymond F et al. (2008) Targeting the MEK1 cascade in lung epithelium inhibits proliferation and fibrogenesis by asbestos. Am J Respir Cell Mol Biol 38:618-26
Barlow, Christy A; Kitiphongspattana, Kajorn; Siddiqui, Nazli et al. (2008) Protein kinase A-mediated CREB phosphorylation is an oxidant-induced survival pathway in alveolar type II cells. Apoptosis 13:681-92
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Mossman, Brooke T (2008) Assessment of the pathogenic potential of asbestiform vs. nonasbestiform particulates (cleavage fragments) in in vitro (cell or organ culture) models and bioassays. Regul Toxicol Pharmacol 52:S200-3
Levis, Jamie; Loi, Roberto; Butnor, Kelly J et al. (2008) Decreased asbestos-induced lung inflammation and fibrosis after radiation and bone marrow transplant. Am J Respir Cell Mol Biol 38:16-25
Dostert, Catherine; Petrilli, Virginie; Van Bruggen, Robin et al. (2008) Innate immune activation through Nalp3 inflammasome sensing of asbestos and silica. Science 320:674-7

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