The purpose of the Core is to provide a centralized service to perform experimental histochemical, immunochemical and molecular protocols. The Core will use highly skilled personnel. Liping Huang, a senior technician who has worked with the Core Director for 12 years, has had over 12 years experience in molecular biology, immunohistochemistry, protein chemistry and cell biology. She will provide support for the Core on molecular and protein methodologies. Dr. Mark Stoler (Department of Pathology) is an expert in in situ hybridization. Dr. Alaa Awad is a research associate and has considerable experience in protein and molecular methods. He will provide support in all molecular methods including: RNA isolation, Rnase protection assay, real-time polymerase chain reaction and in situ hybridization. He will interface with project leaders and the Biomedical Research Facility in studies employing DNA microarrays. Susan Ramos, a senior technician with 29 years of expertise in performing immunohistochemistry, transmission- and immunoelectron microscopy experiments, methods will act as a consultant to this Core. The services that the Core will provide include: 1) histochemistry and immunohistochemistry 2) transmission and immunoelectron microscopy, 3) tissue inflammatory cell quantitation, 4) In situ hybridization, 5) RNase protection assay, 6) DNA microarray and 7) quantitative real-time polymerase chain reaction (PCR). We will use a variety of antibodies that have been generated locally or are available commercially or through collaborations. The Core will also take advantage of available resources at the University of Virginia to reduce costs and duplication of services. To accomplish this the Core will interface with: 1)the Reproductive Core Histology Unit to embed tissue sections on a fixed fee schedule and equipment within the University of Virginia Central Electron Microscopy facility equipment and 2) the Biomedical Research Facility to assist with gene chip/microarray studies. The Core will provide the personnel to perform all assays and reagents common to all projects. Project-specific reagents and molecular kits required will be purchased by each project. A centralized service is advantageous for a number of reasons: 1) Generation of consistently high quality results that are comparable between various projects. The results of various assays can be best achieved when performed on a routine basis by skilled personnel. 2) Efficiency of investigators is increased by eliminating tasks that the core facility will undertake. 3) Efficiency is increased and cost is decreased by eliminating duplication of effort and making bulk purchase of supplies.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
1P01HL073361-01A1
Application #
6946743
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2004-08-16
Project End
2009-04-30
Budget Start
2004-08-16
Budget End
2005-04-30
Support Year
1
Fiscal Year
2004
Total Cost
$156,000
Indirect Cost
Name
University of Virginia
Department
Type
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Pei, Hong; Linden, Joel (2016) Adenosine influences myeloid cells to inhibit aeroallergen sensitization. Am J Physiol Lung Cell Mol Physiol 310:L985-92
Cekic, Caglar; Day, Yuan-Ji; Sag, Duygu et al. (2014) Myeloid expression of adenosine A2A receptor suppresses T and NK cell responses in the solid tumor microenvironment. Cancer Res 74:7250-9
Cekic, Caglar; Linden, Joel (2014) Adenosine A2A receptors intrinsically regulate CD8+ T cells in the tumor microenvironment. Cancer Res 74:7239-49
Cekic, Caglar; Sag, Duygu; Day, Yuan-Ji et al. (2013) Extracellular adenosine regulates naive T cell development and peripheral maintenance. J Exp Med 210:2693-706
Barletta, Kathryn E; Cagnina, R Elaine; Wallace, Kori L et al. (2012) Leukocyte compartments in the mouse lung: distinguishing between marginated, interstitial, and alveolar cells in response to injury. J Immunol Methods 375:100-10
Li, Li; Huang, Liping; Ye, Hong et al. (2012) Dendritic cells tolerized with adenosine A?AR agonist attenuate acute kidney injury. J Clin Invest 122:3931-42
Awad, Alaa S; Rouse, Michael D; Khutsishvili, Konstantine et al. (2011) Chronic sphingosine 1-phosphate 1 receptor activation attenuates early-stage diabetic nephropathy independent of lymphocytes. Kidney Int 79:1090-8
Li, Li; Huang, Liping; Vergis, Amy L et al. (2010) IL-17 produced by neutrophils regulates IFN-gamma-mediated neutrophil migration in mouse kidney ischemia-reperfusion injury. J Clin Invest 120:331-42
Reutershan, J; Saprito, M S; Wu, D et al. (2010) Phosphoinositide 3-kinase gamma required for lipopolysaccharide-induced transepithelial neutrophil trafficking in the lung. Eur Respir J 35:1137-47
Sharma, Ashish K; Laubach, Victor E; Ramos, Susan I et al. (2010) Adenosine A2A receptor activation on CD4+ T lymphocytes and neutrophils attenuates lung ischemia-reperfusion injury. J Thorac Cardiovasc Surg 139:474-82

Showing the most recent 10 out of 49 publications