The Histology & Imaging Core will serve Gene Therapy PPG investigators associated with each individual project by offering a broad spectrum of services related to quantitative biological imaging of whole animals, tissues and cell cultures of interest. The Core has supported the UNC Gene Therapy for CF projects since 1993 and has increased its output and capabilities to meet growing research demands. For example, many specimens will be processed for standard, paraffin- or plastic-based histology, with sections stained with hematoxylin and eosin for general survey purposes, and unstained sections provided to the submitting investigator for immuno- or other special purpose staining. Core personnel will also be responsible for histological staining procedures, associated light or electron microscopy, and imaging. Alternately, human cell cultures will be submitted for direct staining procedures and imaging by widefield or confocal light microscopy. Mice, injected or exposed to viral vectors carrying fluorescent (e.g. GFP, RFP) or luminescent (e.g. luciferase) markers will be submitted to the Histology & Imaging Core for whole body imaging with ultra sensitive, cryo-cooled digital cameras. The Histology & Imaging Core is comprised of three laboratories specializing in histology (including electron microscopy), light microscopy, and whole animal imaging. Each of these laboratories is equipped with state-of-the-art instrumentation including Leica tissue processing equipment and microtomes, Leica and Zeiss laser scanning confocal (3) and Perkin-Elmer spinning disc (1) microscopes. Lastly, the laboratories are staffed by highly skilled, highly productive personnel decicated to the success of the projects. The H & I core will facilitate all projects by providing services that are unique and specific to the study of gene delivery to airway cells. Through these functions, and in conjunction with other Cores in this application, the Histology & Imaging Core will support research towards the development of safe and effective gene therapy for CF.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL051818-13
Application #
7252019
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
13
Fiscal Year
2006
Total Cost
$133,162
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Goudy, Kevin S; Johnson, Mark C; Garland, Alaina et al. (2011) Inducible adeno-associated virus-mediated IL-2 gene therapy prevents autoimmune diabetes. J Immunol 186:3779-86
Li, Wuping; Zhang, Liqun; Wu, Zhijian et al. (2011) AAV-6 mediated efficient transduction of mouse lower airways. Virology 417:327-33
Zhang, Liqun; Collins, Peter L; Lamb, Robert A et al. (2011) Comparison of differing cytopathic effects in human airway epithelium of parainfluenza virus 5 (W3A), parainfluenza virus type 3, and respiratory syncytial virus. Virology 421:67-77
Johnson, Jarrod S; Gentzsch, Martina; Zhang, Liqun et al. (2011) AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosis. PLoS Pathog 7:e1002053
Johnson, Jarrod S; Li, Chengwen; DiPrimio, Nina et al. (2010) Mutagenesis of adeno-associated virus type 2 capsid protein VP1 uncovers new roles for basic amino acids in trafficking and cell-specific transduction. J Virol 84:8888-902
Kwilas, Anna R; Yednak, Mark A; Zhang, Liqun et al. (2010) Respiratory syncytial virus engineered to express the cystic fibrosis transmembrane conductance regulator corrects the bioelectric phenotype of human cystic fibrosis airway epithelium in vitro. J Virol 84:7770-81
Mitchell, Angela M; Nicolson, Sarah C; Warischalk, Jayme K et al. (2010) AAV's anatomy: roadmap for optimizing vectors for translational success. Curr Gene Ther 10:319-340
Zhang, Liqun; Limberis, Maria P; Thompson, Catherine et al. (2010) ?-Fetoprotein gene delivery to the nasal epithelium of nonhuman primates by human parainfluenza viral vectors. Hum Gene Ther 21:1657-64
Li, C; Hirsch, M; Carter, P et al. (2009) A small regulatory element from chromosome 19 enhances liver-specific gene expression. Gene Ther 16:43-51
Limberis, Maria P; Vandenberghe, Luk H; Zhang, Liqun et al. (2009) Transduction efficiencies of novel AAV vectors in mouse airway epithelium in vivo and human ciliated airway epithelium in vitro. Mol Ther 17:294-301

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