The Morphology Core will provide technical expertise, assistance and equipment to those investigators who wish to analyze their experiments using microscopic and morphometric techniques. Expertise and assistance will be provided by core personnel in the following areas: (1) routine light microscopy and histochemical analysis, (2) enzyme histochemistry, (3) immunohistochemistry, (4) in situ hybridization histochemistry, (5) autoradiography, (6) photomicroscopy, (7) electron microscopy, (8) confocal microscopy, (9) computer-assisted image analysis, and (10) morphometry. In addition, the Morphology Core will facilitate the acquisition, processing and storage of experimental and control tissues; maintain standards and quality control for histochemical procedures; and assist in the development of new techniques as needed. The Morphology Core will also be responsible for immunohistochemical and in situ hybridization analyses of human biopsy and autopsy material related to neonatal respiratory distress syndrome pulmonary alveolar proteinosis, hyaline membrane disease, bronchopulmonary dysplasia, interstitial lung disease, emphysema, and pulmonary malformations. The overall goal of these clinical studies will be to characterize and identify mechanisms that cause idiopathic lung disease and developmental abnormalities.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
2P50HL056387-06
Application #
6500797
Study Section
Project Start
1996-09-01
Project End
2006-07-31
Budget Start
Budget End
Support Year
6
Fiscal Year
2001
Total Cost
$219,976
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Hahn, Andrew D; Higano, Nara S; Walkup, Laura L et al. (2017) Pulmonary MRI of neonates in the intensive care unit using 3D ultrashort echo time and a small footprint MRI system. J Magn Reson Imaging 45:463-471
Korsten, Peter; Strohmayer, Katharina; Baughman, Robert P et al. (2016) Refractory pulmonary sarcoidosis - proposal of a definition and recommendations for the diagnostic and therapeutic approach. Clin Pulm Med 23:67-75
Lammi, Matthew R; Baughman, Robert P; Birring, Surinder S et al. (2015) Outcome Measures for Clinical Trials in Interstitial Lung Diseases. Curr Respir Med Rev 11:163-174
Perl, Anne-Karina T; Gale, Emily (2009) FGF signaling is required for myofibroblast differentiation during alveolar regeneration. Am J Physiol Lung Cell Mol Physiol 297:L299-308
Wert, Susan E; Whitsett, Jeffrey A; Nogee, Lawrence M (2009) Genetic disorders of surfactant dysfunction. Pediatr Dev Pathol 12:253-74
Bridges, James P; Xu, Yan; Na, Cheng-Lun et al. (2006) Adaptation and increased susceptibility to infection associated with constitutive expression of misfolded SP-C. J Cell Biol 172:395-407
Bullard, Janine E; Wert, Susan E; Whitsett, Jeffrey A et al. (2005) ABCA3 mutations associated with pediatric interstitial lung disease. Am J Respir Crit Care Med 172:1026-31
Shannon, John M; Hyatt, Brian A (2004) Epithelial-mesenchymal interactions in the developing lung. Annu Rev Physiol 66:625-45
Akeson, A L; Brooks, S K; Thompson, F Y et al. (2001) In vitro model for developmental progression from vasculogenesis to angiogenesis with a murine endothelial precursor cell line, MFLM-4. Microvasc Res 61:75-86
Akeson, A L; Wetzel, B; Thompson, F Y et al. (2000) Embryonic vasculogenesis by endothelial precursor cells derived from lung mesenchyme. Dev Dyn 217:23-Nov