The Cell Culture and Translational Studies Core, designated as Core B, is a centralized facility that provides primary alveolar epithelial type 2 and type 1 cells and macrophages from humans, rats, and mice, as well as rat and mouse fibroblasts, to each of the three projects and to Core C. Core B also maintains secondary lung cell lines for the PPG. Centralization of the cell culture facilities will ensure that a continuous supply of high- quality alveolar epithelial and macrophage cells are available to each of the three projects. The Core personnel has extensive experience in the isolation of primary alveolar type 2 and type 1 cells and macrophages from human, rat, and mouse lungs, as well as general cell culture techniques. The consolidated cell culture facility provides an economical means of isolating and culturing primary and secondary cells. This translates into reduced overall costs (i.e., personnel, reagents, and animals) and more importantly maintains the quality of the cells used in research. Additionally, Core B will facilitate translational research by coordinating the collection, analysis, and generation of a database of biological samples from ARDS patients and distributing BALF samples to the project investigators to be used according to the research plan outlined in Projects 1, 2, and 3.
Currently, there are no established cell lines that maintain the phenotype characteristics of primary alveolar epithelial cells. Consequently, it is necessary to isolate the alveolar epithelial cells from human and rodent lung specimens. Also, the investigators of each of the three projects require the isolation of primary cells of both epithelial and macrophages from genetically modified mice. To facilitate translational research, Core B will coordinate the collection and analysis of biological samples from ARDS patients. Biological samples will be made available to the project investigators to be used according to the research plans outlined in Projects 1, 2, and 3.
| Sala, Marc A; Balderas-Martínez, Yalbi Itzel; Buendía-Roldan, Ivette et al. (2018) Inflammatory pathways are upregulated in the nasal epithelium in patients with idiopathic pulmonary fibrosis. Respir Res 19:233 |
| Mehta, Manan M; Weinberg, Samuel E; Steinert, Elizabeth M et al. (2018) Hexokinase 2 is dispensable for T cell-dependent immunity. Cancer Metab 6:10 |
| Brazee, Patricia L; Dada, Laura A (2018) Splice Wars: The Role of MLCK Isoforms in Ventilation-induced Lung Injury. Am J Respir Cell Mol Biol 58:549-550 |
| Koch, Clarissa M; Chiu, Stephen F; Akbarpour, Mahzad et al. (2018) A Beginner's Guide to Analysis of RNA Sequencing Data. Am J Respir Cell Mol Biol 59:145-157 |
| Dela Cruz, Charles S; Wunderink, Richard G; Christiani, David C et al. (2018) Future Research Directions in Pneumonia. NHLBI Working Group Report. Am J Respir Crit Care Med 198:256-263 |
| Kong, Hyewon; Chandel, Navdeep S (2018) Regulation of redox balance in cancer and T cells. J Biol Chem 293:7499-7507 |
| Hsiao, Hsi-Min; Fernandez, Ramiro; Tanaka, Satona et al. (2018) Spleen-derived classical monocytes mediate lung ischemia-reperfusion injury through IL-1?. J Clin Invest 128:2833-2847 |
| Wang, Zheng; Divanyan, Alex; Jourd'heuil, Frances L et al. (2018) Vimentin expression is required for the development of EMT-related renal fibrosis following unilateral ureteral obstruction in mice. Am J Physiol Renal Physiol 315:F769-F780 |
| Lu, Ziyan; Casalino-Matsuda, S Marina; Nair, Aisha et al. (2018) A role for heat shock factor 1 in hypercapnia-induced inhibition of inflammatory cytokine expression. FASEB J 32:3614-3622 |
| Amarelle, Luciano; Lecuona, Emilia (2018) A Nonhospitable Host: Targeting Cellular Factors as an Antiviral Strategy for Respiratory Viruses. Am J Respir Cell Mol Biol 59:666-667 |
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