The Flow Cytometry and Cell Sorting Core is an established core for the VDDRC. It has been supported on member requests and approved by the Executive Committee and the Scientific Advisory Board with substantial institutional support provided by the university. This core provides access to state-of-the-art equipment for analytical cytometric analysis, ceil counts and viability, and cell sorting, and it provides expert training and consulting on the use of these methodologies. The core facility maintains three LSRII analytical cytometers, a new Fortessa analytical machine, two FACSAria cell sorters, a Guava sheathless cytometer and associated data processing and software workstations. We offer paramagnetic pre-sorting with a Miltenyi AutoMACS. The core provides both Mac and PC workstations, an extensive toolbox of software for flow cytometry, and digital backup of data on a remote server. The core also houses facilities for immunologic assays using automated ELISpot readers, as well as access to a plate-loading cytometer for cytokine bead arrays or multiplex assays for other soluble factors. The staff provides both group and one-on one instruction to facilitate development of acquisition and analysis skills for all users. Trained users can use the analytical cytometers directly;sorting is an assisted-only service. The core also has worked with several of the VDDRC investigators to develop novel sorting techniques for elements of subcellular compartments such as vesicles. This technically forward work requires custom modification of the sorting cytometer in collaboration with the manufacturer, and involves a large number of technical components from gradient preparations, staining, lasers and fluidics, and downstream collection and proteomics analysis. This innovative work using polarized epithelial cells could not be conducted by individual investigators apart from the development team we have created. The core maintains an active development program to keep the instrumentation and systems current, functional, accessible, and easy to use. In fact, a number of our machines have been extensively customized with four or five lasers and special PMTs to accommodate user protocols. Individual researchers could not support this type of high-quality cytometry in their own labs due to the high cost of the instrumentation and maintenance. This core improves human health through the provision of technologies that increase prevention, diagnosis or treatment of digestive disease disorders.
The Flow Cytometry Core Laboratory provides state-of-the-art high-end cytometry equipment and expert cytometrists to help DDRC investigators perform experiments to analyze cell populations in a highly quantitative way. The Core allows investigators to measure cell of particular types and also to physically sort and recover cells of interest for further study. This level of custom equipment and expertise otherwise would not be available to investigators.
|Hong, Jun; Chen, Zheng; Peng, Dunfa et al. (2016) APE1-mediated DNA damage repair provides survival advantage for esophageal adenocarcinoma cells in response to acidic bile salts. Oncotarget 7:16688-702|
|Hurlow, J; Blanz, E; Gaddy, J A (2016) Clinical investigation of biofilm in non-healing wounds by high resolution microscopy techniques. J Wound Care 25 Suppl 9:S11-22|
|Banks, Leah D; Amoah, Priscilla; Niaz, Mohammad S et al. (2016) Olive oil prevents benzo(a)pyrene [B(a)P]-induced colon carcinogenesis through altered B(a)P metabolism and decreased oxidative damage in Apc(Min) mouse model. J Nutr Biochem 28:37-50|
|Taverna, Domenico; Pollins, Alonda C; Nanney, Lillian B et al. (2016) Histology-guided protein digestion/extraction from formalin-fixed and paraffin-embedded pressure ulcer biopsies. Exp Dermatol 25:143-6|
|Crawley, Scott W; Weck, Meredith L; Grega-Larson, Nathan E et al. (2016) ANKS4B Is Essential for Intermicrovillar Adhesion Complex Formation. Dev Cell 36:190-200|
|Bryant, Andrew J; Carrick, Ryan P; McConaha, Melinda E et al. (2016) Endothelial HIF signaling regulates pulmonary fibrosis-associated pulmonary hypertension. Am J Physiol Lung Cell Mol Physiol 310:L249-62|
|Chen, Jinjing; Wang, Zhen; Hu, Xiangming et al. (2016) BET Inhibition Attenuates Helicobacter pylori-Induced Inflammatory Response by Suppressing Inflammatory Gene Transcription and Enhancer Activation. J Immunol 196:4132-42|
|Guo, Yan; Xiong, Yanhua; Sheng, Quanghu et al. (2016) A micro-RNA expression signature for human NAFLD progression. J Gastroenterol 51:1022-30|
|Zahm, Christopher D; Szulczewski, Joseph M; Leystra, Alyssa A et al. (2016) Advanced Intestinal Cancers often Maintain a Multi-Ancestral Architecture. PLoS One 11:e0150170|
|Flyak, Andrew I; Shen, Xiaoli; Murin, Charles D et al. (2016) Cross-Reactive and Potent Neutralizing Antibody Responses in Human Survivors of Natural Ebolavirus Infection. Cell 164:392-405|
Showing the most recent 10 out of 1383 publications