The overall objectives of the Gastrointestinal Immunology Core Laboratory are to provide assays of gastrointestinal or hepatic immune function relevant to GI research to Digestive Diseases Center (DDC) investigators, to make available specialized cell sorting and quantitative cytokine laboratory facilities to GI researchers, and to develop new quantitative tests for the evaluation of mRNA and protein for cytokines or other inflammatory mediators that may be useful in clinical and basic research. Major core services include: (1) state-of-the-art techniques in flow cytometry, rare event analysis and high-speed cell sorting; (2) isolation of immune/inflammatory cells from the gastrointestinal tract and liver, (3) quantitative RT-PCR and gene expression analysis for cytokines and other inflammatory mediators, (4) analysis of cytokine protein and cytokine-producing cells, and (5) functional analysis of gastrointestinal immune and inflammatory cells or factors. The core will also provide training and technical advice to researchers interested in developing sophistical immunology procedures for their GI-related research projects. For example, studies on the immunopathologies of disease in the gastrointestinal tract or liver in humans or animal models; development of gene array techniques relevant to immunity and inflammation or; approaches to assess and characterize the host response in normal tissue or a specific model of GI disease. Thus, the Core will benefit the Center members with a regular service and exchange of information in order to facilitate GI research development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
3P30DK056338-02S1
Application #
6655203
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2002-03-01
Project End
2003-02-28
Budget Start
Budget End
Support Year
2
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Mindikoglu, Ayse L; Pappas, Stephen C (2018) Predictors of Response to Terlipressin in Hepatorenal Syndrome. Clin Gastroenterol Hepatol 16:1174
Yu, Wangie; Chen, Yunyun; Dubrulle, Julien et al. (2018) Cisplatin generates oxidative stress which is accompanied by rapid shifts in central carbon metabolism. Sci Rep 8:4306
VanWagner, Lisa B; Kanwal, Fasiha (2018) Hepatology in a changing health care landscape: A call for health services research. Hepatology 68:1154-1162
Zhou, Yong; Hancock, John F (2018) Electron microscopy combined with spatial analysis: quantitative mapping of the nano-assemblies of plasma membrane-associating proteins and lipids. Biophys Rep 4:320-328
Rajan, Anubama; Vela, Lucy; Zeng, Xi-Lei et al. (2018) Novel Segment- and Host-Specific Patterns of Enteroaggregative Escherichia coli Adherence to Human Intestinal Enteroids. MBio 9:
Cash, Brooks D (2018) Understanding and Managing IBS and CIC in the Primary Care Setting. Gastroenterol Hepatol (N Y) 14:3-15
Kennedy, Elizabeth A; King, Katherine Y; Baldridge, Megan T (2018) Mouse Microbiota Models: Comparing Germ-Free Mice and Antibiotics Treatment as Tools for Modifying Gut Bacteria. Front Physiol 9:1534
Zou, Winnie Y; El-Serag, Hashem B; Sada, Yvonne H et al. (2018) Determinants and Outcomes of Hospice Utilization Among Patients with Advance-Staged Hepatocellular Carcinoma in a Veteran Affairs Population. Dig Dis Sci 63:1173-1181
Ramani, Sasirekha; Crawford, Sue E; Blutt, Sarah E et al. (2018) Human organoid cultures: transformative new tools for human virus studies. Curr Opin Virol 29:79-86
Blutt, Sarah E (2018) The Next MacGyver: A Platform to Study Intestinal Organoids Using High-Throughput Computer-Driven Microinjection. Cell Mol Gastroenterol Hepatol 6:352-353

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