This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This core facility supports the research of the COBRE investigators. Specifically, high-resolution electrospray-quadrupole/time-of-flight mass spectrometer is being used in Project 2 (Porter) for identification of pro-inflammatory arachidonic acid metabolites generated following stimulation of neuroinflammatory calcitonin gene-related peptide receptor, and to quantitate the amount of prostaglandin compounds hypothesized to be produced from an increased expression of cyclooxygenase-2. In Project 3 (Picklo), mass spectrometry is being used to study mechanisms of 4-hydroxy-2(E)-nonenal (HNE) methabolism in the central nervous system tissue, electrospray-triple quadrupole mass spectrometer will be used to identify and quantitate HNE methabolites, and electrospray-quadrupole/time-of-flight mass spectrometer will be used to identify novel detoxification enzymes. In Project 4 (Murphy), electrospray-triple quadrupole and gas chromatography-ion trap mass spectrometer is being used to measure phospholipids head group flux and turnover in neuronal, astroglia, and stably transfected HEK-293 cell lines, and to measure labeled and unlabeled phospholipids to study the kinetics of compound incorporation. The core facility consists of three instruments; electrospray-quadrupole/time-of-flight, electrospray-triple quadrupole and gas chromatography-ion trap mass spectrometer. These instruments provide us a capability of determining chemical structures of a wide variety of compounds generated in this COBRE as well as a capability of quantifying the compounds. The facility responsibilities (training users and helping with data analysis, operation and maintenance, assuring that the standard operating procedures are followed) will be divided between the facility director and the research assistant.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR017699-05
Application #
7381904
Study Section
Special Emphasis Panel (ZRR1-RI-A (01))
Project Start
2006-07-01
Project End
2007-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
5
Fiscal Year
2006
Total Cost
$261,992
Indirect Cost
Name
University of North Dakota
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
102280781
City
Grand Forks
State
ND
Country
United States
Zip Code
58202
Kulas, Joshua A; Puig, Kendra L; Combs, Colin K (2017) Amyloid precursor protein in pancreatic islets. J Endocrinol 235:49-67
Krout, Danielle; Pramod, Akula Bala; Dahal, Rejwi Acharya et al. (2017) Inhibitor mechanisms in the S1 binding site of the dopamine transporter defined by multi-site molecular tethering of photoactive cocaine analogs. Biochem Pharmacol 142:204-215
Sukumaran, Pramod; Schaar, Anne; Sun, Yuyang et al. (2016) Functional role of TRP channels in modulating ER stress and Autophagy. Cell Calcium 60:123-32
Puig, Kendra L; Kulas, Joshua A; Franklin, Whitney et al. (2016) The Ames dwarf mutation attenuates Alzheimer's disease phenotype of APP/PS1 mice. Neurobiol Aging 40:22-40
Liu, Qing Yan; Koukiekolo, Roger; Zhang, Dong Ling et al. (2016) Molecular events linking cholesterol to Alzheimer's disease and inclusion body myositis in a rabbit model. Am J Neurodegener Dis 5:74-84
Moritz, Amy E; Rastedt, Danielle E; Stanislowski, Daniel J et al. (2015) Reciprocal Phosphorylation and Palmitoylation Control Dopamine Transporter Kinetics. J Biol Chem 290:29095-105
Zhou, Xikun; Ye, Yan; Sun, Yuyang et al. (2015) Transient Receptor Potential Channel 1 Deficiency Impairs Host Defense and Proinflammatory Responses to Bacterial Infection by Regulating Protein Kinase C? Signaling. Mol Cell Biol 35:2729-39
Zhang, Shuang; Yu, Min; Guo, Qiang et al. (2015) Annexin A2 binds to endosomes and negatively regulates TLR4-triggered inflammatory responses via the TRAM-TRIF pathway. Sci Rep 5:15859
Puig, Kendra L; Lutz, Brianna M; Urquhart, Siri A et al. (2015) Overexpression of mutant amyloid-? protein precursor and presenilin 1 modulates enteric nervous system. J Alzheimers Dis 44:1263-78
Rojanathammanee, Lalida; Floden, Angela M; Manocha, Gunjan D et al. (2015) Attenuation of microglial activation in a mouse model of Alzheimer's disease via NFAT inhibition. J Neuroinflammation 12:42

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