The broad, long term objective of this application is to obtain funds to purchase a new JEOL JEM-1400 transmission electron microscope (TEM) for the Electron Microscopy Research Laboratory (EMRL) at the University of Kansas Medical Center (KUMC). This core facility has been in operation since 1972, and has received annual financial support from KUMC continuously. The EMRL has superb, experienced technical staff and contains all of the necessary ancillary equipment to carry out a wide range of experiments using TEM and scanning electron microscopy (SEM). However, the only operative TEM instrument available is a JEOL JEM-100CX II that is more than 24 years old. This microscope is now obsolete. Several NIH-funded teams researching a diverse set of health-related topics currently rely on the EMRL at KUMC. These include projects that address mechanisms of (a) normal kidney glomerular capillary development and defects leading to loss of filtration barrier properties;(b) formation of neuronal synapses;(c) intestinal dysmotility and bacterial overgrowth in cystic fibrosis;(d) damage induced by oxidative stress in aging muscle and brain;(e) somatic cell-gonadal germ cell interactions critical for fertility;(f) composition and functions of the bacterial cytoskeleton important for cell division;(g) pathogenesis of HIV-AIDS in a primate model;and (f) anti-cancer activity of select fatty acids on human breast cancer cells. Progress on all of these projects will be enhanced with the availability of a reliable, modern TEM, and throughput will also be increased with access to the requested AMT digital camera system and 5 sample grid holder.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR027564-01
Application #
7795386
Study Section
Special Emphasis Panel (ZRG1-CB-Q (30))
Program Officer
Levy, Abraham
Project Start
2010-01-28
Project End
2011-01-27
Budget Start
2010-01-28
Budget End
2011-01-27
Support Year
1
Fiscal Year
2010
Total Cost
$417,792
Indirect Cost
Name
University of Kansas
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Duncan, Francesca E; Jasti, Susmita; Paulson, Ariel et al. (2017) Age-associated dysregulation of protein metabolism in the mammalian oocyte. Aging Cell 16:1381-1393
New, Jacob; Arnold, Levi; Ananth, Megha et al. (2017) Secretory Autophagy in Cancer-Associated Fibroblasts Promotes Head and Neck Cancer Progression and Offers a Novel Therapeutic Target. Cancer Res 77:6679-6691
Tan, Ee Phie; McGreal, Steven R; Graw, Stefan et al. (2017) Sustained O-GlcNAcylation reprograms mitochondrial function to regulate energy metabolism. J Biol Chem 292:14940-14962
Zhou, Yan; Li, Yuan; Ni, Hong-Min et al. (2016) Nrf2 but not autophagy inhibition is associated with the survival of wild-type epidermal growth factor receptor non-small cell lung cancer cells. Toxicol Appl Pharmacol 310:140-149
Yang, Hua; Ni, Hong-Min; Guo, Fengli et al. (2016) Sequestosome 1/p62 Protein Is Associated with Autophagic Removal of Excess Hepatic Endoplasmic Reticulum in Mice. J Biol Chem 291:18663-74
Li, Yuan; McGreal, Steven; Zhao, Jean et al. (2016) A cell-based quantitative high-throughput image screening identified novel autophagy modulators. Pharmacol Res 110:35-49
Ni, Hong-Min; McGill, Mitchell R; Chao, Xiaojuan et al. (2016) Caspase Inhibition Prevents Tumor Necrosis Factor-?-Induced Apoptosis and Promotes Necrotic Cell Death in Mouse Hepatocytes in Vivo and in Vitro. Am J Pathol 186:2623-36
Briley, Shawn M; Jasti, Susmita; McCracken, Jennifer M et al. (2016) Reproductive age-associated fibrosis in the stroma of the mammalian ovary. Reproduction 152:245-260
Navakanitworakul, Raphatphorn; Hung, Wei-Ting; Gunewardena, Sumedha et al. (2016) Characterization and Small RNA Content of Extracellular Vesicles in Follicular Fluid of Developing Bovine Antral Follicles. Sci Rep 6:25486
Lui, Asona; New, Jacob; Ogony, Joshua et al. (2016) Everolimus downregulates estrogen receptor and induces autophagy in aromatase inhibitor-resistant breast cancer cells. BMC Cancer 16:487

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