The overall mission of this core facility is to provide the necessary equipment and technical support for tissue culture to allow rigorous pursuit of the goals of the Program Project. The rationale for the proposed core is to establish a single laboratory, shared by members of the five groups (Projects 1 through 4 and Core C), which will alleviate duplications in costs of equipment, supplies, and salaries as well as further enhance scientific exchange between the participating labs. Establishment of this core facility will therefore save a substantial amount of research effort and costs for each of the component labs. Importantly, the core facility will also provide several services critical for the development of each project, including: a) Preparation and sterility testing of all cell culture media including specialized formulations and bulk reagents for preparative work. b) Screening serum lots for optimal growth promoting properties. Serum aliquoting and heat inactivation will also be performed. This service will allow for direct comparison of results between different groups without concern for differential serum effects on growth properties of cultured cell lines. c) Testing all cell lines for contamination including mycoplasma, bacteria and fungi. d) Routine maintenance of cell lines, including cell freezing and thawing. This will be an important service for investigators and will allow the rigorous recording of passage numbers. In addition, the facility will provide large scale preparation of cells for biochemical purposes. e) Maintenance of all tissue culture equipment as well as cleaning and periodic decontamination of equipment and facilities. Routine cleaning and decontamination greatly reduces the occurrence of spontaneous contamination detrimental to cell culture work.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Type
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
New, M I; Nimkarn, S; Brandon, D D et al. (2001) Resistance to multiple steroids in two sisters. J Steroid Biochem Mol Biol 76:161-6
Slugg, R M; Hayward, M D; Ronnekleiv, O K et al. (2000) Effect of the mu-opioid agonist DAMGO on medial basal hypothalamic neurons in beta-endorphin knockout mice. Neuroendocrinology 72:208-17
Samuels, M H; Brandon, D D; Isabelle, L M et al. (2000) Cortisol production rates in subjects with suspected Cushing's syndrome: assessment by stable isotope dilution methodology and comparison to other diagnostic methods. J Clin Endocrinol Metab 85:22-8
Coste, S C; Kesterson, R A; Heldwein, K A et al. (2000) Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2. Nat Genet 24:403-9
Grahame, N J; Mosemiller, A K; Low, M J et al. (2000) Naltrexone and alcohol drinking in mice lacking beta-endorphin by site-directed mutagenesis. Pharmacol Biochem Behav 67:759-66
Grisel, J E; Mogil, J S; Grahame, N J et al. (1999) Ethanol oral self-administration is increased in mutant mice with decreased beta-endorphin expression. Brain Res 835:62-7
Brandon, D D; Isabelle, L M; Samuels, M H et al. (1999) Cortisol production rate measurement by stable isotope dilution using gas chromatography-negative ion chemical ionization mass spectrometry. Steroids 64:372-8
New, M I; Nimkarn, S; Brandon, D D et al. (1999) Resistance to several steroids in two sisters. J Clin Endocrinol Metab 84:4454-64
Grahame, N J; Low, M J; Cunningham, C L (1998) Intravenous self-administration of ethanol in beta-endorphin-deficient mice. Alcohol Clin Exp Res 22:1093-8
Abrami, L; Fivaz, M; Decroly, E et al. (1998) The pore-forming toxin proaerolysin is activated by furin. J Biol Chem 273:32656-61

Showing the most recent 10 out of 21 publications