The CF Cell & Tissue Bioassays Core (Core D) is an important component of the UCSF CF Research and Translation Core Center. The major objective of the Core is to test the efficacy of CF-targeted small molecules discovered by high-throughput screening (HTS; performed by Core A) in physiologically relevant pre-clinical assays. This objective is accomplished by performing electrophysiological and optical assays that probe ion channel and epithelial cell function in CF-relevant cell and tissue models. Assays use immortalized cell culture models, primary cell cultures derived from human sources, three-dimensional models including organoids, and tissue samples such as airway fragments from non-CF and CF subjects (provided by Core B, Cell & Tissue Models). The most heavily used resource in the Core are Ussing chambers for analysis of short-circuit current which is performed to validate hits identified by HTS, determine hit efficacy, provide structure-activity relationship data during hit-to-lead optimization, and assess lead efficacy in human airway tissue samples from CF and non-CF subjects. Other major Core D resources include optical assays of CF-relevant airway properties, including measurement of airway surface liquid and submucosal gland secretions in human cell cultures and airway tissues from CF and non-CF subjects. Many of the optical assays provided by Core D were developed to investigate CF lung disease mechanisms and are uniquely available at UCSF. Core D also carries out electrophysiological and optical assays to support basic and translational research on CF pathophysiology and assay development for screening. Of the 25 projects in the research base, 20 will use Core D resources.

Public Health Relevance

A critical step in preclinical development of CF-targeted drugs is assessment of compound efficacy in validated cell and tissue based assays. The major objective of Core D (CF Cell & Tissue Bioassays) of the UCSF CF Research and Translation Core Center is to test efficacy of compounds discovered by our Center in appropriate assays. A secondary goal of the Core is to develop novel assays that will facilitate or improve compound testing.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK072517-14
Application #
9512925
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
14
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
Sun, Dingyuan I; Tasca, Alexia; Haas, Maximilian et al. (2018) Na+/H+ Exchangers Are Required for the Development and Function of Vertebrate Mucociliary Epithelia. Cells Tissues Organs :1-14
Bhakta, Nirav R; Christenson, Stephanie A; Nerella, Srilaxmi et al. (2018) IFN-stimulated Gene Expression, Type 2 Inflammation, and Endoplasmic Reticulum Stress in Asthma. Am J Respir Crit Care Med 197:313-324
Smith, Alex J; Verkman, Alan S (2018) The ""glymphatic"" mechanism for solute clearance in Alzheimer's disease: game changer or unproven speculation? FASEB J 32:543-551
Duan, Tianjiao; Smith, Alex J; Verkman, Alan S (2018) Complement-dependent bystander injury to neurons in AQP4-IgG seropositive neuromyelitis optica. J Neuroinflammation 15:294
Lee, Sujin; Cil, Onur; Diez-Cecilia, Elena et al. (2018) Nanomolar-Potency 1,2,4-Triazoloquinoxaline Inhibitors of the Kidney Urea Transporter UT-A1. J Med Chem 61:3209-3217
Tradtrantip, Lukmanee; Felix, Christian M; Spirig, Rolf et al. (2018) Recombinant IgG1 Fc hexamers block cytotoxicity and pathological changes in experimental in vitro and rat models of neuromyelitis optica. Neuropharmacology 133:345-353
Phuan, Puay-Wah; Veit, Guido; Tan, Joseph-Anthony et al. (2018) ?F508-CFTR Modulator Screen Based on Cell Surface Targeting of a Chimeric Nucleotide Binding Domain 1 Reporter. SLAS Discov 23:823-831
Verkman, Alan S; Yao, Xiaoming; Smith, Alex J (2018) The evolving mystery of why skeletal muscle is spared in seropositive neuromyelitis optica. J Cell Mol Med 22:2039-2040
Tradtrantip, Lukmanee; Yao, Xiaoming; Su, Tao et al. (2017) Bystander mechanism for complement-initiated early oligodendrocyte injury in neuromyelitis optica. Acta Neuropathol 134:35-44
Tradtrantip, Lukmanee; Jin, Bjung-Ju; Yao, Xiaoming et al. (2017) Aquaporin-Targeted Therapeutics: State-of-the-Field. Adv Exp Med Biol 969:239-250

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