Core C will develop new approaches and provide a range of functional assays that are highly relevant to studies of aging and healthspan in invertebrate model organisms, with a primary focus on Saccharomyces cerevisiae, Caenorhabditis elegans, and Drosophila melanogaster. We will make readily available methods, tools, and expertise for analyzing longevity and healthspan in the common invertebrate model organisms used for aging-related studies. This includes extensive measures for determining longevity and healthspan in budding yeast, Caenorhabditis elegans, and Drosophila melanogaster. We will develop and implement novel, microfluidic approaches to quantify age-related parameters, including lifespan, healthspan, reproduction, gene expression, and protein localization in both budding yeast and C. elegans. Cutting-edge stereolithographic 3D printing technology will be used to develop and disseminate the first 3D printable microfluidic device for aging- related studies. These resources will allow investigators to more rapidly and efficiently assess effects of genetic, pharmacologic, and environmental interventions on key parameters of healthspan and physiology in order to accelerate the understanding of their effects on organismal aging. These tools will be made broadly available to the research community in order to accelerate the use of Invertebrate models in geroscience discovery.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG013280-23
Application #
9316409
Study Section
Special Emphasis Panel (ZAG1)
Project Start
Project End
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
23
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Washington
Department
Pathology
Type
Schools of Medicine
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
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Kramer, Philip A; Duan, Jicheng; Gaffrey, Matthew J et al. (2018) Fatiguing contractions increase protein S-glutathionylation occupancy in mouse skeletal muscle. Redox Biol 17:367-376
Kaeberlein, Matt (2018) How healthy is the healthspan concept? Geroscience 40:361-364
Crane, Matthew M; Kaeberlein, Matt (2018) The paths of mortality: how understanding the biology of aging can help explain systems behavior of single cells. Curr Opin Syst Biol 8:25-31
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Andeen, Nicole K; Yang, Han-Yin; Dai, Dao-Fu et al. (2018) DnaJ Homolog Subfamily B Member 9 Is a Putative Autoantigen in Fibrillary GN. J Am Soc Nephrol 29:231-239
Urfer, Silvan R; Kaeberlein, Tammi L; Mailheau, Susan et al. (2017) Asymptomatic heart valve dysfunction in healthy middle-aged companion dogs and its implications for cardiac aging. Geroscience 39:43-50
Mendenhall, Alexander; Crane, Matthew M; Leiser, Scott et al. (2017) Environmental Canalization of Life Span and Gene Expression in Caenorhabditis elegans. J Gerontol A Biol Sci Med Sci 72:1033-1037
Beaupere, Carine; Wasko, Brian M; Lorusso, Jared et al. (2017) CAN1 Arginine Permease Deficiency Extends Yeast Replicative Lifespan via Translational Activation of Stress Response Genes. Cell Rep 18:1884-1892
Urfer, Silvan R; Kaeberlein, Tammi L; Mailheau, Susan et al. (2017) A randomized controlled trial to establish effects of short-term rapamycin treatment in 24 middle-aged companion dogs. Geroscience 39:117-127

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