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      New label‐free automated survival assays reveal unexpected stress resistance patterns during C. elegans aging

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          Abstract

          Caenorhabditis elegans is an excellent model for high‐throughput experimental approaches but lacks an automated means to pinpoint time of death during survival assays over a short time frame, that is, easy to implement, highly scalable, robust, and versatile. Here, we describe an automated, label‐free, high‐throughput method using death‐associated fluorescence to monitor nematode population survival (dubbed LFASS for label‐free automated survival scoring), which we apply to severe stress and infection resistance assays. We demonstrate its use to define correlations between age, longevity, and severe stress resistance, and its applicability to parasitic nematodes. The use of LFASS to assess the effects of aging on susceptibility to severe stress revealed an unexpected increase in stress resistance with advancing age, which was largely autophagy‐dependent. Correlation analysis further revealed that while severe thermal stress resistance positively correlates with lifespan, severe oxidative stress resistance does not. This supports the view that temperature‐sensitive protein‐handling processes more than redox homeostasis underpin aging in C. elegans. That the ages of peak resistance to infection, severe oxidative stress, heat shock, and milder stressors differ markedly suggests that stress resistance and health span do not show a simple correspondence in C. elegans.

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          Most cited references41

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          Regulation of aging and age-related disease by DAF-16 and heat-shock factor.

          A.-L. Hsu (2003)
          The Caenorhabditis elegans transcription factor HSF-1, which regulates the heat-shock response, also influences aging. Reducing hsf-1 activity accelerates tissue aging and shortens life-span, and we show that hsf-1 overexpression extends lifespan. We find that HSF-1, like the transcription factor DAF-16, is required for daf-2-insulin/IGF-1 receptor mutations to extend life-span. Our findings suggest this is because HSF-1 and DAF-16 together activate expression of specific genes, including genes encoding small heat-shock proteins, which in turn promote longevity. The small heat-shock proteins also delay the onset of polyglutamine-expansion protein aggregation, suggesting that these proteins couple the normal aging process to this type of age-related disease.
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            Caenorhabditis elegans: An Emerging Model in Biomedical and Environmental Toxicology

            The nematode Caenorhabditis elegans has emerged as an important animal model in various fields including neurobiology, developmental biology, and genetics. Characteristics of this animal model that have contributed to its success include its genetic manipulability, invariant and fully described developmental program, well-characterized genome, ease of maintenance, short and prolific life cycle, and small body size. These same features have led to an increasing use of C. elegans in toxicology, both for mechanistic studies and high-throughput screening approaches. We describe some of the research that has been carried out in the areas of neurotoxicology, genetic toxicology, and environmental toxicology, as well as high-throughput experiments with C. elegans including genome-wide screening for molecular targets of toxicity and rapid toxicity assessment for new chemicals. We argue for an increased role for C. elegans in complementing other model systems in toxicological research.
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              Regulation of longevity in Caenorhabditis elegans by heat shock factor and molecular chaperones.

              The correlation between longevity and stress resistance observed in long-lived mutant animals suggests that the ability to sense and respond to environmental challenges could be important for the regulation of life span. We therefore examined the role of heat shock factor (HSF-1), a master transcriptional regulator of stress-inducible gene expression and protein folding homeostasis, in the regulation of longevity. Down-regulation of hsf-1 by RNA interference suppressed longevity of mutants in an insulin-like signaling (ILS) pathway that functions in the nervous system of Caenorhabditis elegans to influence aging. hsf-1 was also required for temperature-induced dauer larvae formation in an ILS mutant. Using tissue-specific expression of wild-type or dominant negative HSF-1, we demonstrated that HSF-1 acts in multiple tissues to regulate longevity. Down-regulation of individual molecular chaperones, transcriptional targets of HSF-1, also decreased longevity of long-lived mutant but not wild-type animals. However, suppression by individual chaperones was to a lesser extent, suggesting an important role for networks of chaperones. The interaction of ILS with HSF-1 could represent an important molecular strategy to couple the regulation of longevity with an ancient genetic switch that governs the ability of cells to sense and respond to stress.
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                Author and article information

                Contributors
                a.benedetto@lancaster.ac.uk
                Journal
                Aging Cell
                Aging Cell
                10.1111/(ISSN)1474-9726
                ACEL
                Aging Cell
                John Wiley and Sons Inc. (Hoboken )
                1474-9718
                1474-9726
                16 July 2019
                October 2019
                : 18
                : 5 ( doiID: 10.1111/acel.v18.5 )
                : e12998
                Affiliations
                [ 1 ] Department of Genetics, Evolution and Environment, Institute of Healthy Ageing University College London London UK
                [ 2 ] Division of Biomedical and Life Sciences Lancaster University Lancaster UK
                [ 3 ] School of Biosciences University of Kent Canterbury UK
                [ 4 ] Division of Infection, Immunity & Respiratory Medicine University of Manchester Manchester UK
                [ 5 ] MRC London Institute of Medical Sciences, Imperial College London London UK
                Author notes
                [*] [* ] Correspondence

                Alexandre Benedetto, FHM, Division of Biomedical and Life Sciences, Furness Building, Lancaster University, Bailrigg, Lancaster LA1 4YW, UK.

                Email: a.benedetto@ 123456lancaster.ac.uk

                Author information
                https://orcid.org/0000-0002-4593-2114
                https://orcid.org/0000-0002-1923-9121
                https://orcid.org/0000-0002-2037-526X
                https://orcid.org/0000-0002-9451-4621
                https://orcid.org/0000-0002-3696-4843
                https://orcid.org/0000-0002-6653-4676
                Article
                ACEL12998
                10.1111/acel.12998
                6718543
                31309734
                5caa950f-7bd9-40e6-9ff5-479b425a4989
                © 2019 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 26 February 2019
                : 15 May 2019
                : 22 May 2019
                Page count
                Figures: 3, Tables: 0, Pages: 10, Words: 6860
                Funding
                Funded by: European Framework Program
                Award ID: FP6-518230
                Funded by: National Institutes of Health
                Award ID: 098565
                Award ID: 12
                Funded by: Wellcome Trust Strategic Award (098565/Z/12/Z) awarded to David Gems
                Award ID: 098565/Z/12/Z
                Funded by: Sart-up grant from Lancaster University awarded to Alexandre Benedetto Wellcome Trust Seed Award in Sciences (214076/Z/18/Z) awarded to Alexandre Benedetto
                Award ID: Start-up package to AB
                Categories
                Original Paper
                Original Paper
                Custom metadata
                2.0
                acel12998
                October 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.9 mode:remove_FC converted:30.09.2019

                Cell biology
                aging,autophagy,c. elegans,infection,stress,survival
                Cell biology
                aging, autophagy, c. elegans, infection, stress, survival

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