Literature DB >> 6412000

Quantitative measures of aging in the nematode Caenorhabditis elegans: II. Lysosomal hydrolases as markers of senescence.

M A Bolanowski, L A Jacobson, R L Russell.   

Abstract

In an attempt to provide additional quantitative markers of senescence in the nematode Caenorhabditis elegans, we have identified age-dependent increases in four lysosomal enzymes: acid phosphatase, beta-N-acetyl-D-glucosaminidase, beta-D-glucosidase, and alpha-D-mannosidase. These enzymes were judged to be lysosomal on the basis of their resemblance to analogous mammalian lysosomal enzymes with regard to subcellular fractionation, lectin binding, Km, molecular weights, inhibitor sensitivities, and pH optima. In nematode populations which had a median lifespan of 8.9 +/- 0.7 days and a maximum lifespan of 14-16 days, we observed the following increases in acid hydrolase activities per animal from day 3 (early adulthood) to day 10: (1) up to 2.5-fold for acid phosphatase; (2) 8-fold for beta-N-acetyl-D-glucosaminidase; (3) 9-fold for beta-D-glucosidase; and (4) 4-fold for alpha-D-mannosidase. Three forms of acid phosphatase and two forms of beta-D-glucosidase were separated by ion-exchange chromatography, but in each case only one form of the enzyme was primarily responsible for the age-dependent increase in total activity: acid phosphatase I increased 18-fold, while beta-D-glucosidase I increased 100-fold. By contrast, there were only slight age-dependent changes in choline acetyltransferase, acetylcholinesterase, or alpha-D-glucosidase activities after early adulthood. The age-dependent increases in acid phosphatase, beta-N-acetyl-D-glucosaminidase, beta-D-glucosidase, and alpha-D-mannosidase activities are sufficiently large and reproducible to be useful quantitative markers of senescence in C. elegans.

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Year:  1983        PMID: 6412000     DOI: 10.1016/0047-6374(83)90048-9

Source DB:  PubMed          Journal:  Mech Ageing Dev        ISSN: 0047-6374            Impact factor:   5.432


  8 in total

1.  Regulation of proteinase levels in the nematode Caenorhabditis elegans. Preferential depression by acute or chronic starvation.

Authors:  J M Hawdon; S W Emmons; L A Jacobson
Journal:  Biochem J       Date:  1989-11-15       Impact factor: 3.857

2.  Identification of a putative structural gene for cathepsin D in Caenorhabditis elegans.

Authors:  L A Jacobson; L Jen-Jacobson; J M Hawdon; G P Owens; M A Bolanowski; S W Emmons; M V Shah; R A Pollock; D S Conklin
Journal:  Genetics       Date:  1988-06       Impact factor: 4.562

Review 3.  Developmental biomarkers of aging in Caenorhabditis elegans.

Authors:  Zachary Pincus; Frank J Slack
Journal:  Dev Dyn       Date:  2010-05       Impact factor: 3.780

4.  Patterns of metabolic activity during aging of the wild type and longevity mutants of Caenorhabditis elegans.

Authors:  B P Braeckman; K Houthoofd; J R Vanfleteren
Journal:  J Am Aging Assoc       Date:  2000-04

5.  A deletion in the golgi alpha-mannosidase II gene of Caenorhabditis elegans results in unexpected non-wild-type N-glycan structures.

Authors:  Katharina Paschinger; Matthias Hackl; Martin Gutternigg; Dorothea Kretschmer-Lubich; Ute Stemmer; Verena Jantsch; Günter Lochnit; Iain B H Wilson
Journal:  J Biol Chem       Date:  2006-07-24       Impact factor: 5.157

6.  Biosynthesis of truncated N-linked oligosaccharides results from non-orthologous hexosaminidase-mediated mechanisms in nematodes, plants, and insects.

Authors:  Martin Gutternigg; Dorothea Kretschmer-Lubich; Katharina Paschinger; Dubravko Rendić; Josef Hader; Petra Geier; Ramona Ranftl; Verena Jantsch; Günter Lochnit; Iain B H Wilson
Journal:  J Biol Chem       Date:  2007-07-18       Impact factor: 5.157

7.  Lysosome activity is modulated by multiple longevity pathways and is important for lifespan extension in C. elegans.

Authors:  Yanan Sun; Meijiao Li; Dongfeng Zhao; Xin Li; Chonglin Yang; Xiaochen Wang
Journal:  Elife       Date:  2020-06-02       Impact factor: 8.140

8.  Resveratrol targets PD-L1 glycosylation and dimerization to enhance antitumor T-cell immunity.

Authors:  Sara Verdura; Elisabet Cuyàs; Eric Cortada; Joan Brunet; Eugeni Lopez-Bonet; Begoña Martin-Castillo; Joaquim Bosch-Barrera; José Antonio Encinar; Javier A Menendez
Journal:  Aging (Albany NY)       Date:  2020-01-04       Impact factor: 5.682

  8 in total

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