Literature DB >> 29778759

To adapt or not to adapt: Consequences of declining Adaptive Homeostasis and Proteostasis with age.

Laura C D Pomatto1, Patrick Y Sun1, Kelvin J A Davies2.   

Abstract

Many consequences of ageing can be broadly attributed to the inability to maintain homeostasis. Multiple markers of ageing have been identified, including loss of protein homeostasis, increased inflammation, and declining metabolism. Although much effort has been focused on characterization of the ageing phenotype, much less is understood about the underlying causes of ageing. To address this gap, we outline the age-associated consequences of dysregulation of 'Adaptive Homeostasis' and its proposed contributing role as an accelerator of the ageing phenotype. Adaptive Homeostasis is a phenomenon, shared across cells and tissues of both simple and complex organisms, that enables the transient plastic expansion or contraction of the homeostatic range to modulate stress-protective systems (such as the Proteasome, the Immunoproteasome, and the Lon protease) in response to varying internal and external environments. The age-related rise in the baseline of stress-protective systems and the inability to increase beyond a physiological ceiling is likely a contributor to the reduction and loss of Adaptive Homeostasis. We propose that dysregulation of Adaptive Homeostasis in the final third of lifespan is a significant factor in the ageing process, while successful maintenance of Adaptive Homeostasis below a physiological ceiling results in extended longevity.
Copyright © 2018 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aging; Immunoproteasome; Lon protease; Nrf2; Physiological ceiling; Proteasome; Protein aggregates; longevity

Mesh:

Year:  2018        PMID: 29778759      PMCID: PMC6240408          DOI: 10.1016/j.mad.2018.05.006

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


  104 in total

1.  Protein oxidation and degradation during cellular senescence of human BJ fibroblasts: part II--aging of nondividing cells.

Authors:  N Sitte; K Merker; T Von Zglinicki; K J Davies; T Grune
Journal:  FASEB J       Date:  2000-12       Impact factor: 5.191

2.  Protein oxidation and degradation during cellular senescence of human BJ fibroblasts: part I--effects of proliferative senescence.

Authors:  N Sitte; K Merker; T Von Zglinicki; T Grune; K J Davies
Journal:  FASEB J       Date:  2000-12       Impact factor: 5.191

3.  Fibroblast cultures from healthy centenarians have an active proteasome.

Authors:  N Chondrogianni; I Petropoulos; C Franceschi; B Friguet; E S Gonos
Journal:  Exp Gerontol       Date:  2000-09       Impact factor: 4.032

Review 4.  Oxidative modification of proteins during aging.

Authors:  R L Levine; E R Stadtman
Journal:  Exp Gerontol       Date:  2001-09       Impact factor: 4.032

5.  Ubiquitin conjugation is not required for the degradation of oxidized proteins by proteasome.

Authors:  Reshma Shringarpure; Tilman Grune; Jana Mehlhase; Kelvin J A Davies
Journal:  J Biol Chem       Date:  2002-10-24       Impact factor: 5.157

6.  Ezrin turnover and cell shape changes catalyzed by proteasome in oxidatively stressed cells.

Authors:  Tilman Grune; Thomas Reinheckel; James A North; Rui Li; Paloma B Bescos; Reshma Shringarpure; Kelvin J A Davies
Journal:  FASEB J       Date:  2002-10       Impact factor: 5.191

7.  Modulation of Lon protease activity and aconitase turnover during aging and oxidative stress.

Authors:  Daniela A Bota; Holly Van Remmen; Kelvin J A Davies
Journal:  FEBS Lett       Date:  2002-12-04       Impact factor: 4.124

8.  Aggregation of recombinant bovine granulocyte colony stimulating factor in solution.

Authors:  Richard Bartkowski; Ryan Kitchel; Niomi Peckham; Leonid Margulis
Journal:  J Protein Chem       Date:  2002-03

9.  Lon protease preferentially degrades oxidized mitochondrial aconitase by an ATP-stimulated mechanism.

Authors:  Daniela A Bota; Kelvin J A Davies
Journal:  Nat Cell Biol       Date:  2002-09       Impact factor: 28.824

10.  Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases.

Authors:  Monica Bucciantini; Elisa Giannoni; Fabrizio Chiti; Fabiana Baroni; Lucia Formigli; Jesús Zurdo; Niccolò Taddei; Giampietro Ramponi; Christopher M Dobson; Massimo Stefani
Journal:  Nature       Date:  2002-04-04       Impact factor: 49.962

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  5 in total

Review 1.  Ubiquitin carboxyl-terminal hydrolase L-1 in brain: Focus on its oxidative/nitrosative modification and role in brains of subjects with Alzheimer disease and mild cognitive impairment.

Authors:  D Allan Butterfield
Journal:  Free Radic Biol Med       Date:  2021-11-01       Impact factor: 7.376

2.  Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageing.

Authors:  Laura C D Pomatto; Patrick Y Sun; Kelsi Yu; Sandhyarani Gullapalli; Conscience P Bwiza; Christina Sisliyan; Sarah Wong; Hongqiao Zhang; Henry Jay Forman; Peter L Oliver; Kay E Davies; Kelvin J A Davies
Journal:  Redox Biol       Date:  2019-04-14       Impact factor: 11.799

3.  NKT-like (CD3 + CD56+) cells differ from T cells in expression level of cellular protective proteins and sensitivity to stimulation in the process of ageing.

Authors:  Lucyna Kaszubowska; Jerzy Foerster; Zbigniew Kmieć
Journal:  Immun Ageing       Date:  2022-04-11       Impact factor: 6.400

Review 4.  Cancer as a disease of old age: changing mutational and microenvironmental landscapes.

Authors:  Ezio Laconi; Fabio Marongiu; James DeGregori
Journal:  Br J Cancer       Date:  2020-02-11       Impact factor: 7.640

Review 5.  The Puzzling Role of Neuron-Specific PMCA Isoforms in the Aging Process.

Authors:  Tomasz Boczek; Tomasz Radzik; Bozena Ferenc; Ludmila Zylinska
Journal:  Int J Mol Sci       Date:  2019-12-16       Impact factor: 5.923

  5 in total

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