Cited by 49Heat shock proteins researchGenetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence

Characterization of the hsp70 response in lymphoblasts from aged and centenarian subjects and differential effects of in vitro zinc supplementation

Ambra, Roberto, Mocchegiani, Eugenio, Giacconi, Robertina, Canali, Raffaella, Rinna, Alessandra, Malavolta, Marco, Virgili, Fabio·2004·Experimental Gerontology

Abstract

Human centenarians attract increasing interest as they hold some still undefined molecular mechanisms resulting in the achievement of exceptional old age. Recent data suggest the ability of centenarians to efficiently counter the increased cellular stress normally associated with ageing. The ubiquitous heat shock (HS) protein HSP70, expressed under the control of the heat shock transcription factor 1 (HSF-1), is recognized as one of the main chaperones associated with cell protection against stresses. In fact, HSP70 protein induction by heat, a classic well characterized cellular stress, was recently reported to be reduced in cells of most aged humans but not in centenarians. In order to investigate the molecular basis of this feature, we analyzed in vitro the time course expression of the hsp70 gene and the activation of HSF-1 in heat treated Epstein Barr virus transformed B-lymphocytes of centenarians. Our study demonstrates that lymphoblasts from centenarians maintain the transcriptional response of hsp70 gene to heat stress similar to young subjects. Such normal induction of hsp70 is associated to higher binding activity of HSF-1 that compensates an age-dependent delay in HSF-1 phosphorylation. Moreover, in vitro zinc supplementation had an age-dependent effect on hsp70 expression, indicating a role for this nutritionally important molecule and suggesting its involvement in cellular stress responses.

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Crossref · 10.1016/j.exger.2004.07.009

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  • The failure to upregulate chaperone transcription with age, at least in the case of hsp70, is due to the inability of HSF to bind the heat shock element on the chaperone gene promoter.

    “The reason behind the failure to upregulate chaperone transcription with age, at least in the case of hsp70, has been narrowed to the inability of HSF to bind the heat shock element on the chaperone gene promoter (Ambra et al., 2004; Heydari et al., 2000; Locke and Tanguay, 1996; Singh et al., 2006).”

    From Protein Homeostasis and Aging: the importance of exquisite quality control (2011) · cites this paper as Ambra et al., 2004

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Authors
Ambra, R., Mocchegiani, E., Giacconi, R., Canali, R., Rinna, A., Malavolta, M., & Virgili, F.
Affiliations
Istituto Nazionale di Ricerca per gli Alimenti e la Nutrizione (IT)
Corresponding author
Ambra, Roberto
Venue
Experimental Gerontology
Publisher
Elsevier BV
Published
2004-10
Volume
39
Issue
10
Pages
1475-1484
ISSN
0531-5565 (ISSN-L)
OpenAlex
W2084695787
Cited by
49
References
1
Citations by year
2023: 3 · 2022: 2 · 2021: 5 · 2020: 1 · 2019: 1 · 2018: 3 · 2017: 2 · 2016: 3 · 2015: 1 · 2014: 1 · 2013: 5
FWCI
1.06
Type
journal article
Language
en
Open access
closed
Locations
  • Experimental Gerontology (publishedVersion)
  • PubMed (publishedVersion)
  • Università Politecnica delle Marche (Università Politecnica delle Marche) (submittedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
Keywords
HSP70, HSF1, centenarians, aging, lymphoblasts, heat stress response, zinc supplementation, HSP70 expression, cellular stress response, molecular chaperones, Epstein-Barr virus-transformed B lymphocytes
MeSH terms
Heat Shock Transcription Factors, Adult, Aged, Aged, 80 and over, Aging, Cell Transformation, Viral, DNA-Binding Proteins, Female, Gene Expression Regulation, Humans, Lymphocytes, Male, Middle Aged, Phosphorylation, Transcription Factors, HSP70 Heat-Shock Proteins, Heat-Shock Response, Zinc Sulfate, Dietary Supplements

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