Cellular Senescence Triggers Altered Circadian Clocks With a Prolonged Period and Delayed Phases.

aging circadian clock oxidative stress senescence

Journal

Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481

Informations de publication

Date de publication:
2021
Historique:
received: 05 12 2020
accepted: 04 01 2021
entrez: 11 2 2021
pubmed: 12 2 2021
medline: 12 2 2021
Statut: epublish

Résumé

Senescent cells, which show the permanent growth arrest in response to various forms of stress, accumulate in the body with the progression of age, and are associated with aging and age-associated diseases. Although the senescent cells are growth arrested, they still demonstrate high metabolic rate and altered gene expressions, indicating that senescent cells are still active. We recently showed that the circadian clock properties, namely phase and period of the cells, are altered with the establishment of replicative senescence. However, whether cellular senescence triggers the alteration of circadian clock properties in the cells is still unknown. In this study we show that the oxidative stress-induced premature senescence induces the alterations of the circadian clock, similar to the phenotypes of the replicative senescent cells. We found that the oxidative stress-induced premature senescent cells display the prolonged period and delayed phases. In addition, the magnitude of these changes intensified over time, indicating that cellular senescence changes the circadian clock properties. Our current results corroborate with our previous findings and further confirm that cellular senescence induces altered circadian clock properties, irrespective of the replicative senescence or the stress-induced premature senescence.

Identifiants

pubmed: 33568972
doi: 10.3389/fnins.2021.638122
pmc: PMC7868379
doi:

Types de publication

Journal Article

Langues

eng

Pagination

638122

Informations de copyright

Copyright © 2021 Ahmed, Nakahata, Shinohara and Bessho.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Curr Biol. 2017 Sep 11;27(17):2652-2660.e4
pubmed: 28844647
Cancer Res. 2007 Apr 1;67(7):3117-26
pubmed: 17409418
J Neurosci. 2012 Nov 14;32(46):16193-202
pubmed: 23152603
Proc Natl Acad Sci U S A. 2020 May 12;117(19):10350-10356
pubmed: 32358201
Trends Endocrinol Metab. 2016 Apr;27(4):192-203
pubmed: 26947521
JCI Insight. 2019 Apr 4;4(7):
pubmed: 30944259
Cell. 2010 Sep 17;142(6):943-53
pubmed: 20832105
Science. 2009 Oct 16;326(5951):437-40
pubmed: 19833968
Science. 2016 Oct 28;354(6311):472-477
pubmed: 27789842
Nature. 2006 Jun 22;441(7096):1011-4
pubmed: 16791200
Elife. 2018 Feb 26;7:
pubmed: 29481323
Cell Cycle. 2011 Dec 1;10(23):4162-9
pubmed: 22101268
J Cell Sci. 2005 Feb 1;118(Pt 3):485-96
pubmed: 15657080
Nat Protoc. 2009;4(12):1798-806
pubmed: 20010931
Nat Cell Biol. 2015 Aug;17(8):1049-61
pubmed: 26147250
NPJ Aging Mech Dis. 2016 Aug 18;2:16017
pubmed: 28721271
Cell. 2008 Jul 25;134(2):329-40
pubmed: 18662547
Mol Cell Endocrinol. 2017 Nov 5;455:83-92
pubmed: 27591812
JCI Insight. 2016 Aug 4;1(12):e87732
pubmed: 27699227
Eur Respir J. 2017 Aug 3;50(2):
pubmed: 28775044
Science. 2016 Nov 25;354(6315):994-999
pubmed: 27885004
Trends Cell Biol. 2020 Dec;30(12):919-922
pubmed: 32978041
Cancer Res. 2006 Jan 15;66(2):794-802
pubmed: 16424011
Nature. 2011 Nov 02;479(7372):232-6
pubmed: 22048312
Cell. 2017 Mar 23;169(1):132-147.e16
pubmed: 28340339
Cell Commun Signal. 2017 May 4;15(1):17
pubmed: 28472950
Proc Natl Acad Sci U S A. 1995 May 9;92(10):4337-41
pubmed: 7753808
Int J Cancer. 2008 Apr 1;122(7):1483-95
pubmed: 18059027
PLoS Biol. 2005 Oct;3(10):e338
pubmed: 16167846
Aging (Albany NY). 2019 Feb 9;11(3):950-973
pubmed: 30738414
Aging Cell. 2016 Jun;15(3):416-27
pubmed: 26890602
Nat Med. 2017 Jun;23(6):775-781
pubmed: 28436958
Cell Physiol Biochem. 2007;20(1-4):45-54
pubmed: 17595514
Cell. 2005 Feb 25;120(4):513-22
pubmed: 15734683
Semin Cancer Biol. 2011 Dec;21(6):354-9
pubmed: 21925603
J Clin Invest. 2018 Apr 2;128(4):1217-1228
pubmed: 29608141
Protein Cell. 2019 May;10(5):370-375
pubmed: 30421359
Circ Res. 2012 Jul 6;111(2):245-59
pubmed: 22773427
Mol Cell. 2017 Jun 15;66(6):789-800
pubmed: 28622524
Nat Med. 2016 Jan;22(1):78-83
pubmed: 26657143
Trends Cell Biol. 2014 Aug;24(8):464-71
pubmed: 24786309
Science. 2009 May 1;324(5927):651-4
pubmed: 19299583
Science. 2017 Mar 31;355(6332):1433-1436
pubmed: 28360329
Endocrinology. 2003 Dec;144(12):5179-83
pubmed: 12960015
Cell Metab. 2016 Jun 14;23(6):965-966
pubmed: 27304496
Cell Death Differ. 2020 Sep;27(9):2681-2696
pubmed: 32346137
Neurobiol Aging. 2008 Mar;29(3):471-7
pubmed: 17129640
J Physiol Sci. 2018 May;68(3):207-219
pubmed: 29460036
Am J Physiol. 1997 Dec;273(6):R1957-64
pubmed: 9435649
Antioxid Redox Signal. 2018 Mar 1;28(7):507-520
pubmed: 28506121
Free Radic Biol Med. 2019 Dec;145:312-320
pubmed: 31585206
Cell. 2009 Oct 2;139(1):199-210
pubmed: 19765810
Nat Cell Biol. 2015 Sep;17(9):1205-17
pubmed: 26280535
Science. 1974 Nov 8;186(4163):548-50
pubmed: 4469680
Science. 2009 May 1;324(5927):654-7
pubmed: 19286518
Nat Commun. 2017 Feb 23;8:14532
pubmed: 28230051
J Biol Chem. 2007 Jul 20;282(29):20794-8
pubmed: 17525164
Exp Gerontol. 2000 Dec;35(9-10):1229-37
pubmed: 11113604
Nature. 2018 Oct;562(7728):578-582
pubmed: 30232451
JCI Insight. 2018 Feb 8;3(3):
pubmed: 29415880
PLoS One. 2013 Dec 02;8(12):e82006
pubmed: 24312621
Nat Neurosci. 2019 May;22(5):719-728
pubmed: 30936558
J Clin Invest. 2004 Nov;114(9):1299-307
pubmed: 15520862
Carcinogenesis. 2015 Oct;36(10):1180-92
pubmed: 26168819
Nat Rev Genet. 2017 Mar;18(3):164-179
pubmed: 27990019
Trends Cell Biol. 2014 Feb;24(2):90-9
pubmed: 23916625
Trends Endocrinol Metab. 2012 Jan;23(1):1-8
pubmed: 22169754
Dev Cell. 2014 Dec 22;31(6):722-33
pubmed: 25499914
Ann N Y Acad Sci. 2000 Jun;908:85-98
pubmed: 10911950
Age (Dordr). 2016 Feb;38(1):26
pubmed: 26867806
Cell. 2017 Oct 5;171(2):321-330.e14
pubmed: 28965763
J Gerontol A Biol Sci Med Sci. 2017 Jun 1;72(6):780-785
pubmed: 27516624
Mol Cell Endocrinol. 2013 Feb 25;366(2):163-9
pubmed: 22750052
Nature. 2016 Feb 11;530(7589):184-9
pubmed: 26840489
Mol Cell Biol. 1999 Mar;19(3):2109-17
pubmed: 10022898
eNeuro. 2015 Sep 22;2(4):
pubmed: 26464996
Nat Commun. 2016 Apr 06;7:11190
pubmed: 27048913
Chronobiol Int. 2018 May;35(5):730-738
pubmed: 29372841
J Proteome Res. 2015 Apr 3;14(4):1854-71
pubmed: 25690941
Genes Cells. 2017 Dec;22(12):982-992
pubmed: 29178516
Chronobiol Int. 1994 Apr;11(2):103-12
pubmed: 8033238
PLoS Genet. 2018 May 11;14(5):e1007369
pubmed: 29750810

Auteurs

Rezwana Ahmed (R)

Laboratory of Gene Regulation Research, Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology (NAIST), Ikoma, Japan.
Department of Neurobiology and Behavior, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Department of Pharmaceutical Sciences, North South University, Dhaka, Bangladesh.

Yasukazu Nakahata (Y)

Laboratory of Gene Regulation Research, Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology (NAIST), Ikoma, Japan.
Department of Neurobiology and Behavior, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Kazuyuki Shinohara (K)

Department of Neurobiology and Behavior, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Yasumasa Bessho (Y)

Laboratory of Gene Regulation Research, Division of Biological Science, Graduate School of Science and Technology, Nara Institute of Science and Technology (NAIST), Ikoma, Japan.

Classifications MeSH