Regulation of cell function and identity by cellular senescence

被引:2
作者
Huna, Anda [1 ]
Massemin, Amelie [1 ]
Makulyte, Gabriela [1 ]
Flaman, Jean-Michel [1 ]
Martin, Nadine [1 ]
Bernard, David [1 ]
机构
[1] Univ Lyon, CNRS UMR 5286, Equipe Labellisee Ligue Contre Canc, Inserm U1052,Ctr Rech Cancerol Lyon,Ctr Leon Berar, Lyon, France
关键词
ONCOGENE-INDUCED SENESCENCE; LIVER-CANCER; TELOMERASE; CULTURE; GROWTH; TUMORIGENESIS; SURVEILLANCE; MECHANISMS; SECRETION; BARRIER;
D O I
10.1083/jcb.202401112
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Huna et al. provide insights into the shifting perception of cellular senescence: from a mere cell proliferation arrest to a reinforcement or change of cell identity. During aging and in some contexts, like embryonic development, wound healing, and diseases such as cancer, senescent cells accumulate and play a key role in different pathophysiological functions. A long-held belief was that cellular senescence decreased normal cell functions, given the loss of proliferation of senescent cells. This view radically changed following the discovery of the senescence-associated secretory phenotype (SASP), factors released by senescent cells into their microenvironment. There is now accumulating evidence that cellular senescence also promotes gain-of-function effects by establishing, reinforcing, or changing cell identity, which can have a beneficial or deleterious impact on pathophysiology. These effects may involve both proliferation arrest and autocrine SASP production, although they largely remain to be defined. Here, we provide a historical overview of the first studies on senescence and an insight into emerging trends regarding the effects of senescence on cell identity.
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页数:9
相关论文
共 71 条
  • [1] Chemokine signaling via the CXCR2 receptor reinforces senescence
    Acosta, Juan C.
    O'Loghlen, Ana
    Banito, Ana
    Guijarro, Maria V.
    Augert, Arnaud
    Raguz, Selina
    Fumagalli, Marzia
    Da Costa, Marco
    Brown, Celia
    Popov, Nikolay
    Takatsu, Yoshihiro
    Melamed, Jonathan
    di Fagagna, Fabrizio d'Adda
    Bernard, David
    Hernando, Eva
    Gil, Jesus
    [J]. CELL, 2008, 133 (06) : 1006 - 1018
  • [2] A complex secretory program orchestrated by the inflammasome controls paracrine senescence
    Acosta, Juan Carlos
    Banito, Ana
    Wuestefeld, Torsten
    Georgilis, Athena
    Janich, Peggy
    Morton, Jennifer P.
    Athineos, Dimitris
    Kang, Tae-Won
    Lasitschka, Felix
    Andrulis, Mindaugas
    Pascual, Gloria
    Morris, Kelly J.
    Khan, Sadaf
    Jin, Hong
    Dharmalingam, Gopuraja
    Snijders, Ambrosius P.
    Carroll, Thomas
    Capper, David
    Pritchard, Catrin
    Inman, Gareth J.
    Longerich, Thomas
    Sansom, Owen J.
    Aznar Benitah, Salvador
    Zender, Lars
    Gil, Jesus
    [J]. NATURE CELL BIOLOGY, 2013, 15 (08) : 978 - U221
  • [3] Chronic expression of p16INK4a in the epidermis induces Wnt-mediated hyperplasia and promotes tumor initiation
    Azazmeh, Narmen
    Assouline, Benjamin
    Winter, Eitan
    Ruppo, Shmuel
    Nevo, Yuval
    Maly, Alexander
    Meir, Karen
    Witkiewicz, Agnieszka K.
    Cohen, Jonathan
    Rizou, Sophia, V
    Pikarsky, Eli
    Luxenburg, Chen
    Gorgoulis, Vassilis G.
    Ben-Porath, Ittai
    [J]. NATURE COMMUNICATIONS, 2020, 11 (01)
  • [4] Senescence impairs successful reprogramming to pluripotent stem cells
    Banito, Ana
    Rashid, Sheikh T.
    Acosta, Juan Carlos
    Li, SiDe
    Pereira, Carlos F.
    Geti, Imbisaat
    Pinho, Sandra
    Silva, Jose C.
    Azuara, Veronique
    Walsh, Martin
    Vallier, Ludovic
    Gil, Jesus
    [J]. GENES & DEVELOPMENT, 2009, 23 (18) : 2134 - 2139
  • [5] A Senescence-Like Cell-Cycle Arrest Occurs During Megakaryocytic Maturation: Implications for Physiological and Pathological Megakaryocytic Proliferation
    Besancenot, Rodolphe
    Chaligne, Ronan
    Tonetti, Carole
    Pasquier, Florence
    Marty, Caroline
    Lecluse, Yann
    Vainchenker, William
    Constantinescu, Stefan N.
    Giraudier, Stephane
    [J]. PLOS BIOLOGY, 2010, 8 (09)
  • [6] Telomere length, stem cells and aging
    Blasco, Maria A.
    [J]. NATURE CHEMICAL BIOLOGY, 2007, 3 (10) : 640 - 649
  • [7] Extension of life-span by introduction of telomerase into normal human cells
    Bodnar, AG
    Ouellette, M
    Frolkis, M
    Holt, SE
    Chiu, CP
    Morin, GB
    Harley, CB
    Shay, JW
    Lichtsteiner, S
    Wright, WE
    [J]. SCIENCE, 1998, 279 (5349) : 349 - 352
  • [8] Oncogene-induced senescence as an initial barrier in lymphoma development
    Braig, M
    Lee, S
    Loddenkemper, C
    Rudolph, C
    Peters, AHFM
    Schlegelberger, B
    Stein, H
    Dörken, B
    Jenuwein, T
    Schmitt, CA
    [J]. NATURE, 2005, 436 (7051) : 660 - 665
  • [9] Senescent cells, tumor suppression, and organismal aging: Good citizens, bad neighbors
    Campisi, J
    [J]. CELL, 2005, 120 (04) : 513 - 522
  • [10] SENESCENCE-LIKE GROWTH ARREST INDUCED BY HYDROGEN-PEROXIDE IN HUMAN-DIPLOID FIBROBLAST F65 CELLS
    CHEN, Q
    AMES, BN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) : 4130 - 4134