scholarly journals Cigarette Smoke Induces Cellular Senescence

2006 ◽  
Vol 35 (6) ◽  
pp. 681-688 ◽  
Author(s):  
Toru Nyunoya ◽  
Martha M. Monick ◽  
Aloysius Klingelhutz ◽  
Timur O. Yarovinsky ◽  
Jeffrey R. Cagley ◽  
...  
Biomolecules ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 462
Author(s):  
Ryuta Mikawa ◽  
Tadashi Sato ◽  
Yohei Suzuki ◽  
Hario Baskoro ◽  
Koichiro Kawaguchi ◽  
...  

Senescent cells accumulate in tissues during aging or pathological settings. The semi-genetic or pharmacological targeting of senescent cells revealed that cellular senescence underlies many aspects of the aging-associated phenotype and diseases. We previously reported that cellular senescence contributes to aging- and disease-associated pulmonary dysfunction. We herein report that the elimination of Arf-expressing cells ameliorates cigarette smoke-induced lung pathologies in mice. Cigarette smoke induced the expression of Ink4a and Arf in lung tissue with concomitant increases in lung tissue compliance and alveolar airspace. The elimination of Arf-expressing cells prior to cigarette smoke exposure protected against these changes. Furthermore, the administration of cigarette smoke extract lead to pulmonary dysfunction, which was ameliorated by subsequent senescent cell elimination. Collectively, these results suggest that senescent cells are a potential therapeutic target for cigarette smoking-associated lung disease.


2021 ◽  
Vol 39 (Supplement 1) ◽  
pp. e227
Author(s):  
Mari Ishida ◽  
Keitaro Ueda ◽  
Chiemi Sakai ◽  
Masao Yoshizumi ◽  
Takafumi Ishida

PLoS ONE ◽  
2013 ◽  
Vol 8 (11) ◽  
pp. e80007 ◽  
Author(s):  
Hongwei Yao ◽  
Isaac K. Sundar ◽  
Vera Gorbunova ◽  
Irfan Rahman

2013 ◽  
Vol 305 (10) ◽  
pp. L737-L746 ◽  
Author(s):  
Hiromichi Hara ◽  
Jun Araya ◽  
Saburo Ito ◽  
Kenji Kobayashi ◽  
Naoki Takasaka ◽  
...  

Mitochondria are dynamic organelles that continuously change their shape through fission and fusion. Disruption of mitochondrial dynamics is involved in disease pathology through excessive reactive oxygen species (ROS) production. Accelerated cellular senescence resulting from cigarette smoke exposure with excessive ROS production has been implicated in the pathogenesis of chronic obstructive pulmonary disease (COPD). Hence, we investigated the involvement of mitochondrial dynamics and ROS production in terms of cigarette smoke extract (CSE)-induced cellular senescence in human bronchial epithelial cells (HBEC). Mitochondrial morphology was examined by electron microscopy and fluorescence microscopy. Senescence-associated β-galactosidase staining and p21 Western blotting of primary HBEC were performed to evaluate cellular senescence. Mitochondrial-specific superoxide production was measured by MitoSOX staining. Mitochondrial fragmentation was induced by knockdown of mitochondrial fusion proteins (OPA1 or Mitofusins) by small-interfering RNA transfection. N-acetylcysteine and Mito-TEMPO were used as antioxidants. Mitochondria in bronchial epithelial cells were prone to be more fragmented in COPD lung tissues. CSE induced mitochondrial fragmentation and mitochondrial ROS production, which were responsible for acceleration of cellular senescence in HBEC. Mitochondrial fragmentation induced by knockdown of fusion proteins also increased mitochondrial ROS production and percentages of senescent cells. HBEC senescence and mitochondria fragmentation in response to CSE treatment were inhibited in the presence of antioxidants. CSE-induced mitochondrial fragmentation is involved in cellular senescence through the mechanism of mitochondrial ROS production. Hence, disruption of mitochondrial dynamics may be a part of the pathogenic sequence of COPD development.


2009 ◽  
Vol 179 (4) ◽  
pp. 279-287 ◽  
Author(s):  
Toru Nyunoya ◽  
Martha M. Monick ◽  
Aloysius L. Klingelhutz ◽  
Heather Glaser ◽  
Jeffrey R. Cagley ◽  
...  

2019 ◽  
Author(s):  
Ryuta Mikawa ◽  
Tadashi Sato ◽  
Yohei Suzuki ◽  
Hario Baskoro ◽  
Masataka Sugimoto

AbstractSenescent cells accumulate in tissues during aging or pathological settings. The semi-genetic or pharmacological targeting of senescent cells revealed that cellular senescence underlies many aspects of the aging-associated phenotype and diseases. We previously reported that cellular senescence contributes to aging- and disease-associated pulmonary dysfunction. We herein report that the elimination of Arf-expressing senescent cells ameliorates cigarette smoke-induced lung pathologies in mice. Cigarette smoke induced the expression of Ink4a and Arf in lung tissue with concomitant increases in lung tissue compliance and alveolar airspace. The elimination of Arf-expressing senescent cells prior to cigarette smoke exposure protected against these changes. Furthermore, the administration of cigarette smoke extract lead to pulmonary dysfunction, which was ameliorated by subsequent senescent cell elimination. Collectively, these results suggest that senescent cells are a potential therapeutic target for cigarette smoking-associated lung disease.


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