Environmental tobacco smoke (ETS) or ?secondhand smoke? exposure leads to stress-induced adverse outcomes including cellular senescence and toxicological effects on the lungs associated with systemic injury and inflammation in airway disorders. We have recently reported that ETS disrupts circadian clock function, induces oxidative stress and stimulates abnormal inflammatory responses. REV-ERB? is a critical component of the molecular clock, which regulates the expression of core clock genes, pro-inflammatory and pro-senescent mediators. Our preliminary data suggest that ETS-mediated cellular senescence is dependent on irregular activity of the clock gene nuclear receptor REV-ERB? in the lungs. Our preliminary data further show an impaired DNA repair and inflammatory responses in molecular clock deficient REV-ERB? KO mice, suggesting the involvement of the clock protein REV-ERB? in regulating DNA damage/repair. Further, REV-ERB? agonists reduce ETS-induced levels of pro-inflammatory and pro-senescent mediators. However, the role of molecular clock dysfunction in chronic ETS-mediated DNA damage/repair, cellular senescence, and toxicological effects remains unknown. Sirtuin 1 (SIRT1), a protein/histone deacetylase, is reduced by ETS, resulting in cellular senescence, oxidative stress and abnormal inflammatory responses. Our preliminary data show that SIRT1 regulates REV-ERB? abundance. However, it is not known whether SIRT1 regulates lung cellular senescence and inflammatory responses through a REV-ERB?-dependent mechanism. We hypothesize that ETS disrupts molecular clock function, specifically REV-ERB? abundance, resulting in DNA damage-initiated cellular senescence through a SIRT1-dependent mechanism in pulmonary toxicity. We propose to test this hypothesis by determining the impact of ETS-induced REV-ERB? disruption on cellular senescence, DNA damage/repair, and toxicological responses in a mouse model based on the following three Aims:
Aim 1 : Determine the molecular mechanism through which ETS-mediated disruption of REV- ERB? molecular clock function leads to cellular senescence and senescence-associated inflammatory phenotype (SASP);
Aim 2 : Determine the involvement of REV-ERB? in DNA repair by non-homologous end joining (NHEJ) during cellular senescence following ETS exposure;
and Aim 3 : Determine the role of SIRT1 in regulating REV-ERB? and DNA damage-induced lung cellular senescence following ETS. The outcome of this proposal will unravel the role of the molecular clock in regulating DNA damage-induced lung cellular senescence via a SIRT1-dependent mechanism during the xenobiotic response to ETS exposure. In turn, our outcomes will have great translational potential for the development of pharmacological therapies based on targeting the molecular clock function to ameliorate lung cellular senescence and DNA damage following chronic exposure to ETS.

Public Health Relevance

Molecular clock dysfunction is associated with the systemic effects of lung irritants like environmental tobacco smoke (ETS) exposure, however, the impact of clock dysfunction on ETS-mediated cellular senescence (irreversible growth arrest) and premature lung aging is not known. We will determine the mechanisms by which the molecular clock regulates stress-induced cellular senescence and inflammation, and whether pharmacological augmentation of REV-ERB? and SIRT1 (anti-aging) activity can attenuate the stress-induced senescence caused by chronic ETS exposure. This will have great translational potential in the development of pharmacological approaches to ameliorate premature lung aging in airway disorders by adverse effects of ETS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56ES027012-01A1
Application #
9536975
Study Section
Systemic Injury by Environmental Exposure (SIEE)
Program Officer
Tyson, Frederick L
Project Start
2017-09-01
Project End
2018-08-31
Budget Start
2017-09-01
Budget End
2018-08-31
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Rochester
Department
Public Health & Prev Medicine
Type
School of Medicine & Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Sundar, Isaac K; Sellix, Michael T; Rahman, Irfan (2018) Redox regulation of circadian molecular clock in chronic airway diseases. Free Radic Biol Med 119:121-128
Sundar, Isaac K; Rashid, Kahkashan; Sellix, Michael T et al. (2017) The nuclear receptor and clock gene REV-ERB? regulates cigarette smoke-induced lung inflammation. Biochem Biophys Res Commun 493:1390-1395