Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells
Evidence from animal studies suggests that stress-induced increases in Nrf2-regulated antioxidant gene expression, a critical mechanism of cellular protection, declines with aging. This study examined whether this also occurs in humans. We measured the basal and inducible levels of Nrf2-regulated an...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2018-04-01
|
Series: | Redox Biology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2213231717306067 |
id |
doaj-4868ae9caa554986a8aa98a4675f3365 |
---|---|
record_format |
Article |
spelling |
doaj-4868ae9caa554986a8aa98a4675f33652020-11-24T20:42:54ZengElsevierRedox Biology2213-23172018-04-01143540Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cellsLulu Zhou0Hongqiao Zhang1Kelvin J.A. Davies2Henry Jay Forman3Andrus Gerontology Center of the Leonard Davis School of Gerontology, University of Southern California, 3715 McClintock Ave GER306A, Los Angeles, CA 90089-0191, USAAndrus Gerontology Center of the Leonard Davis School of Gerontology, University of Southern California, 3715 McClintock Ave GER306A, Los Angeles, CA 90089-0191, USAAndrus Gerontology Center of the Leonard Davis School of Gerontology, University of Southern California, 3715 McClintock Ave GER306A, Los Angeles, CA 90089-0191, USA; Division of Molecular & Computational Biology, Department of Biological Sciences, Dornsife College of Letters, Arts, and Sciences, University of Southern California, 3715 McClintock Ave, Los Angeles, CA 90089-0191, USAAndrus Gerontology Center of the Leonard Davis School of Gerontology, University of Southern California, 3715 McClintock Ave GER306A, Los Angeles, CA 90089-0191, USA; Corresponding author.Evidence from animal studies suggests that stress-induced increases in Nrf2-regulated antioxidant gene expression, a critical mechanism of cellular protection, declines with aging. This study examined whether this also occurs in humans. We measured the basal and inducible levels of Nrf2-regulated antioxidant genes in human bronchial epithelial (HBE) cells from subjects of young adult (21â29 years) and older (60â69 years) non-smokers, and explored factors affecting expresion. The basal expression of three representative Nrf2-regulated genes, the catalytic and modulator subunits of glutamate cysteine ligase (GCLC and GCLM, respectively), and NAD(P)H quinone oxidoreductase 1 (NQO1), was higher in cells from the older donors compared with cells from the young adult donors. Upon exposure to the Nrf2 activator, sulforaphane (SF), the expression of these antioxidant genes was increased in cells from both the young adults and the older donors; however, the induction by SF in older donor cells was significantly less than that seen in young adult cells. In addition, the activation of an EpRE-driven reporter by SF was lower in cells from older donors compared to cells from young adults. The basal expression of Nrf2 protein was also lower in cells from older donors than cells from young adults. Furthermore, we found that the basal expression of both Bach1 and c-Myc, two Nrf2 suppressors, was higher in cells from older adults than from young adult donors. In summary, our data suggest that, as in other species, basal expression of Nrf2-regulated genes increases with aging, while inducibility declines with aging. The increased expression of Nrf2 suppressors such as Bach1 and c-Myc may contribute to the impaired inducibility of the Nrf2-regulated antioxidant genes with aging in human bronchial epithelial cells.http://www.sciencedirect.com/science/article/pii/S2213231717306067 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lulu Zhou Hongqiao Zhang Kelvin J.A. Davies Henry Jay Forman |
spellingShingle |
Lulu Zhou Hongqiao Zhang Kelvin J.A. Davies Henry Jay Forman Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells Redox Biology |
author_facet |
Lulu Zhou Hongqiao Zhang Kelvin J.A. Davies Henry Jay Forman |
author_sort |
Lulu Zhou |
title |
Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells |
title_short |
Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells |
title_full |
Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells |
title_fullStr |
Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells |
title_full_unstemmed |
Aging-related decline in the induction of Nrf2-regulated antioxidant genes in human bronchial epithelial cells |
title_sort |
aging-related decline in the induction of nrf2-regulated antioxidant genes in human bronchial epithelial cells |
publisher |
Elsevier |
series |
Redox Biology |
issn |
2213-2317 |
publishDate |
2018-04-01 |
description |
Evidence from animal studies suggests that stress-induced increases in Nrf2-regulated antioxidant gene expression, a critical mechanism of cellular protection, declines with aging. This study examined whether this also occurs in humans. We measured the basal and inducible levels of Nrf2-regulated antioxidant genes in human bronchial epithelial (HBE) cells from subjects of young adult (21â29 years) and older (60â69 years) non-smokers, and explored factors affecting expresion. The basal expression of three representative Nrf2-regulated genes, the catalytic and modulator subunits of glutamate cysteine ligase (GCLC and GCLM, respectively), and NAD(P)H quinone oxidoreductase 1 (NQO1), was higher in cells from the older donors compared with cells from the young adult donors. Upon exposure to the Nrf2 activator, sulforaphane (SF), the expression of these antioxidant genes was increased in cells from both the young adults and the older donors; however, the induction by SF in older donor cells was significantly less than that seen in young adult cells. In addition, the activation of an EpRE-driven reporter by SF was lower in cells from older donors compared to cells from young adults. The basal expression of Nrf2 protein was also lower in cells from older donors than cells from young adults. Furthermore, we found that the basal expression of both Bach1 and c-Myc, two Nrf2 suppressors, was higher in cells from older adults than from young adult donors. In summary, our data suggest that, as in other species, basal expression of Nrf2-regulated genes increases with aging, while inducibility declines with aging. The increased expression of Nrf2 suppressors such as Bach1 and c-Myc may contribute to the impaired inducibility of the Nrf2-regulated antioxidant genes with aging in human bronchial epithelial cells. |
url |
http://www.sciencedirect.com/science/article/pii/S2213231717306067 |
work_keys_str_mv |
AT luluzhou agingrelateddeclineintheinductionofnrf2regulatedantioxidantgenesinhumanbronchialepithelialcells AT hongqiaozhang agingrelateddeclineintheinductionofnrf2regulatedantioxidantgenesinhumanbronchialepithelialcells AT kelvinjadavies agingrelateddeclineintheinductionofnrf2regulatedantioxidantgenesinhumanbronchialepithelialcells AT henryjayforman agingrelateddeclineintheinductionofnrf2regulatedantioxidantgenesinhumanbronchialepithelialcells |
_version_ |
1716821320461713408 |