2018
DOI: 10.1016/j.jdermsci.2018.05.003
|View full text |Cite|
|
Sign up to set email alerts
|

Proteome-wide changes in primary skin keratinocytes exposed to diesel particulate extract—A role for antioxidants in skin health

Abstract: Our study highlights distinct adverse effects of chronic exposure to DPE/DPE vapor on skin keratinocytes and the potential role of vitamin E in alleviating adverse effects of environmental pollution.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
28
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 27 publications
(28 citation statements)
references
References 71 publications
(29 reference statements)
0
28
0
Order By: Relevance
“…In 3D HEE models, PM usually in concentrations of up to 50 μg/mL was mainly applied topically and short-term exposures (i.e., 24 to 48 h) were performed [128,130,132,133]. PM was shown to affect the physical epidermal barrier in 3D models, as indicated by altered expression of proteins important for epidermal differentiation, such as filaggrin, involucrin, loricrin, and keratins [125,127,129,130,132,133]. Additionally, markers for proliferation, such as Ki67, 5-bromo-2′-deoxyuridine (BrdU) incorporation, and proliferating cell nuclear antigen (PCNA), were shown to be decreased upon PM exposure [125,130].…”
Section: Physical Barriermentioning
confidence: 99%
“…In 3D HEE models, PM usually in concentrations of up to 50 μg/mL was mainly applied topically and short-term exposures (i.e., 24 to 48 h) were performed [128,130,132,133]. PM was shown to affect the physical epidermal barrier in 3D models, as indicated by altered expression of proteins important for epidermal differentiation, such as filaggrin, involucrin, loricrin, and keratins [125,127,129,130,132,133]. Additionally, markers for proliferation, such as Ki67, 5-bromo-2′-deoxyuridine (BrdU) incorporation, and proliferating cell nuclear antigen (PCNA), were shown to be decreased upon PM exposure [125,130].…”
Section: Physical Barriermentioning
confidence: 99%
“…Cellular ROS production has been shown to mediate PM‐induced cytokine production in cultured primary keratinocytes . Oxidative stress responses were also observed in HaCaT cells exposed to concentrated air particles and in primary human keratinocytes exposed to cigarette smoke condensate or diesel particulate extract . Clinical evidence for an oxidative stress response occurring in humans after exposure to pollutants comes from two prospective clinical studies comparing the impact of pollution on subjects living in Mexico City ( N = 96) and Cuernavaca ( N = 93) or in urban ( N = 79) and rural ( N = 80) areas of Shanghai .…”
Section: Biochemical Changes and Molecular Mechanisms Induced By Pollmentioning
confidence: 99%
“…Diesel particulate extract (DPE) has been shown to induce cell death in different cell types, including keratinocytes (KC) [4]. We first determined what concentration of DPE alters KC growth in our experimental conditions.…”
Section: Diesel Particulate Extract (Dpe) Induces Keratinocytes (Kc) mentioning
confidence: 99%
“…Recent evidence reveals that air pollutants lead to impairment of epidermal barrier function; and diesel particulate extract (DPE) is one of the major components of air pollution, as it is the most abundant combustion-derived particle in traffic emission [2,3]. DPE consists of a heterogeneous mixture of volatile components, including aldehydes, benzene, butadiene, polyaromatic hydrocarbons (PAHs) and their derivatives [4]. Prior studies have demonstrated that cellular mechanisms underlying DPE-mediated detrimental effects are mainly initiated by the generation of oxidative stress [5].…”
Section: Introductionmentioning
confidence: 99%