Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells. / Jantzen, Kim; Møller, Peter; Karottki, Dorina Gabriela; Olsen, Yulia; Bekö, Gabriel; Clausen, Geo; Hersoug, Lars-Georg; Loft, Steffen.

In: Toxicology, Vol. 359-360, 01.06.2016, p. 11-18.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jantzen, K, Møller, P, Karottki, DG, Olsen, Y, Bekö, G, Clausen, G, Hersoug, L-G & Loft, S 2016, 'Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells', Toxicology, vol. 359-360, pp. 11-18. https://doi.org/10.1016/j.tox.2016.06.007

APA

Jantzen, K., Møller, P., Karottki, D. G., Olsen, Y., Bekö, G., Clausen, G., Hersoug, L-G., & Loft, S. (2016). Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells. Toxicology, 359-360, 11-18. https://doi.org/10.1016/j.tox.2016.06.007

Vancouver

Jantzen K, Møller P, Karottki DG, Olsen Y, Bekö G, Clausen G et al. Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells. Toxicology. 2016 Jun 1;359-360:11-18. https://doi.org/10.1016/j.tox.2016.06.007

Author

Jantzen, Kim ; Møller, Peter ; Karottki, Dorina Gabriela ; Olsen, Yulia ; Bekö, Gabriel ; Clausen, Geo ; Hersoug, Lars-Georg ; Loft, Steffen. / Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells. In: Toxicology. 2016 ; Vol. 359-360. pp. 11-18.

Bibtex

@article{9d7f552dff2d421698996f7728f37530,
title = "Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells",
abstract = "Exposure to particles in the fine and ultrafine size range has been linked to induction of low-grade systemic inflammation, oxidative stress and development of cardiovascular diseases. Declining levels of endothelial progenitor cells within systemic circulation have likewise been linked to progression of cardiovascular diseases. The objective was to determine if exposure to fine and ultrafine particles from indoor and outdoor sources, assessed by personal and residential indoor monitoring, is associated with altered levels of endothelial progenitor cells, and whether such effects are related to leukocyte-mediated oxidative stress. The study utilized a cross sectional design performed in 58 study participants from a larger cohort. Levels of circulating endothelial progenitor cells, defined as either late (CD34(+)KDR(+) cells) or early (CD34(+)CD133(+)KDR(+) cells) subsets were measured using polychromatic flow cytometry. We additionally measured production of reactive oxygen species in leukocyte subsets (lymphocytes, monocytes and granulocytes) by flow cytometry using intracellular 2',7'-dichlorofluoroscein. The measurements encompassed both basal levels of reactive oxygen species production and capacity for reactive oxygen species production for each leukocyte subset. We found that the late endothelial progenitor subset was negatively associated with levels of ultrafine particles measured within the participant residences and with reactive oxygen species production capacity in lymphocytes. Additionally, the early endothelial progenitor cell levels were positively associated with a personalised measure of ultrafine particle exposure and negatively associated with both basal and capacity for reactive oxygen species production in lymphocytes and granulocytes, respectively. Our results indicate that exposure to fine and ultrafine particles derived from indoor sources may have adverse effects on human vascular health.",
keywords = "Journal Article",
author = "Kim Jantzen and Peter M{\o}ller and Karottki, {Dorina Gabriela} and Yulia Olsen and Gabriel Bek{\"o} and Geo Clausen and Lars-Georg Hersoug and Steffen Loft",
note = "Copyright {\textcopyright} 2016 The Authors. Published by Elsevier Ireland Ltd.. All rights reserved.",
year = "2016",
month = jun,
day = "1",
doi = "10.1016/j.tox.2016.06.007",
language = "English",
volume = "359-360",
pages = "11--18",
journal = "Toxicology",
issn = "0300-483X",
publisher = "Elsevier Ireland Ltd",

}

RIS

TY - JOUR

T1 - Exposure to ultrafine particles, intracellular production of reactive oxygen species in leukocytes and altered levels of endothelial progenitor cells

AU - Jantzen, Kim

AU - Møller, Peter

AU - Karottki, Dorina Gabriela

AU - Olsen, Yulia

AU - Bekö, Gabriel

AU - Clausen, Geo

AU - Hersoug, Lars-Georg

AU - Loft, Steffen

N1 - Copyright © 2016 The Authors. Published by Elsevier Ireland Ltd.. All rights reserved.

PY - 2016/6/1

Y1 - 2016/6/1

N2 - Exposure to particles in the fine and ultrafine size range has been linked to induction of low-grade systemic inflammation, oxidative stress and development of cardiovascular diseases. Declining levels of endothelial progenitor cells within systemic circulation have likewise been linked to progression of cardiovascular diseases. The objective was to determine if exposure to fine and ultrafine particles from indoor and outdoor sources, assessed by personal and residential indoor monitoring, is associated with altered levels of endothelial progenitor cells, and whether such effects are related to leukocyte-mediated oxidative stress. The study utilized a cross sectional design performed in 58 study participants from a larger cohort. Levels of circulating endothelial progenitor cells, defined as either late (CD34(+)KDR(+) cells) or early (CD34(+)CD133(+)KDR(+) cells) subsets were measured using polychromatic flow cytometry. We additionally measured production of reactive oxygen species in leukocyte subsets (lymphocytes, monocytes and granulocytes) by flow cytometry using intracellular 2',7'-dichlorofluoroscein. The measurements encompassed both basal levels of reactive oxygen species production and capacity for reactive oxygen species production for each leukocyte subset. We found that the late endothelial progenitor subset was negatively associated with levels of ultrafine particles measured within the participant residences and with reactive oxygen species production capacity in lymphocytes. Additionally, the early endothelial progenitor cell levels were positively associated with a personalised measure of ultrafine particle exposure and negatively associated with both basal and capacity for reactive oxygen species production in lymphocytes and granulocytes, respectively. Our results indicate that exposure to fine and ultrafine particles derived from indoor sources may have adverse effects on human vascular health.

AB - Exposure to particles in the fine and ultrafine size range has been linked to induction of low-grade systemic inflammation, oxidative stress and development of cardiovascular diseases. Declining levels of endothelial progenitor cells within systemic circulation have likewise been linked to progression of cardiovascular diseases. The objective was to determine if exposure to fine and ultrafine particles from indoor and outdoor sources, assessed by personal and residential indoor monitoring, is associated with altered levels of endothelial progenitor cells, and whether such effects are related to leukocyte-mediated oxidative stress. The study utilized a cross sectional design performed in 58 study participants from a larger cohort. Levels of circulating endothelial progenitor cells, defined as either late (CD34(+)KDR(+) cells) or early (CD34(+)CD133(+)KDR(+) cells) subsets were measured using polychromatic flow cytometry. We additionally measured production of reactive oxygen species in leukocyte subsets (lymphocytes, monocytes and granulocytes) by flow cytometry using intracellular 2',7'-dichlorofluoroscein. The measurements encompassed both basal levels of reactive oxygen species production and capacity for reactive oxygen species production for each leukocyte subset. We found that the late endothelial progenitor subset was negatively associated with levels of ultrafine particles measured within the participant residences and with reactive oxygen species production capacity in lymphocytes. Additionally, the early endothelial progenitor cell levels were positively associated with a personalised measure of ultrafine particle exposure and negatively associated with both basal and capacity for reactive oxygen species production in lymphocytes and granulocytes, respectively. Our results indicate that exposure to fine and ultrafine particles derived from indoor sources may have adverse effects on human vascular health.

KW - Journal Article

U2 - 10.1016/j.tox.2016.06.007

DO - 10.1016/j.tox.2016.06.007

M3 - Journal article

C2 - 27311922

VL - 359-360

SP - 11

EP - 18

JO - Toxicology

JF - Toxicology

SN - 0300-483X

ER -

ID: 164385342