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Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation

Electronic cigarettes (e-cigarettes) are promoted as low-risk alternatives to combustible cigarettes. However, the effects of chronic inhalation of potential toxicants emitted by ecigarettes remain largely unexamined. It is conceivable that smoking-induced chronic diseases result in cellular injury,...

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Autores principales: Shaito, A., Saliba, J., Husari, A., El-Harakeh, M., Chhouri, H., Hashem, Y., Shihadeh, A., El-Sabban, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660168/
https://www.ncbi.nlm.nih.gov/pubmed/29079789
http://dx.doi.org/10.1038/s41598-017-14634-z
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author Shaito, A.
Saliba, J.
Husari, A.
El-Harakeh, M.
Chhouri, H.
Hashem, Y.
Shihadeh, A.
El-Sabban, M.
author_facet Shaito, A.
Saliba, J.
Husari, A.
El-Harakeh, M.
Chhouri, H.
Hashem, Y.
Shihadeh, A.
El-Sabban, M.
author_sort Shaito, A.
collection PubMed
description Electronic cigarettes (e-cigarettes) are promoted as low-risk alternatives to combustible cigarettes. However, the effects of chronic inhalation of potential toxicants emitted by ecigarettes remain largely unexamined. It is conceivable that smoking-induced chronic diseases result in cellular injury, in the absence of effective repair by stem cells. This study evaluates the effect of cigarette and e-cigarette aerosol extracts on the survival and differentiation of bone marrow-derived mesenchymal stem cells (MSCs). MSC growth and osteogenic differentiation were examined after exposure to smoke extracts. Data revealed detrimental effects of both cigarette and e-cigarette extracts on MSC morphology and growth. Levels and activity of alkaline phosphatase, an osteogenic marker, decreased and induction of osteoblastic differentiation was impaired. Both smoke extracts prevented osteogenic differentiation from progressing, evident by decreased expression of terminal osteogenic markers and mineralization. Elevated levels of reactive oxygen species (ROS) were detected in cells exposed to smoke extracts. Moreover, decreased differentiation potential was concomitant with severe down-regulation of Connexin 43 expression, leading to the loss of gap junction-mediated communication, which together with elevated ROS levels, could explain decreased proliferation and loss of differentiation potential. Hence, e-cigarettes present similar risk as combustible cigarettes with respect to tissue repair impairment.
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spelling pubmed-56601682017-11-01 Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation Shaito, A. Saliba, J. Husari, A. El-Harakeh, M. Chhouri, H. Hashem, Y. Shihadeh, A. El-Sabban, M. Sci Rep Article Electronic cigarettes (e-cigarettes) are promoted as low-risk alternatives to combustible cigarettes. However, the effects of chronic inhalation of potential toxicants emitted by ecigarettes remain largely unexamined. It is conceivable that smoking-induced chronic diseases result in cellular injury, in the absence of effective repair by stem cells. This study evaluates the effect of cigarette and e-cigarette aerosol extracts on the survival and differentiation of bone marrow-derived mesenchymal stem cells (MSCs). MSC growth and osteogenic differentiation were examined after exposure to smoke extracts. Data revealed detrimental effects of both cigarette and e-cigarette extracts on MSC morphology and growth. Levels and activity of alkaline phosphatase, an osteogenic marker, decreased and induction of osteoblastic differentiation was impaired. Both smoke extracts prevented osteogenic differentiation from progressing, evident by decreased expression of terminal osteogenic markers and mineralization. Elevated levels of reactive oxygen species (ROS) were detected in cells exposed to smoke extracts. Moreover, decreased differentiation potential was concomitant with severe down-regulation of Connexin 43 expression, leading to the loss of gap junction-mediated communication, which together with elevated ROS levels, could explain decreased proliferation and loss of differentiation potential. Hence, e-cigarettes present similar risk as combustible cigarettes with respect to tissue repair impairment. Nature Publishing Group UK 2017-10-27 /pmc/articles/PMC5660168/ /pubmed/29079789 http://dx.doi.org/10.1038/s41598-017-14634-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shaito, A.
Saliba, J.
Husari, A.
El-Harakeh, M.
Chhouri, H.
Hashem, Y.
Shihadeh, A.
El-Sabban, M.
Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title_full Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title_fullStr Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title_full_unstemmed Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title_short Electronic Cigarette Smoke Impairs Normal Mesenchymal Stem Cell Differentiation
title_sort electronic cigarette smoke impairs normal mesenchymal stem cell differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660168/
https://www.ncbi.nlm.nih.gov/pubmed/29079789
http://dx.doi.org/10.1038/s41598-017-14634-z
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