Cargando…

Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway

Background: Selenium (Se) can exert antioxidative activity and prevent the body from experiencing oxidative injury. Biogenic Se nanoparticles (SeNPs) synthesized by probiotics possess relatively strong chemical stability, high bioavailability, and low toxicity, this makes them potential Se supplemen...

Descripción completa

Detalles Bibliográficos
Autores principales: Xu, Chunlan, Qiao, Lei, Ma, Li, Guo, Yu, Dou, Xina, Yan, Shuqi, Zhang, Baohua, Roman, Alexandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593357/
https://www.ncbi.nlm.nih.gov/pubmed/31417254
http://dx.doi.org/10.2147/IJN.S199193
_version_ 1783430027662065664
author Xu, Chunlan
Qiao, Lei
Ma, Li
Guo, Yu
Dou, Xina
Yan, Shuqi
Zhang, Baohua
Roman, Alexandra
author_facet Xu, Chunlan
Qiao, Lei
Ma, Li
Guo, Yu
Dou, Xina
Yan, Shuqi
Zhang, Baohua
Roman, Alexandra
author_sort Xu, Chunlan
collection PubMed
description Background: Selenium (Se) can exert antioxidative activity and prevent the body from experiencing oxidative injury. Biogenic Se nanoparticles (SeNPs) synthesized by probiotics possess relatively strong chemical stability, high bioavailability, and low toxicity, this makes them potential Se supplements. Previously, we demonstrated that SeNPs synthesized by Lactobacillus casei ATCC 393 can alleviate hydrogen peroxide (H(2)O(2))-induced human and porcine intestinal epithelial cells' oxidative damage. However, the antioxidant mechanism remains unclear. Methods: The possible antioxidant mechanism and protective effect of SeNPs on intestinal epithelial permeability and mitochondrial function were evaluated by establishing an H(2)O(2)-induced oxidative damage model of human colon mucosal epithelial cells (NCM460) and conducting Nrf2 inhibitor interference experiments. Mitochondrial membrane potential (MMP), mitochondrial DNA content, adenosine triphosphate (ATP), ROS, and protein expression levels of Nrf2-related genes were determined. Mitochondrial ultrastructure was visualized by transmission electron microscopy. Results: An amount of 4 μg Se/mL of SeNPs synthesized by L. casei ATCC 393 alleviated increase of ROS, reduced ATP and MMP, and maintained intestinal epithelial permeability in NCM460 cells challenged by H(2)O(2). In addition, SeNPs improved the protein levels of Nrf2, HO-1, and NQO-1. Moreover, SeNPs attenuated the damage of mitochondrial ultrastructure caused by oxidative stress. Nrf2 inhibitor (ML385) abolished the regulatory effect of SeNPs on intracellular ROS production. Conclusion: Data suggest that biogenic SeNPs synthesized by L. casei ATCC 393 can protect the intestinal epithelial barrier function against oxidative damage by alleviating ROS-mediated mitochondrial dysfunction via Nrf2 signaling pathway. Biogenic SeNPs are an attractive candidate for potential Se supplement agent in preventing oxidative stress-related intestinal disease by targeting mitochondria.
format Online
Article
Text
id pubmed-6593357
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-65933572019-08-15 Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway Xu, Chunlan Qiao, Lei Ma, Li Guo, Yu Dou, Xina Yan, Shuqi Zhang, Baohua Roman, Alexandra Int J Nanomedicine Original Research Background: Selenium (Se) can exert antioxidative activity and prevent the body from experiencing oxidative injury. Biogenic Se nanoparticles (SeNPs) synthesized by probiotics possess relatively strong chemical stability, high bioavailability, and low toxicity, this makes them potential Se supplements. Previously, we demonstrated that SeNPs synthesized by Lactobacillus casei ATCC 393 can alleviate hydrogen peroxide (H(2)O(2))-induced human and porcine intestinal epithelial cells' oxidative damage. However, the antioxidant mechanism remains unclear. Methods: The possible antioxidant mechanism and protective effect of SeNPs on intestinal epithelial permeability and mitochondrial function were evaluated by establishing an H(2)O(2)-induced oxidative damage model of human colon mucosal epithelial cells (NCM460) and conducting Nrf2 inhibitor interference experiments. Mitochondrial membrane potential (MMP), mitochondrial DNA content, adenosine triphosphate (ATP), ROS, and protein expression levels of Nrf2-related genes were determined. Mitochondrial ultrastructure was visualized by transmission electron microscopy. Results: An amount of 4 μg Se/mL of SeNPs synthesized by L. casei ATCC 393 alleviated increase of ROS, reduced ATP and MMP, and maintained intestinal epithelial permeability in NCM460 cells challenged by H(2)O(2). In addition, SeNPs improved the protein levels of Nrf2, HO-1, and NQO-1. Moreover, SeNPs attenuated the damage of mitochondrial ultrastructure caused by oxidative stress. Nrf2 inhibitor (ML385) abolished the regulatory effect of SeNPs on intracellular ROS production. Conclusion: Data suggest that biogenic SeNPs synthesized by L. casei ATCC 393 can protect the intestinal epithelial barrier function against oxidative damage by alleviating ROS-mediated mitochondrial dysfunction via Nrf2 signaling pathway. Biogenic SeNPs are an attractive candidate for potential Se supplement agent in preventing oxidative stress-related intestinal disease by targeting mitochondria. Dove 2019-06-18 /pmc/articles/PMC6593357/ /pubmed/31417254 http://dx.doi.org/10.2147/IJN.S199193 Text en © 2019 Xu et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Xu, Chunlan
Qiao, Lei
Ma, Li
Guo, Yu
Dou, Xina
Yan, Shuqi
Zhang, Baohua
Roman, Alexandra
Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title_full Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title_fullStr Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title_full_unstemmed Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title_short Biogenic selenium nanoparticles synthesized by Lactobacillus casei ATCC 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via Nrf2 signaling-mediated mitochondrial pathway
title_sort biogenic selenium nanoparticles synthesized by lactobacillus casei atcc 393 alleviate intestinal epithelial barrier dysfunction caused by oxidative stress via nrf2 signaling-mediated mitochondrial pathway
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593357/
https://www.ncbi.nlm.nih.gov/pubmed/31417254
http://dx.doi.org/10.2147/IJN.S199193
work_keys_str_mv AT xuchunlan biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT qiaolei biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT mali biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT guoyu biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT douxina biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT yanshuqi biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT zhangbaohua biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway
AT romanalexandra biogenicseleniumnanoparticlessynthesizedbylactobacilluscaseiatcc393alleviateintestinalepithelialbarrierdysfunctioncausedbyoxidativestressvianrf2signalingmediatedmitochondrialpathway