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Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells

Mitochondrial dysfunction in tissue‐specific mesenchymal stem cells (MSCs) plays a critical role in cell fate and the morbidity of chronic inflammation‐associated bone diseases, such as periodontitis and osteoarthritis. However, there is still no effective method to cure chronic inflammation‐associa...

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Autores principales: Zhai, Qiming, Chen, Xin, Fei, Dongdong, Guo, Xiaoyan, He, Xiaoning, Zhao, Wanmin, Shi, Songtao, Gooding, John Justin, Jin, Fang, Jin, Yan, Li, Bei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811813/
https://www.ncbi.nlm.nih.gov/pubmed/34894103
http://dx.doi.org/10.1002/advs.202103839
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author Zhai, Qiming
Chen, Xin
Fei, Dongdong
Guo, Xiaoyan
He, Xiaoning
Zhao, Wanmin
Shi, Songtao
Gooding, John Justin
Jin, Fang
Jin, Yan
Li, Bei
author_facet Zhai, Qiming
Chen, Xin
Fei, Dongdong
Guo, Xiaoyan
He, Xiaoning
Zhao, Wanmin
Shi, Songtao
Gooding, John Justin
Jin, Fang
Jin, Yan
Li, Bei
author_sort Zhai, Qiming
collection PubMed
description Mitochondrial dysfunction in tissue‐specific mesenchymal stem cells (MSCs) plays a critical role in cell fate and the morbidity of chronic inflammation‐associated bone diseases, such as periodontitis and osteoarthritis. However, there is still no effective method to cure chronic inflammation‐associated bone diseases by physiologically restoring the function of mitochondria and MSCs. Herein, it is first found that chronic inflammation leads to excess Ca(2+) transfer from the endoplasmic reticulum to mitochondria, which causes mitochondrial calcium overload and further damage to mitochondria. Furthermore, damaged mitochondria continuously accumulate in MSCs due to the inhibition of mitophagy by activating the Wnt/β‐catenin pathway under chronic inflammatory conditions, impairing the differentiation of MSCs. Based on the mechanistic discovery, intracellular microenvironment (esterase and low pH)‐responsive nanoparticles are fabricated to capture Ca(2+) around mitochondria in MSCs to regulate MSC mitochondrial calcium flux against mitochondrial dysfunction. Furthermore, the same nanoparticles are able to deliver siRNA to MSCs to inhibit the Wnt/β‐catenin pathway and regulate mitophagy of the originally dysfunctional mitochondria. These precision‐engineered nanoparticles, referred to as “nanorepairers,” physiologically restore the function of mitochondria and MSCs, resulting in effective therapy for periodontitis and osteoarthritis. The concept can potentially be expanded to the treatment of other diseases via mitochondrial quality control intervention.
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spelling pubmed-88118132022-02-08 Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells Zhai, Qiming Chen, Xin Fei, Dongdong Guo, Xiaoyan He, Xiaoning Zhao, Wanmin Shi, Songtao Gooding, John Justin Jin, Fang Jin, Yan Li, Bei Adv Sci (Weinh) Research Articles Mitochondrial dysfunction in tissue‐specific mesenchymal stem cells (MSCs) plays a critical role in cell fate and the morbidity of chronic inflammation‐associated bone diseases, such as periodontitis and osteoarthritis. However, there is still no effective method to cure chronic inflammation‐associated bone diseases by physiologically restoring the function of mitochondria and MSCs. Herein, it is first found that chronic inflammation leads to excess Ca(2+) transfer from the endoplasmic reticulum to mitochondria, which causes mitochondrial calcium overload and further damage to mitochondria. Furthermore, damaged mitochondria continuously accumulate in MSCs due to the inhibition of mitophagy by activating the Wnt/β‐catenin pathway under chronic inflammatory conditions, impairing the differentiation of MSCs. Based on the mechanistic discovery, intracellular microenvironment (esterase and low pH)‐responsive nanoparticles are fabricated to capture Ca(2+) around mitochondria in MSCs to regulate MSC mitochondrial calcium flux against mitochondrial dysfunction. Furthermore, the same nanoparticles are able to deliver siRNA to MSCs to inhibit the Wnt/β‐catenin pathway and regulate mitophagy of the originally dysfunctional mitochondria. These precision‐engineered nanoparticles, referred to as “nanorepairers,” physiologically restore the function of mitochondria and MSCs, resulting in effective therapy for periodontitis and osteoarthritis. The concept can potentially be expanded to the treatment of other diseases via mitochondrial quality control intervention. John Wiley and Sons Inc. 2021-12-11 /pmc/articles/PMC8811813/ /pubmed/34894103 http://dx.doi.org/10.1002/advs.202103839 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhai, Qiming
Chen, Xin
Fei, Dongdong
Guo, Xiaoyan
He, Xiaoning
Zhao, Wanmin
Shi, Songtao
Gooding, John Justin
Jin, Fang
Jin, Yan
Li, Bei
Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title_full Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title_fullStr Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title_full_unstemmed Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title_short Nanorepairers Rescue Inflammation‐Induced Mitochondrial Dysfunction in Mesenchymal Stem Cells
title_sort nanorepairers rescue inflammation‐induced mitochondrial dysfunction in mesenchymal stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811813/
https://www.ncbi.nlm.nih.gov/pubmed/34894103
http://dx.doi.org/10.1002/advs.202103839
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