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Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs

Dicalcium silicate (Ca(2)SiO(4), C(2)S) has osteogenic potential but induces macrophagic inflammation. Mitochondrial function plays a vital role in macrophage polarization and macrophagic inflammation. The mitochondrial function of C(2)S-treated macrophages is still unclear. This study hypothesized:...

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Autores principales: Luo, Qianting, Li, Xingyang, Zhong, Wenchao, Cao, Wei, Zhu, Mingjing, Wu, Antong, Chen, Wanyi, Ye, Zhitong, Han, Qiao, Natarajan, Duraipandy, Pathak, Janak L, Zhang, Qingbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039510/
https://www.ncbi.nlm.nih.gov/pubmed/35480858
http://dx.doi.org/10.1093/rb/rbab075
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author Luo, Qianting
Li, Xingyang
Zhong, Wenchao
Cao, Wei
Zhu, Mingjing
Wu, Antong
Chen, Wanyi
Ye, Zhitong
Han, Qiao
Natarajan, Duraipandy
Pathak, Janak L
Zhang, Qingbin
author_facet Luo, Qianting
Li, Xingyang
Zhong, Wenchao
Cao, Wei
Zhu, Mingjing
Wu, Antong
Chen, Wanyi
Ye, Zhitong
Han, Qiao
Natarajan, Duraipandy
Pathak, Janak L
Zhang, Qingbin
author_sort Luo, Qianting
collection PubMed
description Dicalcium silicate (Ca(2)SiO(4), C(2)S) has osteogenic potential but induces macrophagic inflammation. Mitochondrial function plays a vital role in macrophage polarization and macrophagic inflammation. The mitochondrial function of C(2)S-treated macrophages is still unclear. This study hypothesized: (i) the C(2)S modulates mitochondrial function and autophagy in macrophages to regulate macrophagic inflammation, and (ii) C(2)S-induced macrophagic inflammation regulates osteogenesis. We used RAW264.7 cells as a model of macrophage. The C(2)S (75–150 μg/ml) extract was used to analyze the macrophagic mitochondrial function and macrophage-mediated effect on osteogenic differentiation of mouse bone marrow-derived mesenchymal stem cells (BMSCs). The results showed that C(2)S extract (150 μg/ml) induced TNF-α, IL-1β and IL-6 production in macrophages. C(2)S extract (150 μg/ml) enhanced reactive oxygen species level and intracellular calcium level but reduced mitochondrial membrane potential and ATP production. TEM images showed reduced mitochondrial abundance and altered the mitochondrial morphology in C(2)S (150 μg/ml)-treated macrophages. Protein level expression of PINK1, Parkin, Beclin1 and LC3 was upregulated but TOMM20 was downregulated. mRNA sequencing and KEGG analysis showed that C(2)S-induced differentially expressed mRNAs in macrophages were mainly distributed in the essential signaling pathways involved in mitochondrial function and autophagy. The conditioned medium from C(2)S-treated macrophage robustly promoted osteogenic differentiation in BMSCs. In conclusion, our results indicate mitochondrial dysfunction and autophagy as the possible mechanism of C(2)S-induced macrophagic inflammation. The promotion of osteogenic differentiation of BMSCs by the C(2)S-induced macrophagic inflammation suggests the potential application of C(2)S in developing immunomodulatory bone grafts.
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spelling pubmed-90395102022-04-26 Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs Luo, Qianting Li, Xingyang Zhong, Wenchao Cao, Wei Zhu, Mingjing Wu, Antong Chen, Wanyi Ye, Zhitong Han, Qiao Natarajan, Duraipandy Pathak, Janak L Zhang, Qingbin Regen Biomater Research Article Dicalcium silicate (Ca(2)SiO(4), C(2)S) has osteogenic potential but induces macrophagic inflammation. Mitochondrial function plays a vital role in macrophage polarization and macrophagic inflammation. The mitochondrial function of C(2)S-treated macrophages is still unclear. This study hypothesized: (i) the C(2)S modulates mitochondrial function and autophagy in macrophages to regulate macrophagic inflammation, and (ii) C(2)S-induced macrophagic inflammation regulates osteogenesis. We used RAW264.7 cells as a model of macrophage. The C(2)S (75–150 μg/ml) extract was used to analyze the macrophagic mitochondrial function and macrophage-mediated effect on osteogenic differentiation of mouse bone marrow-derived mesenchymal stem cells (BMSCs). The results showed that C(2)S extract (150 μg/ml) induced TNF-α, IL-1β and IL-6 production in macrophages. C(2)S extract (150 μg/ml) enhanced reactive oxygen species level and intracellular calcium level but reduced mitochondrial membrane potential and ATP production. TEM images showed reduced mitochondrial abundance and altered the mitochondrial morphology in C(2)S (150 μg/ml)-treated macrophages. Protein level expression of PINK1, Parkin, Beclin1 and LC3 was upregulated but TOMM20 was downregulated. mRNA sequencing and KEGG analysis showed that C(2)S-induced differentially expressed mRNAs in macrophages were mainly distributed in the essential signaling pathways involved in mitochondrial function and autophagy. The conditioned medium from C(2)S-treated macrophage robustly promoted osteogenic differentiation in BMSCs. In conclusion, our results indicate mitochondrial dysfunction and autophagy as the possible mechanism of C(2)S-induced macrophagic inflammation. The promotion of osteogenic differentiation of BMSCs by the C(2)S-induced macrophagic inflammation suggests the potential application of C(2)S in developing immunomodulatory bone grafts. Oxford University Press 2021-12-13 /pmc/articles/PMC9039510/ /pubmed/35480858 http://dx.doi.org/10.1093/rb/rbab075 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Luo, Qianting
Li, Xingyang
Zhong, Wenchao
Cao, Wei
Zhu, Mingjing
Wu, Antong
Chen, Wanyi
Ye, Zhitong
Han, Qiao
Natarajan, Duraipandy
Pathak, Janak L
Zhang, Qingbin
Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title_full Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title_fullStr Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title_full_unstemmed Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title_short Dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of BMSCs
title_sort dicalcium silicate-induced mitochondrial dysfunction and autophagy-mediated macrophagic inflammation promotes osteogenic differentiation of bmscs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039510/
https://www.ncbi.nlm.nih.gov/pubmed/35480858
http://dx.doi.org/10.1093/rb/rbab075
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